Chemistry | High school » Cengage Chemistry Catalog, Higher Education

Source: http://www.doksinet Source: http://www.doksinet Cengage Learning is a leading educational content, technology, and services company for the higher education and K-12, professional and library markets worldwide. The company provides superior content, personalized services and course-driven digital solutions that accelerate student engagement and transform the learning experience. Cengage Learning is headquartered in Boston, MA with operations in more than 20 countries around the world. For more, wwwcengagecom/about and wwwcengageasiacom Cengage Learning is Engaged with. Students – By engaging with you and listening to how you work best, we are creating products and solutions to fit your learning style and help keep you engaged – wherever you are. We are putting students first in the development of educational materials and are transforming the learning process to help you succeed. Educators – Faculty tell us that their job is to Engage Students. Our job is to help

Engaging your students means to advance, challenge and inspire them in the classroom and beyond. By working together to develop solutions with the end–user in mind, and supporting your efforts with unparalleled services and support, we can help you cultivate engaged learners, resulting in better outcomes. Librarians – Information must be used to be valuable. You are curators of authoritative material, and together, with our content and digital tools, we can help you to engage your users with the treasures of the library. Booksellers – We are engaged with booksellers through a variety of professional services and collaboration. Together we form a cohesive and flexible partnership for meeting mutually beneficial objectives. Source: http://www.doksinet Contents Chemistry Allied Health Chemistry������������������������������������������ 2 Analytical

Chemistry��������������������������������������������� 36 Biochemistry��������������������������������������������������������� 38 General Chemistry����������������������������������������������� 42 Inorganic Chemistry��������������������������������������������� 87 Introductory / Preparatory Chemistry������������������� 88 Liberal Arts Chemistry���������������������������������������� 104 Organic

Chemistry��������������������������������������������� 106 Physical Chemistry��������������������������������������������� 139 Spectroscopy����������������������������������������������������� 140 Combined Author/Title Index����������������������������� 142 Order form/pricelist is available upon request through Cengage Learning Representative. Special price requests for class adoption are subject to approval. Please contact your Cengage Learning Representative for details. Information contained in this catalog is correct at the time of printing. Prices are subject to change without prior notice. Source: http://www.doksinet CHEMISTRY ALLIED

HEALTH CHEMISTRY grading. • Section Quizzes--new section quizzes at the end of each of section test student understanding of the section. The quizzes test student understanding at the micro-level and reinforce key concepts. There are 356 section quizzes; total of 1, 252 questions. • Learning Focus--new feature called “Learning Focus”. Learning focuses are placed at the beginning of each section and provide students with insight into what each section is going to focus on and the associated learning outcomes for those sections. FEATURES GENERAL, ORGANIC, AND BIOLOGICAL CHEMISTRY, 7E H. Stephen Stoker, Weber State University Emphasizing the applications of chemistry and minimizing complicated mathematics, GENERAL, ORGANIC, AND BIOLOGICAL CHEMISTRY, 7E is written throughout to help students succeed in the course and master the biochemistry content so important to their future careers. The Six Edition’s clear explanations, visual support, and effective pedagogy combine to make

the text ideal for allied health majors. Early chapters focus on fundamental chemical principles while later chapters build on the foundations of these principles. Mathematics is introduced at point-of-use and only as needed. NEW TO THIS EDITION • The most powerful online learning solution for chemistry is better than ever. OWLv2 now has more flexible student and instructor functionality, new personalized study tools, enhanced integration with learning management systems, and improved analytics. For this course, OWLv2 also includes Quick Prep, an online short course to review key chemistry concepts and essential skills, new iPad-compatible visualizations, tutorials, and simulations, and new Adaptive Study Plans. In addition, Tutors, Visualizations and Simulations have been converted from Flash to HTML, allowing for easier navigation and streamlined 2 • OWLv2 is the most trusted online learning solution for chemistry. Featuring chemist-developed content, OWLv2 is the only system

designed to elevate thinking through Mastery Learning, allowing students to work at their own pace until they understand each concept and skill. Each time a student tries a problem, OWLv2 changes the, chemistry, values, and sometimes even the wording of the question to ensure students are learning the concepts and not cheating the system. With detailed, instant feedback and interactive learning resources, students get the help they need when they need it. Now with improved student and instructor tools and greater functionality, OWLv2 is more robust than ever. Discover the power of OWLv2 and take learning to a higher level. • Chemistry at-a-Glance features provide brief visual summaries of core chapter concepts to help students visualize difficult material. • Chemical Connection Boxes show chemistry as it relates to everyday life, highlighting its relevance to students’ future careers in the health and environmental fields. • A wide range of examples throughout the book help

students improve their problem-solving skills. • Early chapters focus on fundamental chemical principles; later chapters build on the foundation of these principles. • The book is fully integrated with the OWL online learning system, which saves instructors time and helps students master concepts and improve their grades. www.cengageasiacom Source: http://www.doksinet CONTENTS PART I: GENERAL CHEMISTRY.1 Basic Concepts About Matter.2 Measurements in Chemistry3 Atomic Structure and the Periodic Table.4 Chemical Bonding: The Ionic Bond Model.5 Chemical Bonding: The Covalent Bond Model.6 Chemical Calculations: Formula Masses, Moles, and Chemical Equations.7 Gases, Liquids, and Solids.8 Solutions9 Chemical Reactions.10 Acids, Bases, and Salts11 Nuclear Chemistry.PART II: ORGANIC CHEMISTRY12 Saturated Hydrocarbons.13 Unsaturated Hydrocarbons.14 Alcohols, Phenols, and Ethers15 Aldehydes and Ketones.16 Carboxylic Acids, Esters, and Other Acid Derivatives.17 Amines and Amides.PART III:

BIOLOGICAL CHEMISTRY18 Carbohydrates.19 Lipids20 Proteins21 Enzymes and Vitamins.22 Nucleic Acids23 Biochemical Energy Production.24 Carbohydrate Metabolism25 Lipid Metabolism.26 Protein MetabolismAnswers to Selected ExercisesIndex Glossary 2016, 1232pp, Hardback, 9781285853918 GENERAL, ORGANIC, AND BIOLOGICAL CHEMISTRY, HYBRID (WITH OWLV2 QUICK PREP FOR GENERAL CHEMISTRY PRINTED ACCESS CARD), 7E H. Stephen Stoker, Weber State University Emphasizing the applications of chemistry and minimizing complicated mathematics, GENERAL, ORGANIC, AND BIOLOGICAL CHEMISTRY is written throughout to help students succeed in the course and master the biochemistry content so important to their future careers. This Edition’s clear explanations, visual support, and effective pedagogy combine to make the text ideal for allied health majors. Early chapters focus on fundamental chemical principles while later chapters build on the foundations of these principles. Mathematics is introduced at

point-of-use and only as needed. NEW TO THIS EDITION • The most powerful online learning solution for chemistry is better than ever. OWLv2 now has more flexible student and instructor functionality, new personalized study tools, enhanced integration with learning management systems, and improved analytics. For this course, OWLv2 also includes Quick Prep, an online short course to review key chemistry concepts and essential skills, new iPad-compatible visualizations, tutorials, and simulations, and new Adaptive Study Plans. In addition, Tutors, Visualizations and Simulations have been converted from Flash to HTML, allowing for easier navigation and streamlined grading. www.cengageasiacom 3 Source: http://www.doksinet • Section Quizzes--new quick quizzes at the end of each of section test student understanding at the section level, and reinforce key concepts. There are 356 section quizzes; total of 1, 252 questions. • Learning Focus--new feature called “Learning Focus”.

Learning focuses are placed at the beginning of each section and provide students with insight into what each section is going to focus on and the associated learning outcomes for those sections. FEATURES • OWLv2 is the most trusted online learning solution for chemistry. Featuring chemist-developed content, OWLv2 is the only system designed to elevate thinking through Mastery Learning, allowing students to work at their own pace until they understand each concept and skill. Each time a student tries a problem, OWLv2 changes the, chemistry, values, and sometimes even the wording of the question to ensure students are learning the concepts and not cheating the system. With detailed, instant feedback and interactive learning resources, students get the help they need when they need it. Now with improved student and instructor tools and greater functionality, OWLv2 is more robust than ever. Discover the power of OWLv2 and take learning to a higher level. • Chemistry at-a-Glance

features provide brief visual summaries of core chapter concepts to help students visualize difficult material. • Chemical Connection Boxes show chemistry as it relates to everyday life, highlighting its relevance to students’ future careers in the health and environmental fields. • A wide range of examples throughout the book help students improve their problem-solving skills. • Early chapters focus on fundamental chemical principles; later chapters build on the foundation of these principles. • The book is fully integrated with the OWL online learning system, which saves instructors time and helps students master concepts and improve their grades. About Matter. 2 Measurements in Chemistry 3. Atomic Structure and the Periodic Table 4 Chemical Bonding: The Ionic Bond Model. 5 Chemical Bonding: The Covalent Bond Model. 6 Chemical Calculations: Formula Masses, Moles, and Chemical Equations. 7 Gases, Liquids, and Solids. 8 Solutions 9 Chemical Reactions 10 Acids, Bases, and

Salts. 11 Nuclear Chemistry PART II: ORGANIC CHEMISTRY.12 Saturated Hydrocarbons. 13 Unsaturated Hydrocarbons 14 Alcohols, Phenols, and Ethers. 15 Aldehydes and Ketones. 16 Carboxylic Acids, Esters, and Other Acid Derivatives. 17 Amines and Amides PART III: BIOLOGICAL CHEMISTRY.18 Carbohydrates 19 Lipids. 20 Proteins 21 Enzymes and Vitamins 22 Nucleic Acids. 23 Biochemical Energy Production 24. Carbohydrate Metabolism 25 Lipid Metabolism 26. Protein Metabolism Answers to Selected Exercises.Index Glossary 2016, 1040pp, Paperback, 9781305253070 CONTENTS PART I: GENERAL CHEMISTRY.1 Basic Concepts 4 www.cengageasiacom Source: http://www.doksinet INTRODUCTION TO GENERAL, ORGANIC AND BIOCHEMISTRY, 11E Frederick A. Bettelheim, Adelphi University; William H Brown, Beloit College; Mary K. Campbell, Mount Holyoke College; Shawn O. Farrell, Olympic Training Center This bestselling text continues to lead the way with a strong focus on current issues, pedagogically rich framework, wide

variety of medical and biological applications, visually dynamic art program, and exceptionally strong and varied end-of-chapter problems. Revised and updated throughout, the tenth edition now includes new biochemistry content, new Chemical Connections essays, new and revised problems, and more. Most end of chapter problems are now available in the OWL online learning system. NEW TO THIS EDITION • The most powerful online learning solution for chemistry is better than ever. OWLv2 now has more flexible student and instructor functionality, new personalized study tools, enhanced integration with learning management systems, and improved analytics. For this course, OWLv2 also includes Quick Prep, an online short course to review key chemistry concepts and essential skills, hundreds of new interactive end-of-chapter questions from the text, and new Adaptive Study Plans. In addition, Tutors, Visualizations and Simulations have been converted from Flash to HTML, allowing for easier

navigation and streamlined grading. • Features to highlight: Updated and new Chemical Connection boxes featuring the latest hot topics in general, organic and biochemistry. • New Challenge Problems--these problems test understanding of important concepts by building on material presented in earlier chapters. For example in chapter 4 the challenge problems draw of material introduced in chapters 1-4. • General Chemistry: Chapter 1--Emphasis on solving healthcare application conversion problems related to a clinical setting. Chapter 4, Chemical Reactions, introduces the various intricacies in writing and balancing chemical reactions before stoichiometry is introduced. This chapter includes the How To box, How to Balance a Chemical Equation, which illustrates a step-bystep method for balancing an equation. Twentythree new challenge problems were added • Expanded the list of common organic functional groups to include amides and presented a schematic of a tripeptide to show the

importance of amide bonds in the structure of polypeptides and proteins. Expanded the discussion of the reactions of phenols to include the oxidation of phenols to quinones and the use of the hydroquinone to quinone interconversion in blackand-white photography and continuing with role of Coenzyme Q (ubiquinone) in the respiratory chain as a carrier of electrons and concluding with the structure of vitamin K and its role in blood clotting. • Biochemistry--this edition introduces three of the newest RNA types to be discovered and there is a new section on epigenetics. FEATURES • OWLv2 is the most trusted online learning solution for chemistry. Featuring chemist-developed content, OWLv2 is the only system designed to elevate thinking through Mastery Learning, allowing students to work at their own pace until they understand each concept and skill. Each time a student tries a problem, OWLv2 changes the, chemistry, values, and sometimes even the wording of the question to ensure

students are learning the concepts and not cheating the system. With detailed, instant feedback and interactive learning resources, students get the help they need when they need it. Now with improved student and instructor tools and greater functionality, OWLv2 is more robust than ever. www.cengageasiacom 5 Source: http://www.doksinet Discover the power of OWLv2 and take learning to a higher level. • Problem-Solving Strategies: To help students organize the information to solve a problem, each chapter example includes a description of the strategy used to arrive at the solution. • Visual Impact: Many illustrations have heightened pedagogical impact. Figures such as Figures 64 (Henry’s Law) and 6.11 (electrolytic conductance) show the microscopic and macroscopic aspects of a topic under discussion. • Chemical Connections: More than 150 essays with photos describe applications of chemical concepts presented in the text, linking the chemistry to their real uses. In addition,

application boxes cover diverse topics such as diseases, drugs, and biochemical pathways. CONTENTS 1. Matter, Energy, and Measurement2 Atoms3 Chemical Bonds.4 Chemical Reactions5 Gases, Liquids, and Solids.6 Solutions and Colloids7 Reaction Rates and Chemical Equilibrium.8 Acids and Bases.9 Nuclear Chemistry10 Organic Chemistry.11 Alkanes12 Alkenes and Alkynes.13 Benzene and Its Derivatives14 Alcohols, Ethers, and Thiols.15 Chirality: The Handedness of Molecules.16 Amines17 Aldehydes and Ketones.18 Carboxylic Acids19 Carboxylic Anhydrides, Esters, and Amides.20 Carbohydrates.21 Lipids22 Proteins23 Enzymes.24 Chemical Communications: Neurotransmitters and Hormones.25 Nucleotides, Nucleic Acids, and Heredity.26 Gene Expression and Protein Synthesis.27 Bioenergetics: How the Body Converts Food to Energy.28 Specific Catabolic Pathways: Carbohydrate, Lipid, and Protein Metabolism.29 Biosynthetic Pathways30 Nutrition.31 Immunochemistry32 Body Fluids Appendix 1. Exponential NotationAppendix

2. Significant FiguresAnswers to In-Text and Odd-Numbered End-of-Chapter Problems. GlossaryCreditsIndex. LAB MANUAL FOR STOKER’S GENERAL, ORGANIC, AND BIOLOGICAL CHEMISTRY, 7TH, 7E H. Stephen Stoker, Weber State University Each experiment in this manual was selected to match topics in your textbook and includes an introduction, a procedure, a page of pre-lab exercises about the concepts the lab illustrates, and a report form. Some have a scenario that places the experiment in a real-world context. In addition, each experiment has a link to a set of references and helpful online resources. 2016, 448pp, Paperback, 9781305081093 2016, 1056pp, Hardback, 9781285869759 6 www.cengageasiacom Source: http://www.doksinet a wide range of possibilities to suit their lab. CONTENTS BASIC LABORATORY EXPERIMENTS FOR GENERAL, ORGANIC, AND BIOCHEMISTRY, 2E Joseph M. Landesberg, Adelphi University Focused, streamlined, and designed throughout to meet the needs of the one-term GOB Lab

course, this manual features 14 easy-to-follow experiments (6 general chemistry, 4 organic chemistry, and 4 biochemistry) that illustrate the key concepts that every allied health student must know. Clear directions help students complete labs successfully, while pre- and post-lab questions for every experiment test their ability to apply concepts. Preface.AcknowledgementsPractice Safe Laboratory.1 Laboratory Measurements2 Density Determination.3 Classes of Chemical Reactions4 Physical Properties of Chemicals: Melting Point, Sublimation, and Boiling Point.5 Factors Affecting Rate of Reactions.6 The Law of Chemical Equilibrium and the Le Chatelier Principle.7 pH and Buffer Solutions.8 Structure in Organic Compounds: Use of Molecular Models.9 Aspirin: Preparation and Properties (Acetylsalicylic Acid).10 Carbohydrates.11 Fats and Oils: Preparation and Properties of Soap.12 Separation of Amino Acids by Paper Chromotography.13 Isolation and Identification of Casein.14 EnzymesAppendix 1:

Use of the Laboratory Gas Burner.Appendix 2: List of Apparatus and Equipment in Student’s Locker. Appendix 3: List of Common Equipment and Material in the Laboratory.Appendix 4: Special Equipment and Chemical Preparations for Each Experiment. 2015, 240pp, Paperback, 9781285459653 NEW TO THIS EDITION • Labs have been updated with the most recent data and values in order to accurately reflect the changes in lab courses. Experiments 2 and 12 have been heavily revised, and includes new art. FEATURES • DESIGNED FOR NURSING AND HEALTH SCIENCE MAJORS. Focusing on the key concepts most important to allied health majors, this streamlined lab manual is ideal for the one-term General, Organic, and Biochemistry laboratory course. • CLEAR AND STRAIGHTFORWARD. Clear directions help students complete labs successfully. • A FOCUS ON APPLICATION. Pre- and post-lab questions for every experiment test the student’s ability to understand and apply concepts. • OPTIONS. Many labs include

multiple equipment and technique options to provide instructors with www.cengageasiacom 7 Source: http://www.doksinet • • GENERAL, ORGANIC, AND BIOCHEMISTRY, 2E An Applied Approach James Armstrong, City College of San Francisco Focusing on the needs of allied health and nursing majors, this engaging book is ideal for students who have had no prior exposure to chemistry. The author takes the time to explain how to do tasks that students find difficult, rather than just providing terse descriptions. Emphasizing problem-solving techniques without skipping steps and using terms students can grasp, the book takes the most direct path to biomolecules and metabolic processes, provides a wealth of worked examples to help students understand key chemical concepts, includes novel and relevant “Health Notes” in the margins, and weaves biological and medical applications throughout. • • • NEW TO THIS EDITION • The #1 online homework and learning system for chemistry,

OWLv2, is available for this textnow with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader™, a new eBook with apps and embedded video, audio, annotations, and activities. OWLv2 courses for Gen Chem, GOB, and Liberal Arts now include Quick Prep 8 • essential skills assignments that can be taken before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text and new iPad-compatible visualizations, tutorials, and simulations. The chapter on nuclear chemistry (formerly Chapter 16) has been moved to the

end of the material on general chemistry, becoming Chapter 8 in the second edition. To streamline the text, the following peripheral topics have been eliminated: heating and cooling curves, the ideal gas law, precipitation reactions, Le Châtelier’s principle, mass-energy conversion calculations, bombardment reactions and the production of radioisotopes, Markovnikov’s rule, the solubility of organic compounds in organic solvents, the structures and functions of steroids, and anabolic pathways. The sections on biologically important amines and on radioisotopes in medicine have been replaced by new end-of-chapter “Connections” essays covering much of the same material. Coverage of the moles and molar masses has been moved from Chapter 5 to the end of Chapter 2, allowing early exposure to this often-difficult concept. The topic sequence in Chapter 2 has been revised extensively, giving a more logical flow of subject matter. The electronic structure of atoms is now covered

immediately after the introduction to atoms, allowing uninterrupted coverage of atomic structure. The separate sections on the periodic table have been combined into a single section, which appears after the material on electronic structure. The material on chemical similarities has been compressed and moved to Chapter 3. The material on gas law computations, which was formerly placed in the appendices, has been streamlined and moved into Chapter 4. At the same time, the two sections on solubility have been moved from Chapter 4 to Chapter 5. The remaining sections of Chapter 4 have been edited to improve the flow of this chapter. These changes give a better topic balance between Chapters 2, 4 and 5. www.cengageasiacom Source: http://www.doksinet • Condensed structures for unbranched hydrocarbon chains are introduced in Chapter 5, simplifying the molecular structures required in the discussion of amphipathic compounds. • A discussion of the carbon cycle has been added to Chapter

6, following the introduction of combustion reactions. • The coverage of the properties of acids and bases in Chapter 7 has been simplified, with the elimination of subsections on the relationship between the pH of a solution and the molarity and strength of the acid or base in the solution. CONTENTS 1. MEASUREMENTS IN SCIENCE AND MEDICINE.11 Measuring size: distance, mass, and volume. 12 Measurements in science: precision and accuracy. 13 Metric units and their relationships. 14 Unit conversions and conversion factors. 15 Using multiple conversion factors. 16 Density, dosage, and other compound units1.7 Temperature Connections: Why Do We Struggle Against the Metric System?2. ATOMS, ELEMENTS, AND COMPOUNDS.21 Classifying matter: mixtures, compounds, and elements. 22 Atoms and atomic structure.23 Electron shells and valence electrons. 24 An introduction to the periodic table. 25 Isotopes and atomic weight 26 Moles 2.7 Compounds, chemical formulas, and moles Connections: The Elements

of Life.3 CHEMICAL BONDS.31 Covalent bonds and the octet rule 32 Double and triple bonds. 33 Electronegativity and polar bonds. 34 Naming covalent compounds 35 Ions and ionic compounds. 36 Writing formula for ionic compounds. 37 Naming ionic compounds 38 Polyatomic ions. 39 Recognizing ionic and molecular compounds. Connections: Nitrogen and Oxygen: A Remarkable Partnership.4 ENERGY AND PHYSICAL PROPERTIES.41 Heat and energy 4.2 The three states of matter 43 The properties of gases. 44 Gas law calculations 45 Attractive forces and the physical properties of matter. 46 Solutions and the dissolving process. 47 Electrolytes and dissociation. Connections: Temperature, Pressure, and Volume in Everyday Life.5 SOLUTION CONCENTRATION.51 Concentration 5.2 Solubility 53 The relationship between solubility and molecular structure. 54 Molarity 55 Osmosis, dialysis, and tonicity. 56 Equivalents 57 Dilution. Connections: Physiological Dehydration6 CHEMICAL REACTIONS.61 Physical changes and chemical

reactions. 62 Chemical equations 6.3 Mass relationships in a chemical reaction 64 Heats of reaction. 65 Combustion reactions and the carbon cycle. 66 Reaction rate and activation energy. 67 Chemical equilibrium Connections: Energy from Food.7 ACIDS AND BASES71 The self-ionization of water. 72 The pH scale 73 Properties of acids. 74 Properties of bases 75 Acid-base reactions. 76 Amphiprotic molecules and ions. 77 Buffers 78 The role of buffers in human physiology. Connections: Consequences of Blood pH Changes.8 NUCLEAR CHEMISTRY81 Nuclear symbols. 82 Writing nuclear equations 8.3 Energy and nuclear reactions84 Measuring radiation. 85 Radiation sources and shielding 86 Nuclear decay and half-life. 87 Nuclear fission and fusion. Connections: Diagnostic Imaging9 HYDROCARBONS: AN INTRODUCTION TO ORGANIC MOLECULES.91 The special properties of carbon. 92 Linear alkanes: the foundation of organic chemistry.93 Branched alkanes, cycloalkanes, and isomers. 94 Naming branched alkanes: the IUPAC

system. 95 Functional groups 9.6 Alkenes and alkynes 97 Cis and trans isomers of alkenes.98 Benzene and aromatic compounds 9.9 Properties of hydrocarbons Connections: High-Octane Hydrocarbons.10 HYDRATION, DEHYDRATION, AND ALCOHOLS.101 The hydration reaction. 102 Controlling the product: an introduction to enzymes. 103 Naming alcohols 104 The physical properties of alcohols. 105 Chirality in organic molecules. 106 The dehydration reaction 10.7 Phenols and thiols Connections: Alcohols for Drinking – Or Not.11 CARBONYL COMPOUNDS AND REDOX REACTIONS.111 Hydrogenation and dehydrogenation. 112 Oxidation and reduction reactions and the carbonyl group. 113 The naming and properties of aldehydes and ketones. 114 Other oxidation and reduction reactions. 115 Carboxylic acids. 116 Biological oxidations and reductions: the redox coenzymes. 117 Introduction to metabolic pathways. Connections: Fragrances and Flavors12 ORGANIC ACIDS AND BASES.121 Reactions of organic acids. 122 Decarboxylation

reactions 123 www.cengageasiacom 9 Source: http://www.doksinet Amines. 124 Acid-base reactions of amines 125 The physiological behavior of organic acids and bases. Connections: Messing With Your Mind: The Power of Tryptamines.13 CONDENSATION AND HYDROLYSIS REACTIONS.131 An introduction to condensation reactions: ethers. 132 Esterification, amidation, and phosphorylation. 133 Condensation polymers. 134 Hydrolysis 135 The effect of pH on the products of hydrolysis. 136 The ATP cycle. Connections: Common Pain Relievers14 PROTEINS.141 Amino acids 142 Peptide bonds and the secondary structure of a protein. 143 Side chain interactions and tertiary structure. 144 Protein denaturation. 145 Enzyme structure and function. 146 Sources and metabolism of amino acids. Connections: Enzyme Assays in Medicine15 CARBOHYDRATES.151 Monosaccharides 152 Isomeric forms of monosaccharides: anomers and enantiomers.153 Disaccharides and the glycosidic linkage. 154 Common disaccharides and polysaccharides.

155 Carbohydrate catabolism. Connections: The Importance of Blood Glucose.16 LIPIDS AND MEMBRANES161 Fatty acids and triglycerides. 162 Chemical reactions of triglycerides. 163 Catabolism of fatty acids. 164 Glycerophospholipids and cell membranes. 165 Concentration gradients and ATP formation. Connections: Brown Adipose Tissue and Uncouplers.17 NUCLEIC ACIDS, PROTEIN SYNTHESIS, AND HEREDITY.171 Nucleotides 17.2 Structures of nucleic acid 173 DNA replication 17.4 Transcription and RNA processing 175 Translation and the genetic code. 176 The mechanism of protein synthesis. 177 Mutations and genetic disorders. Connections: The Human Genome Project and Genetic Screening.Appendix A Mathematics Supplement.Appendix B Summary of Organic Functional Groups.Appendix C Answers to Selected Problems. 2015, 736pp, Hardback, 9781285430232 10 GENERAL, ORGANIC, AND BIOCHEMISTRY, HYBRID EDITION (WITH OWLV2 24-MONTHS PRINTED ACCESS CARD), 2E James Armstrong, City College of San Francisco Reflecting

Cengage Learning’s commitment to offering flexible teaching solutions and value for students and instructors, this new hybrid version features the instructional presentation found in the printed text while delivering all the end-of chapter exercises online in OWLv2, the leading online learning system for chemistry. The resulta briefer printed text that engages students online! Help your students improve their grades and understanding of concepts with this value-packed Hybrid Edition. An access code to OWLV2 WITH MINDTAP READER, is included with the text, providing students with powerful online resources that include tutorials, simulations, randomized homework questions, videos, a complete interactive electronic version of the textbook, and more! Focusing on the needs of allied health and nursing majors, this engaging book is ideal for students who have had no prior exposure to chemistry. The author takes the time to explain how to do tasks that students find difficult, rather than

just providing terse descriptions. Emphasizing problem-solving techniques without skipping steps and using terms students can grasp, the book takes the most direct path to biomolecules and metabolic processes, provides a wealth of worked examples to help students understand key chemical concepts, includes novel and relevant “Health Notes” in the margins, and weaves biological and medical applications throughout. www.cengageasiacom Source: http://www.doksinet NEW TO THIS EDITION • The #1 online homework and learning system for chemistry, OWLv2, is available for this textnow with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader™, a new

eBook with apps and embedded video, audio, annotations, and activities. OWLv2 courses for Gen Chem, GOB, and Liberal Arts now include Quick Prep essential skills assignments that can be taken before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text and new iPad-compatible visualizations, tutorials, and simulations. • The chapter on nuclear chemistry (formerly Chapter 16) has been moved to the end of the material on general chemistry, becoming Chapter 8 in the second edition. • To streamline the text, the following peripheral topics have been eliminated: heating and cooling curves, the ideal gas law, precipitation reactions, Le Châtelier’s principle, mass-energy conversion calculations, bombardment reactions and the production of radioisotopes, Markovnikov’s rule, the solubility of organic compounds in organic solvents, the

structures and functions of steroids, and anabolic pathways. • The sections on biologically important amines and on radioisotopes in medicine have been replaced by new end-of-chapter “Connections” essays covering much of the same material. • Coverage of the moles and molar masses has been moved from Chapter 5 to the end of Chapter 2, allowing early exposure to this often-difficult concept. • The topic sequence in Chapter 2 has been revised extensively, giving a more logical flow of subject matter. The electronic structure of atoms is now covered immediately after the introduction to • • • • atoms, allowing uninterrupted coverage of atomic structure. The separate sections on the periodic table have been combined into a single section, which appears after the material on electronic structure. The material on chemical similarities has been compressed and moved to Chapter 3. The material on gas law computations, which was formerly placed in the appendices, has been

streamlined and moved into Chapter 4. At the same time, the two sections on solubility have been moved from Chapter 4 to Chapter 5. The remaining sections of Chapter 4 have been edited to improve the flow of this chapter. These changes give a better topic balance between Chapters 2, 4 and 5. Condensed structures for unbranched hydrocarbon chains are introduced in Chapter 5, simplifying the molecular structures required in the discussion of amphipathic compounds. A discussion of the carbon cycle has been added to Chapter 6, following the introduction of combustion reactions. The coverage of the properties of acids and bases in Chapter 7 has been simplified, with the elimination of subsections on the relationship between the pH of a solution and the molarity and strength of the acid or base in the solution. CONTENTS 1. MEASUREMENTS IN SCIENCE AND MEDICINE Measuring size: distance, mass, and volume. Measurements in science: precision and accuracy. Metric units and their relationships.

Unit conversions and conversion factors. Using multiple conversion factors. Density, dosage, and other compound unitsTemperature. Connections: Why Do We Struggle Against the Metric System?2. ATOMS, ELEMENTS, AND COMPOUNDS.Classifying matter: mixtures, compounds, and elements. Atoms and atomic structureElectron shells and valence electrons. An introduction to the periodic table Isotopes and atomic weight. Moles Compounds, chemical formulas, and moles. Connections: The Elements of Life.3 CHEMICAL BONDSCovalent bonds and the octet rule. Double and triple bonds. Electronegativity and polar bonds Naming covalent compounds. Ions and ionic compounds Writing formula for ionic compounds. Naming ionic www.cengageasiacom 11 Source: http://www.doksinet compounds. Polyatomic ions Recognizing ionic and molecular compounds. Connections: Nitrogen and Oxygen: A Remarkable Partnership.4 ENERGY AND PHYSICAL PROPERTIES.Heat and energy The three states of matter. The properties of gases Gas law

calculations. Attractive forces and the physical properties of matter. Solutions and the dissolving process. Electrolytes and dissociation Connections: Temperature, Pressure, and Volume in Everyday Life.5 SOLUTION CONCENTRATION Concentration. Solubility The relationship between solubility and molecular structure. Molarity Osmosis, dialysis, and tonicity. Equivalents Dilution. Connections: Physiological Dehydration6 CHEMICAL REACTIONS.Physical changes and chemical reactions. Chemical equations Mass relationships in a chemical reaction. Heats of reaction. Combustion reactions and the carbon cycle.Reaction rate and activation energy Chemical equilibrium. Connections: Energy from Food7 ACIDS AND BASES.The self-ionization of water The pH scale. Properties of acids Properties of bases. Acid-base reactions Amphiprotic molecules and ions. Buffers The role of buffers in human physiology. Connections: Consequences of Blood pH Changes.8 NUCLEAR CHEMISTRYNuclear symbols. Writing nuclear equations

Energy and nuclear reactions. Measuring radiation Radiation sources and shielding. Nuclear decay and half-life Nuclear fission and fusion. Connections: Diagnostic Imaging.9 HYDROCARBONS: AN INTRODUCTION TO ORGANIC MOLECULES.The special properties of carbon. Linear alkanes: the foundation of organic chemistry.Branched alkanes, cycloalkanes, and isomers. Naming branched alkanes: the IUPAC system. Functional groups Alkenes and alkynes Cis and trans isomers of alkenes. Benzene and aromatic compounds. Properties of hydrocarbons Connections: High-Octane Hydrocarbons.10 HYDRATION, DEHYDRATION, AND ALCOHOLS. The hydration reaction. Controlling the product: an introduction to enzymes. Naming alcohols The physical properties of alcohols. Chirality in organic molecules.The dehydration reaction Phenols and thiols. Connections: Alcohols for Drinking – Or Not.11 CARBONYL COMPOUNDS AND REDOX REACTIONS.Hydrogenation and dehydrogenation 12 Oxidation and reduction reactions and the carbonyl group.

The naming and properties of aldehydes and ketones. Other oxidation and reduction reactions. Carboxylic acids Biological oxidations and reductions: the redox coenzymes. Introduction to metabolic pathways. Connections: Fragrances and Flavors.12 ORGANIC ACIDS AND BASES Reactions of organic acids. Decarboxylation reactions. Amines Acid-base reactions of amines The physiological behavior of organic acids and bases. Connections: Messing With Your Mind: The Power of Tryptamines.13 CONDENSATION AND HYDROLYSIS REACTIONS.An introduction to condensation reactions: ethers. Esterification, amidation, and phosphorylation. Condensation polymers. Hydrolysis The effect of pH on the products of hydrolysis. The ATP cycle Connections: Common Pain Relievers.14 PROTEINSAmino acids. Peptide bonds and the secondary structure of a protein. Side chain interactions and tertiary structure. Protein denaturation Enzyme structure and function. Sources and metabolism of amino acids. Connections: Enzyme Assays in

Medicine15 CARBOHYDRATES.Monosaccharides Isomeric forms of monosaccharides: anomers and enantiomers. Disaccharides and the glycosidic linkage. Common disaccharides and polysaccharides. Carbohydrate catabolism. Connections: The Importance of Blood Glucose.16 LIPIDS AND MEMBRANESFatty acids and triglycerides. Chemical reactions of triglycerides Catabolism of fatty acids. Glycerophospholipids and cell membranes. Concentration gradients and ATP formation. Connections: Brown Adipose Tissue and Uncouplers.17 NUCLEIC ACIDS, PROTEIN SYNTHESIS, AND HEREDITY.Nucleotides Structures of nucleic acids. DNA replication Transcription and RNA processing. Translation and the genetic code. The mechanism of protein synthesis. Mutations and genetic disorders Connections: The Human Genome Project and Genetic Screening.Appendix A: Mathematics Supplement.Appendix B: Summary of Organic Functional Groups.Appendix C: Answers to Selected Problems. 2015, 688pp, Paperback, 9781285461434 www.cengageasiacom

Source: http://www.doksinet CHEMISTRY FOR TODAY, 8E General, Organic and Biochemistry, International Edition Spencer L. Seager, Weber State University; Michael R Slabaugh, Weber State University Distinguished by its superior allied health focus and integration of technology, Seager and Slabaugh’s CHEMISTRY FOR TODAY: GENERAL, ORGANIC, and BIOCHEMISTRY, 8E, International Edition meets students’ needs through diverse applications, examples, boxes, interactive technology tools, and, new to this edition, real life case studies. CHEMISTRY FOR TODAY: GENERAL, ORGANIC, and BIOCHEMISTRY, 8E, International Edition dispels students’ inherent fear of chemistry and instills an appreciation for the role chemistry plays in our daily lives through a rich pedagogical structure and an accessible writing style with lucid explanations. In addition, the book provides greater support in both problem-solving and critical-thinking skills--the skills necessary for student success. By demonstrating

the importance of chemistry concepts to students’ future careers, the authors not only help students set goals, but also help them focus on achieving them. NEW TO THIS EDITION • CASE STUDIES/CASE STUDY FOLLOW UPS: New Case Studies open each chapter with real life scenarios that students may encounter at home and at work. Each case study incorporates critical chemistry concepts from the chapter in an exciting real life scenario in which the reader feels as if they are a part of the experience. The case studies require the student to make a decision about what they would do if they were in that situation. A follow up to each Case Study appears at the end of each chapter. • ASK THE EXPERT: Featured on both the book cover and woven throughout the text the “Ask the Expert” boxes begin with important questions about nutrition and fitness as related to chemistry-questions that students need to ask and need to know the answers to. The “Ask the Expert” questions and answers are

written by CNN Doctor Melina D. Jampolis--one of the leading Nutrition and Fitness experts in the country. • NEW END-OF-CHAPTER EXERCISES: A significant number of the end-of-chapter questions are new. • ENHANCED OWL (ONLINE WEB LEARNING) INTEGRATION: For CHEMISTRY FOR TODAY: GENERAL, ORGANIC, and BIOCHEMISTRY, 8E, International Edition, OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes Student Self-Assessments, Interactive Examples from the text, the interactive customizable Cengage YouBook, a customizable iPad-compatible multimedia eBook, and an optional Solutions Manual eBook. FEATURES • A UNIQUE AND INSTRUCTIVE ART PROGRAM: “Talking Labels” in the art itself walk students through each figure, pointing out what they need to see. Explanations of figures are incorporated

into the art, rather than appearing in the caption, to help students follow processes and understand exactly what is happening within each figure without having to go back and forth between figure and caption. • STUDENT-FOCUSED BOXED FEATURES: New “Ask the Expert” boxes written by CNN Nutrition and Fitness Expert Melina D. Jampolis, MD discuss important questions and answers about nutrition and fitness as related to chemistry; “At the Counter” boxes focus on drugs and products found on drugstore shelves and at the pharmacy; “Chemistry Around Us” boxes present everyday www.cengageasiacom 13 Source: http://www.doksinet • • • • applications of chemistry; and updated “Chemistry and Your Health” boxes relate to students’ health and the health of the patients that they may care for in their future roles as a part of the allied health work force. A WEALTH OF END-OF-CHAPTER EXERCISES: The book’s wide range of end-of-chapter exercises include “Additional

Exercises” that are not tied to a specific section and often consist of problems that integrate several concepts and “Chemistry for Thought” exercises that focus on conceptual and cumulative questions and ask students to apply what they have learned to a particular cumulative question. ALLIED HEALTH CONNECTION: An “AlliedHealth Exam Connection” section follows each chapter’s end-of-chapter exercises and includes chemistry questions found on entrance examinations used to screen applicants applying to Allied-Health professional programs. INTEGRATED LEARNING OBJECTIVES: The book’s Learning Objectives are integrated throughout each chapter and within the summary to help students focus on the chapter’s key skills and concepts. LEARNING CHECKS: These short, self-check exercises follow the book’s worked-out examples and discussions of key or difficult concepts to help students assess their understanding. CONTENTS 1. Matter, Measurements, and Calculations2 Atoms and

Molecules.3 Electronic Structure and the Periodic Law.4 Forces Between Particles5 Chemical Reactions.6 The States of Matter7 Solutions and Colloids.8 Reaction Rates and Equilibrium9 Acids, Bases, and Salts.10 Radioactivity and Nuclear Processes.11 Organic Compounds: Alkanes.12 Unsaturated Hydrocarbons13 Alcohols, Phenols, and Ethers.14 Aldehydes and Ketones.15 Carboxylic Acids and Esters16 Amines and Amides.17 Carbohydrates18 Lipids.19 Proteins20 Enzymes21 Nucleic Acids and Protein Synthesis.22 Nutrition and Energy for Life.23 Carbohydrate Metabolism24 Lipid and Amino Acid Metabolism.25 Body FluidsAppendix A: The International System of Measurements. Appendix B: Answers to Even-Numbered End- 14 of-Chapter Exercises.Appendix C: Solutions to Learning Checks.GlossaryIndex 2014, 960pp, Paperback, 9781133604334 CHEMISTRY FOR TODAY, 8E General Organic and Biochemistry, Hybrid Edition (with OWLv2 with MindTap Reader 24-Month Printed Access Card) Spencer L. Seager, Weber State University;

Michael R Slabaugh, Weber State University Reflecting Cengage Learning’s commitment to offering flexible teaching solutions and value for students and instructors, this new hybrid version features the instructional presentation found in the printed text while delivering all the end-of chapter exercises online in OWL, the leading online learning system for chemistry. The resulta briefer printed text that engages students online! Distinguished by its superior allied health focus and integration of technology, The Hybrid Edition with MindTap Reader of Seager and Slabaugh’s CHEMISTRY FOR TODAY: GENERAL, ORGANIC, and BIOCHEMISTRY 8e meets students’ needs through diverse applications, examples, boxes, interactive technology tools, and, new to this edition, real life case studies. CHEMISTRY FOR TODAY dispels students’ inherent fear of chemistry and instills an appreciation for the role chemistry plays in our daily lives through a rich pedagogical structure and an accessible writing

style with lucid explanations. In addition, the book provides greater support in both problem-solving and critical-thinking skillsthe skills necessary for student success. By demonstrating the importance of chemistry www.cengageasiacom Source: http://www.doksinet concepts to students’ future careers, the authors not only help students set goals, but also help them focus on achieving them. NEW TO THIS EDITION • CASE STUDIES/CASE STUDY FOLLOW UPS: New Case Studies open each chapter with real life scenarios that students may encounter at home and at work. Each case study incorporates critical chemistry concepts from the chapter in an exciting real life scenario in which the reader feels as if they are a part of the experience. The case studies require the student to make a decision about what they would do if they were in that situation. A follow up to each Case Study appears at the end of each chapter. • ASK AN EXPERT: Featured on both the book cover and woven throughout the

text the “Ask An Expert” boxes begin with important questions about nutrition and fitness as related to chemistry questions that students need to ask and need to know the answers to. The “Ask an Expert” questions and answers are written by CNN Doctor Melina B. Jampolisone of the leading Nutrition and Fitness experts in the country. • NEW END-OF-CHAPTER EXERCISES: A significant number of the end-of-chapter questions are new. • ENHANCED OWL (ONLINE WEB LEARNING) INTEGRATION: For the Eighth Edition, OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes Student Self-Assessments, Interactive Examples from the text, and more. It also includes MindTap Reader. MindTap Reader is a free upgrade to existing readers in Cengage’ s existing digital platforms offering significant new

functionality while also preparing the platforms to take advantage of future MindTap services. FEATURES • • • • • into the art, rather than appearing in the caption, to help students follow processes and understand exactly what is happening within each figure without having to go back and forth between figure and caption. STUDENT-FOCUSED BOXED FEATURES: New “Ask An Expert” boxes written by CNN Nutrition and Fitness Expert Melina B. Jampolis, MD discuss important questions and answers about nutrition and fitness as related to chemistry; “At the Counter” boxes focus on drugs and products found on drugstore shelves and at the pharmacy; “Chemistry Around Us” boxes present everyday applications of chemistry; and updated “Chemistry and Your Health” boxes relate to students’ health and the health of the patients that they may care for in their future roles as a part of the allied health work force. A WEALTH OF END-OF-CHAPTER EXERCISES: The book’s wide range

of end-of-chapter exercises include “Additional Exercises” that are not tied to a specific section and often consist of problems that integrate several concepts and “Chemistry for Thought” exercises that focus on conceptual and cumulative questions and ask students to apply what they have learned to a particular cumulative question. ALLIED HEALTH CONNECTION: An “AlliedHealth Exam Connection” section follows each chapter’s end-of-chapter exercises and includes chemistry questions found on entrance examinations used to screen applicants applying to Allied-Health professional programs. INTEGRATED LEARNING OBJECTIVES: The book’s Learning Objectives are integrated throughout each chapter and within the summary to help students focus on the chapter’s key skills and concepts. LEARNING CHECKS: These short, self-check exercises follow the book’s worked-out examples and discussions of key or difficult concepts to help students assess their understanding. CONTENTS • A

UNIQUE AND INSTRUCTIVE ART PROGRAM: “Talking Labels” in the art itself walk students through each figure, pointing out what they need to see. Explanations of figures are incorporated 1. Matter, Measurements, and Calculations2 Atoms and Molecules.3 Electronic Structure and the Periodic Law.4 Forces Between Particles5 Chemical Reactions.6 The States of Matter7 Solutions www.cengageasiacom 15 Source: http://www.doksinet and Colloids.8 Reaction Rates and Equilibrium9 Acids, Bases, and Salts.10 Radioactivity and Nuclear Processes.11 Organic Compounds: Alkanes.12 Unsaturated Hydrocarbons13 Alcohols, Phenols, and Ethers.14 Aldehydes and Ketones.15 Carboxylic Acids and Esters16 Amines and Amides.17 Carbohydrates18 Lipids.19 Proteins20 Enzymes21 Nucleic Acids and Protein Synthesis.22 Nutrition and Energy for Life.23 Carbohydrate Metabolism24 Lipid and Amino Acid Metabolism.25 Body FluidsAppendix A: The International System of Measurements. Appendix B: Answers to Even-Numbered

Endof-Chapter Exercises.Appendix C: Solutions to Learning Checks.GlossaryIndex 2014, 784pp, Paperback, 9781285185972 INTRODUCTORY CHEMISTRY FOR TODAY, INTERNATIONAL EDITION, 8E Spencer L. Seager, Weber State University; Michael R Slabaugh, Weber State University Distinguished by its superior allied health focus and integration of technology, Seager and Slabaugh’s INTRODUCTORY CHEMISTRY FOR TODAY, 8E, International Edition meets students’ needs through diverse applications, examples, boxes, interactive technology tools, and -- new to this edition -- real life case studies. The Eighth Edition dispels students’ inherent fear of chemistry and instills an appreciation for the role chemistry plays in our daily lives through a rich pedagogical structure and an accessible writing style with lucid explanations. In addition, the book provides greater support in both 16 problem-solving and critical-thinking skills--the skills necessary for student success. By demonstrating the

importance of chemistry concepts to students’ future careers, the authors not only help students set goals, but also help them focus on achieving them. NEW TO THIS EDITION • CASE STUDIES/CASE STUDY FOLLOW UPS: New Case Studies open each chapter with real life scenarios that students may encounter at home and at work. Each case study incorporates critical chemistry concepts from the chapter in an exciting real life scenario in which the reader feels as if they are a part of the experience. The case studies require the student to make a decision about what they would do if they were in that situation. A follow up to each Case Study appears at the end of each chapter. • ASK THE EXPERT: Featured on both the book cover and woven throughout the text the “Ask the Expert” boxes begin with important questions about nutrition and fitness as related to chemistry-questions that students need to ask and need to know the answers to. The “Ask the Expert” questions and answers are

written by CNN Doctor Melina D. Jampolis--one of the leading Nutrition and Fitness experts in the country. • NEW END-OF-CHAPTER EXERCISES: A significant number of the end-of-chapter questions are new. • ENHANCED OWL (ONLINE WEB LEARNING) INTEGRATION: For the Eighth Edition, OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes Student Self-Assessments, Interactive Examples from the text, the interactive customizable Cengage YouBook, a customizable iPad-compatible multimedia eBook, and an optional Solutions Manual eBook. FEATURES • A UNIQUE AND INSTRUCTIVE ART PROGRAM: “Talking Labels” in the art itself walk students through each figure, pointing out what they need www.cengageasiacom Source: http://www.doksinet • • • • • to see. Explanations of figures are

incorporated into the art, rather than appearing in the caption, to help students follow processes and understand exactly what is happening within each figure without having to go back and forth between figure and caption. STUDENT-FOCUSED BOXED FEATURES: New “Ask the Expert” boxes written by CNN Nutrition and Fitness Expert Melina D. Jampolis, MD discuss important questions and answers about nutrition and fitness as related to chemistry; “At the Counter” boxes focus on drugs and products found on drugstore shelves and at the pharmacy; “Chemistry Around Us” boxes present everyday applications of chemistry; and updated “Chemistry and Your Health” boxes relate to students’ health and the health of the patients that they may care for in their future roles as a part of the allied health work force. A WEALTH OF END-OF-CHAPTER EXERCISES: The book’s wide range of end-of-chapter exercises include “Additional Exercises” that are not tied to a specific section and often

consist of problems that integrate several concepts and “Chemistry for Thought” exercises that focus on conceptual and cumulative questions and ask students to apply what they have learned to a particular cumulative question. ALLIED HEALTH CONNECTION: An “AlliedHealth Exam Connection” section follows each chapter’s end-of-chapter exercises and includes chemistry questions found on entrance examinations used to screen applicants applying to Allied-Health professional programs. INTEGRATED LEARNING OBJECTIVES: The book’s Learning Objectives are integrated throughout each chapter and within the summary to help students focus on the chapter’s key skills and concepts. LEARNING CHECKS: These short, self-check exercises follow the book’s worked-out examples and discussions of key or difficult concepts to help students assess their understanding. CONTENTS 1. Matter, Measurements, and Calculations2 Atoms and Molecules.3 Electronic Structure and the Periodic Law.4 Forces Between

Particles5 Chemical Reactions.6 The States of Matter7 Solutions and Colloids.8 Reaction Rates and Equilibrium9 Acids, Bases, and Salts.10 Radioactivity and Nuclear Processes.11 Organic Compounds: Alkanes.12 Unsaturated Hydrocarbons13 Alcohols, Phenols, and Ethers.14 Aldehydes and Ketones.15 Carboxylic Acids and Esters16 Amines and Amides.17 Carbohydrates18 Lipids.19 Proteins20 Enzymes21 Nucleic Acids and Protein Synthesis.22 Nutrition and Energy for Life.23 Carbohydrate Metabolism24 Lipid and Amino Acid Metabolism.25 Body FluidsAppendix A: The International System of Measurements. Appendix B: Answers to Even-Numbered Endof-Chapter Exercises.Appendix C: Solutions to Learning Checks.GlossaryIndex 2014, 528pp, Paperback, 9781133605119 ORGANIC AND BIOCHEMISTRY FOR TODAY, INTERNATIONAL EDITION, 8E Spencer L. Seager, Weber State University; Michael R Slabaugh, Weber State University Distinguished by its superior allied health focus and integration of technology, Seager and Slabaugh’s

ORGANIC AND BIOCHEMISTRY FOR TODAY, 8E, International Edition meets students’ needs through diverse applications, examples, boxes, interactive technology tools, and -- new to this edition -- real life case studies. The Eighth Edition dispels students’ inherent fear of chemistry and instills an appreciation for the role chemistry plays in our daily lives through a rich pedagogical structure and an accessible writing style with lucid www.cengageasiacom 17 Source: http://www.doksinet explanations. In addition, the book provides greater support in both problem-solving and critical-thinking skills--the skills necessary for student success. By demonstrating the importance of chemistry concepts to students’ future careers, the authors not only help students set goals, but also help them focus on achieving them. NEW TO THIS EDITION • CASE STUDIES AND CASE STUDY FOLLOW UPS: New Case Studies open each chapter with real life scenarios that students may encounter at home and at work.

Each case study incorporates critical chemistry concepts from the chapter in an exciting real life scenario in which readers feel as if they are a part of the experience. The case studies require students to make a decision about what they would do if they were in that situation. A follow up to each Case Study appears at the end of each chapter. • “ASK THE EXPERT” BOXES: Featured on both the book cover and woven throughout the text the “Ask the Expert” boxes begin with important questions about nutrition and fitness as related to chemistry--questions that students need to ask and need to know the answers to. The “Ask the Expert” questions and answers are written by CNN Doctor Melina D. Jampolis--one of the leading Nutrition and Fitness experts in the country. • NEW END-OF-CHAPTER EXERCISES: A significant number of the end-of-chapter questions are new. • ENHANCED OWL (ONLINE WEB LEARNING) INTEGRATION: For the Eighth Edition, OWL now includes more parameterized

end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes Student Self-Assessments, Interactive Examples from the text, the interactive customizable Cengage YouBook, a customizable iPad-compatible multimedia eBook, and an optional Solutions Manual eBook. FEATURES • • • • CONTENTS • A UNIQUE AND INSTRUCTIVE ART PROGRAM: “Talking Labels” in the art itself walk students 18 • through each figure, pointing out what they need to see. Explanations of figures are incorporated into the art, rather than appearing in the caption, to help students follow processes and understand exactly what is happening within each figure without having to go back and forth between figure and caption. STUDENT-FOCUSED BOXED FEATURES: New “Ask the Expert” boxes written by CNN Nutrition and Fitness Expert Melina D. Jampolis, MD

discuss important questions and answers about nutrition and fitness as related to chemistry; “At the Counter” boxes focus on drugs and products found on drugstore shelves and at the pharmacy; “Chemistry Around Us” boxes present everyday applications of chemistry; and updated “Chemistry and Your Health” boxes relate to students’ health and the health of the patients that they may care for in their future roles as a part of the allied health work force. A WEALTH OF END-OF-CHAPTER EXERCISES: The book’s wide range of end-of-chapter exercises include “Additional Exercises” that are not tied to a specific section and often consist of problems that integrate several concepts and “Chemistry for Thought” exercises that focus on conceptual and cumulative questions and ask students to apply what they have learned to a particular cumulative question. ALLIED HEALTH CONNECTION: An “AlliedHealth Exam Connection” section follows each chapter’s end-of-chapter exercises and

includes chemistry questions found on entrance examinations used to screen applicants applying to Allied-Health professional programs. INTEGRATED LEARNING OBJECTIVES: The book’s Learning Objectives are integrated throughout each chapter and within the summary to help students focus on the chapter’s key skills and concepts. LEARNING CHECKS: These short, self-check exercises follow the book’s worked-out examples and discussions of key or difficult concepts to help students assess their understanding. 1. Organic Compounds: Alkanes2 Unsaturated Hydrocarbons.3 Alcohols, Phenols, and Ethers4 www.cengageasiacom Source: http://www.doksinet Aldehydes and Ketones.5 Carboxylic Acids and Esters.6 Amines and Amides7 Carbohydrates8 Lipids.9 Proteins10 Enzymes11 Nucleic Acids and Protein Synthesis.12 Nutrition and Energy for Life.13 Carbohydrate Metabolism14 Lipid and Amino Acid Metabolism.15 Body FluidsAppendix A: The International System of Measurements. Appendix B: Answers to

Even-Numbered Endof-Chapter Exercises.Appendix C: Solutions to Learning Checks.GlossaryIndex 2014, 544pp, Paperback, 9781133607496 NEW TO THIS EDITION • Updated and thoroughly reviewed labs. FEATURES • ACCURATE AND CLASS-TESTED. The Eighth Edition includes 15 general chemistry and 20 organic/biochemistry safety-scale laboratory experiments--all thoroughly class-tested--that effectively illustrate the main text’s key concepts. • A KEY CONCEPT FOCUS: The manual’s blend of laboratory skills and exercises illustrate key concepts from the main textbook. • BUILT-IN PEDAGOGY: Pre-lab questions prepare students for each lab and end-of-experiment questions assess student understanding. • FLEXIBLE AND CONVENIENT. The manual is three-hole punched and features perforated pages, which make it easy for student to hand in lab reports and answers to pre- and post-lab questions and exercises upon instructor request. CONTENTS SAFETY-SCALE LABORATORY EXPERIMENTS FOR CHEMISTRY FOR TODAY,

8E Spencer L. Seager, Weber State University; Michael R Slabaugh, Weber State University This proven lab manual offers a unique blend of laboratory skills and exercises that effectively illustrate concepts from the main text, CHEMISTRY FOR TODAY: GENERAL, ORGANIC, AND BIOCHEMISTRY, 8e. The book’s 15 general chemistry and 20 organic/biochemistry safetyscale laboratory experiments use small quantities of chemicals and emphasize safety and proper disposal of materials. “Safety-scale’ is the authors’ own term for describing the amount of chemicals each lab experiment requires--less than macroscale quantities, which are expensive and hazardous, and more than microscale quantities, which are difficult to work with and require special equipment. 1. Matter, Measurements, and Calculations2 Atoms and Molecules.3 Electronic Structure and the Periodic Law.4 Forces Between Particles5 Chemical Reactions.6 The States of Matter7 Solutions and Colloids.8 Reaction Rates and Equilibrium9 Acids,

Bases, and Salts.10 Radioactivity and Nuclear Processes.11 Organic Compounds: Alkanes.12 Unsaturated Hydrocarbons13 Alcohols, Phenols, and Ethers.14 Aldehydes and Ketones.15 Carboxylic Acids and Esters16 Amines and Amides.17 Carbohydrates18 Lipids.19 Proteins20 Enzymes21 Nucleic Acids and Protein Synthesis.22 Nutrition and Energy for Life.23 Carbohydrate Metabolism24 Lipid and Amino Acid Metabolism.25 Body FluidsAppendix A: The International System of Measurements. Appendix B: Answers to Even-Numbered Endof-Chapter Exercises.Appendix C: Solutions to Learning Checks.GlossaryIndex 2014, 544pp, Paperback, 9781133604259 www.cengageasiacom 19 Source: http://www.doksinet are identified with an icon. • Up to date coverage throughout the text, but especially the biochemistry chapters. Biochemistry is an ever changing field and the new edition has been updated with the latest information in that field. • OWL and Youbook: OWL now includes more parameterized end-of-chapter questions,

encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. Also includes Student Self Assessments, the interactive customizable Cengage YouBook, and an optional Solutions Manual eBook. GENERAL, ORGANIC, AND BIOLOGICAL CHEMISTRY, INTERNATIONAL EDITION, 6E FEATURES H. Stephen Stoker, Weber State University Emphasizing the applications of chemistry and minimizing complicated mathematics, GENERAL, ORGANIC, AND BIOLOGICAL CHEMISTRY, 6E, International Edition is written throughout to help students succeed in the course and master the biochemistry content so important to their future careers. The Sixth Edition’s clear explanations, visual support, and effective pedagogy combine to make the text ideal for allied health majors. Early chapters focus on fundamental chemical principles while later chapters build on the foundations of these principles. Mathematics is

introduced at pointof-use and only as needed NEW TO THIS EDITION • Several new ChemistryAt-A-Glance boxes covering critical chemistry concepts have been added to this edition. • New Chemical Connection Boxes covering a variety of topics that relate chemistry to our everyday lives!. • Heavily revised art and photography program. Talking labels have been added to many of the illustrationsthese labels help students understand the concepts being discussed in the figure. • New questions and problems have been added to the end of chapter question/problem sets including a new type of problem that is related to the Chemical Connection boxesthe new questions 20 • Chemistry at-a-Glance features provide brief visual summaries of core chapter concepts to help students visualize difficult material. • Chemical Connection Boxes show chemistry as it relates to everyday life, highlighting its relevance to students’ future careers in the health and environmental fields. • Chemical

Connection Boxes show chemistry as it relates to everyday life, highlighting its relevance to students’ future careers in the health and environmental fields. • Chemical Connection Boxes show chemistry as it relates to everyday life, highlighting its relevance to students’ future careers in the health and environmental fields. CONTENTS PART I: GENERAL CHEMISTRY.1 Basic Concepts About Matter. Chemistry: The Study of Matter Physical States of Matter. Properties of Matter Changes in Matter. CHEMISTRY AT A GLANCE: Use of the Terms Physical and Chemical. Pure Substances and Mixtures. Elements and Compounds. CHEMISTRY AT A GLANCE: Classes of Matter. Discovery and Abundance of the Elements. Names and Chemical Symbols of the Elements. Atoms and Molecules Chemical Formulas. CHEMICAL CONNECTIONS: “Good” Versus “Bad” Properties for a Chemical Substance Elemental Composition of the Human Body. 2 Measurements in Chemistry. Measurement www.cengageasiacom Source: http://www.doksinet

Systems. Metric System Units Exact and Inexact Numbers. Uncertainty in Measurement and Significant Figures. CHEMISTRY AT A GLANCE: Significant Figures. Significant Figures and Mathematical Operations. Scientific Notation Conversion Factors. Dimensional Analysis CHEMISTRY AT A GLANCE: Conversion Factors. Density. Temperature Scales Heat Energy and Specific Heat. CHEMICAL CONNECTIONS: Body Density and Percent Body Fat; Normal Human Body Temperature. 3 Atomic Structure and the Periodic Table. Internal Structure of an Atom Atomic Number and Mass Number. Isotopes and Atomic Masses CHEMISTRY AT A GLANCE: Atomic Structure. The Periodic Law and the Periodic Table. Metals and Nonmetals. Electron Arrangements Within Atoms CHEMISTRY AT A GLANCE: Shell–Subshell– Orbital Interrelationships. Electron Configurations and Orbital Diagrams. The Electronic Basis for the Periodic Law and the Periodic Table. Classification of the Elements. CHEMISTRY AT A GLANCE: Element Classification Schemes and the

Periodic Table. CHEMICAL CONNECTIONS: Protium, Deuterium, and Tritium: The Three Isotopes of Hydrogen; Metallic Elements and the Human Body; Iron: The Most Abundant Transition Element in the Human Body. 4 Chemical Bonding: The Ionic Bond Model. Chemical Bonds Valence Electrons and Lewis Symbols. The Octet Rule The Ionic Bond Model. The Sign and Magnitude of Ionic Charge Lewis Structures for Ionic Compounds. Chemical Formulas for Ionic Compounds. The Structure of Ionic Compounds. Recognizing and Naming Binary Ionic Compounds. CHEMISTRY AT A GLANCE: Ionic Bonds and Ionic Compounds. Polyatomic Ions Chemical Formulas and Names for Ionic Compounds Containing Polyatomic Ions. CHEMISTRY AT A GLANCE: Nomenclature of Ionic Compounds. CHEMICAL CONNECTIONS: Fresh Water, Seawater, Hard Water, and Soft Water: A Matter of Ions; Tooth Enamel: A Combination of Monatomic and Polyatomic Ions. 5 Chemical Bonding: The Covalent Bond Model. The Covalent Bond Model Lewis Structures for Molecular Compounds.

Single, Double, and Triple Covalent Bonds. Valence Electrons and Number of Covalent Bonds Formed. Coordinate Covalent Bonds. Systematic Procedures for Drawing Lewis Structures. Bonding in Compounds with Polyatomic Ions Present. Molecular Geometry CHEMISTRY AT A GLANCE: The Geometry of Molecules. Electronegativity Bond Polarity Molecular Polarity. CHEMISTRY AT A GLANCE: Covalent Bonds and Molecular Compounds. Naming Binary Molecular Compounds. CHEMICAL CONNECTIONS: Nitric Oxide: A Molecule Whose Bonding Does Not Follow “The Rules”; The Chemical Senses of Smell and Taste. 6 Chemical Calculations: Formula Masses, Moles, and Chemical Equations. Formula Masses The Mole: A Counting Unit for Chemists. The Mass of a Mole Chemical Formulas and the Mole Concept. The Mole and Chemical Calculations. Writing and Balancing Chemical Equations. Chemical Equations and the Mole Concept. CHEMISTRY AT A GLANCE: Relationships Involving the Mole Concept. Chemical Calculations Using Chemical Equations.

CHEMICAL CONNECTIONS: Carbon Monoxide Air Pollution: A Case of Combining Ratios Chemical Reactions on an Industrial Scale: Sulfuric Acid. 7 Gases, Liquids, and Solids. The Kinetic Molecular Theory of Matter Kinetic Molecular Theory and Physical States. Gas Law Variables. Boyle’s Law: A Pressure-Volume Relationship. Charles’s Law: A TemperatureVolume Relationship The Combined Gas Law The Ideal Gas Law. Dalton’s Law of Partial Pressures CHEMISTRY AT A GLANCE: The Gas Laws. Changes of State. Evaporation of Liquids Vapor Pressure of Liquids. Boiling and Boiling Point Intermolecular Forces in Liquids. CHEMISTRY AT A GLANCE: Intermolecular Forces. CHEMICAL CONNECTIONS: The Importance of Gas Densities; Blood Pressure and the Sodium Ion/Potassium Ion Ratio; Hydrogen Bonding and the Density of Water. 8. Solutions Characteristics of Solutions Solubility Solution Formation. Solubility Rules Solution Concentration Units. Dilution CHEMISTRY AT A GLANCE: Solutions. Colloidal Dispersions and

Suspensions. Colligative Properties of Solutions Osmosis and Osmotic Pressure. CHEMISTRY AT A GLANCE: Summary of Colligative Property Terminology. Dialysis CHEMICAL CONNECTIONS: Factors Affecting Gas Solubility; Solubility of Vitamins; Controlled-Release Drugs: Regulating Concentration, Rate, and Location of Release; The www.cengageasiacom 21 Source: http://www.doksinet Artificial Kidney: A Hemodialysis Machine. 9 Chemical Reactions. Types of Chemical Reactions Redox and Nonredox Chemical Reactions. CHEMISTRY AT A GLANCE: Types of Chemical Reactions. Terminology Associated with Redox Processes. Collision Theory and Chemical Reactions. Exothermic and Endothermic Chemical Reactions. Factors That Influence Chemical Reaction Rates. Chemical Equilibrium CHEMISTRY AT A GLANCE: Factors That Increase Reaction Rates. Equilibrium Constants Altering Equilibrium Conditions: Le Châtelier’s Principle. CHEMICAL CONNECTIONS: Combustion Reactions, Carbon Dioxide, and Global Warming;

“Undesirable” Oxidation–Reduction Processes: Metallic Corrosion; Stratospheric Ozone: An Equilibrium Situation. 10 Acids, Bases, and Salts. Arrhenius Acid–Base Theory. Brønsted–Lowry Acid–Base Theory Mono, Di-, and Triprotic Acids CHEMISTRY AT A GLANCE: Acid–Base Definitions. Strengths of Acids and Bases. Ionization Constants for Acids and Bases. Salts Acid–Base Neutralization Chemical Reactions. Self-Ionization of Water The pH Concept. The pKa Method for Expressing Acid Strength. The pH of Aqueous Salt Solutions CHEMISTRY AT A GLANCE: Acids and Acidic Solutions. Buffers The Henderson–Hasselbalch Equation. CHEMISTRY AT A GLANCE: Buffer Systems. Electrolytes Equivalents and Milliequivalents of Electrolytes. Acid–Base Titrations CHEMICAL CONNECTIONS: Excessive Acidity Within the Stomach: Antacids and Acid Inhibitors; Acid Rain: Excess Acidity; Blood Plasma pH and Hydrolysis; Buffering Action in Human Blood; Electrolytes and Body Fluids. 11 Nuclear Chemistry Stable

and Unstable Nuclides. The Nature of Radioactive Emissions. Equations for Radioactive Decay. Rate of Radioactive Decay CHEMISTRY AT A GLANCE: Radioactive Decay. Transmutation and Bombardment Reactions. Radioactive Decay Series. Chemical Effects of Radiation Biochemical Effects of Radiation. Detection of Radiation Sources of Radiation Exposure. Nuclear Medicine Nuclear Fission and Nuclear Fusion. CHEMISTRY AT A GLANCE: Characteristics of Nuclear Reactions. Nuclear and Chemical Reactions Compared. CHEMICAL CONNECTIONS: Tobacco Radioactivity 22 and the Uranium-238 Decay Series; Preserving Food Through Food Irradiation; The Indoor Radon-222 Problem.PART II: ORGANIC CHEMISTRY.12 Saturated Hydrocarbons Organic and Inorganic Compounds. Bonding Characteristics of the Carbon Atom. Hydrocarbons and Hydrocarbon Derivatives. Alkanes: Acyclic Saturated Hydrocarbons. Structural Formulas Alkane Isomerism. Conformations of Alkanes IUPAC Nomenclature for Alkanes. Line-Angle Structural Formulas for

Alkanes. CHEMISTRY AT A GLANCE: Structural Representations for Alkane Molecules. Classification of Carbon Atoms. Branched-Chain Alkyl Groups. Cycloalkanes IUPAC Nomenclature for Cycloalkanes. Isomerism in Cycloalkanes Sources of Alkanes and Cycloalkanes. Physical Properties of Alkanes and Cycloalkanes. Chemical Properties of Alkanes and Cycloalkanes. CHEMISTRY AT A GLANCE: Properties of Alkanes and Cycloalkanes. Nomenclature and Properties of Halogenated Alkanes. CHEMICAL CONNECTIONS: The Occurrence of Methane; The Physiological Effects of Alkanes; Chlorofluorocarbons and the Ozone Layer. 13 Unsaturated Hydrocarbons Unsaturated Hydrocarbons. Characteristics of Alkenes and Cycloalkenes. IUPAC Nomenclature for Alkenes and Cycloalkenes. Line-Angle Structural Formulas for Alkenes. Constitutional Isomerism in Alkenes. Cis–Trans Isomerism in Alkenes Naturally Occurring Alkenes. Physical Properties of Alkenes and Cycloalkenes. Chemical Reactions of Alkenes Polymerization of Alkenes:

Addition Polymers. Alkynes. CHEMISTRY AT A GLANCE: Chemical Reactions of Alkenes 383. CHEMISTRY AT A GLANCE: IUPAC Nomenclature for Alkanes, Alkenes, and Alkynes. Aromatic Hydrocarbons Names for Aromatic Hydrocarbons. Aromatic Hydrocarbons: Physical Properties and Sources. Chemical Reactions of Aromatic Hydrocarbons. Fused-Ring Aromatic Hydrocarbons. CHEMICAL CONNECTIONS: Ethene: A Plant Hormone and High-Volume Industrial Chemical; Cis–Trans Isomerism and Vision; Carotenoids: A Source of Color; Fused-Ring Aromatic Hydrocarbons and Cancer. 14 Alcohols, Phenols, and Ethers Bonding Characteristics of Oxygen Atoms in Organic Compounds. Structural Characteristics of Alcohols www.cengageasiacom Source: http://www.doksinet Nomenclature for Alcohols. Isomerism for Alcohols Important Commonly Encountered Alcohols. Physical Properties of Alcohols. Preparation of Alcohols. Classification of Alcohols Chemical Reactions of Alcohols. CHEMISTRY AT A GLANCE: Summary of Chemical Reactions

Involving Alcohols. Polymeric Alcohols. Structural Characteristics of Phenols. Nomenclature for Phenols Physical and Chemical Properties of Phenols. Occurrence of and Uses for Phenols. Structural Characteristics of Ethers. Nomenclature for Ethers Isomerism for Ethers. Physical and Chemical Properties of Ethers Cyclic Ethers. Sulfur Analogs of Alcohols Sulfur Analogs of Ethers. CHEMICAL CONNECTIONS: Menthol: A Useful Naturally Occurring Terpene Alcohol; Ethers as General Anesthetics; Marijuana: The Most Commonly Used Illicit Drug; Garlic and Onions: Odiferous Medicinal Plants. CHEMISTRY AT A GLANCE: Alcohols, Thiols, Ethers, and Thioethers. 15 Aldehydes and Ketones The Carbonyl Group. Compounds Containing a Carbonyl Group. The Aldehyde and Ketone Functional Groups. Nomenclature for Aldehydes Nomenclature for Ketones. Isomerism for Aldehydes and Ketones Selected Common Aldehydes and Ketones. Physical Properties of Aldehydes and Ketones. Preparation of Aldehydes and Ketones. Oxidation and

Reduction of Aldehydes and Ketones. Reaction of Aldehydes and Ketones with Alcohols. CHEMISTRY AT A GLANCE: Summary of Chemical Reactions Involving Aldehydes and Ketones. Formaldehyde-Based Polymers. Sulfur-Containing Carbonyl Groups. CHEMICAL CONNECTIONS: Lachrymatory Aldehydes and Ketones; Melanin: A Hair and Skin Pigment; Diabetes, Aldehyde Oxidation, and Glucose Testing.16 Carboxylic Acids, Esters, and Other Acid Derivatives. Structure of Carboxylic Acids and Their Derivatives. IUPAC Nomenclature for Carboxylic Acids. Common Names for Carboxylic Acids. Polyfunctional Carboxylic Acids. Metabolic Acids Physical Properties of Carboxylic Acids. Preparation of Carboxylic Acids. Acidity of Carboxylic Acids Carboxylic Acid Salts. Structure of Esters Preparation of Esters. CHEMISTRY AT A GLANCE: Summary of the “H Versus R” Relationship for Pairs of Hydrocarbon Derivatives. Nomenclature for Esters. Selected Common Esters Isomerism for Carboxylic Acids and Esters. Physical Properties of

Esters. Chemical Reactions of Esters Sulfur Analogs of Esters. CHEMISTRY AT A GLANCE: Summary of Chemical Reactions Involving Carboxylic Acids and Esters. Polyesters Acid Chlorides and Acid Anhydrides. Esters and Anhydrides of Inorganic Acids. CHEMICAL CONNECTIONS: Nonprescription Pain Relievers Derived from Propanoic Acid Carboxylic Acids and Skin Care; Aspirin; Nitroglycerin: An Inorganic Triester. 17 Amines and Amides Bonding Characteristics of Nitrogen Atoms in Organic Compounds. Structure and Classification of Amines Nomenclature for Amines. Isomerism for Amines Physical Properties of Amines. Basicity of Amines Amine Salts. Preparation of Amines and Quaternary Ammonium Salts. Heterocyclic Amines Selected Biochemically Important Amines. Alkaloids Structure and Classification of Amides. Nomenclature for Amides. Selected Amides and Their Uses Physical Properties of Amides. Preparation of Amides. Hydrolysis of AmidesPolyamides and Polyurethanes. CHEMISTRY AT A GLANCE: Summary of

Chemical Reactions Involving Amines and Amides. CHEMICAL CONNECTIONS: Caffeine: The Most Widely Used Central Nervous System Stimulant; Nicotine Addiction: A Widespread Example of Drug Dependence; Alkaloids Present in Chocolate; Acetaminophen: A Substituted Amide. PART III: BIOLOGICAL CHEMISTRY.18 Carbohydrates. BiochemistryAn Overview Occurrence and Functions of Carbohydrates. Classification of Carbohydrates. Chirality: Handedness in Molecules. Stereoisomerism: Enantiomers and Diastereomers. Designating Handedness Using Fischer Projection Formulas. CHEMISTRY AT A GLANCE: Constitutional Isomers and Stereoisomers. Properties of Enantiomers Classification of Monosaccharides. Biochemically Important Monosaccharides. Cyclic Forms of Monosaccharides. Haworth Projection Formulas Reactions of Monosaccharides. Disaccharides CHEMISTRY AT A GLANCE: “Sugar Terminology” Associated with Monosaccharides and Their Derivatives. General Characteristics of Polysaccharides. Storage Polysaccharides

www.cengageasiacom 23 Source: http://www.doksinet Structural Polysaccharides. CHEMISTRY AT A GLANCE: Types of Glycosidic Linkages for Common Glucose-Containing Diand Polysaccharides. Acidic Polysaccharides. Glycolipids and Glycoproteins: Cell Recognition. Dietary Considerations and Carbohydrates. CHEMICAL CONNECTIONS: Blood Types and Monosaccharides; Lactose Intolerance and Galactosemia; Changing Sugar Patterns: Decreased Sucrose, Increased Fructose; Artificial Sweeteners; “Good and Bad Carbs”: The Glycemic Index. 19 Lipids Structure and Classification of Lipids. Types of Fatty Acids Physical Properties of Fatty Acids. Energy-Storage Lipids: Triacylglycerols Dietary Considerations and Triacylglycerols. Chemical Reactions of Triacylglycerols. CHEMISTRY AT A GLANCE: Classification Schemes for Fatty Acid Residues Present in Triacylglycerols. Membrane Lipids: Phospholipids. Membrane Lipids: Sphingoglycolipids. CHEMISTRY AT A GLANCE: Terminology for and Structural Relationships

Among Various Types of Fatty-Acid-Containing Lipids. Membrane Lipids: Cholesterol. Cell Membranes Emulsification Lipids: Bile Acids. Messenger Lipids: Steroid Hormones. Messenger Lipids: Eicosanoids Protective-Coating Lipids: Biological Waxes. CHEMISTRY AT A GLANCE: Types of Lipids in Terms of How They Function. CHEMICAL CONNECTIONS: The Fat Content of Tree Nuts and Peanuts; Artificial Fat Substitutes; The Cleansing Action of Soap; Trans Fatty Acids and Blood Cholesterol Levels; Steroid Drugs in Sports; The Mode of Action for Anti-Inflammatory Drugs. 20 Proteins. Characteristics of Proteins Amino Acids: The Building Blocks for Proteins. Chirality and Amino Acids. Acid–Base Properties of Amino Acids Cysteine: A Chemically Unique Amino Acid. Peptides. Biochemically Important Small Peptides General Structural Characteristics of Proteins. Primary Structure of Proteins. Secondary Structure of Proteins. Tertiary Structure of Proteins Quaternary Structure of Proteins. Protein Classification

Based on Shape. Protein Classification Based on Function CHEMISTRY AT A GLANCE: Protein Structure. Protein Hydrolysis. Protein Denaturation Glycoproteins. Lipoproteins CHEMICAL CONNECTIONS: The Essential Amino Acids; Substitutes for Human Insulin Protein Structure and 24 the Color of Meat; Denaturation and Human Hair; Cyclosporine: An Antirejection Drug; Lipoproteins and Heart Disease Risk. 21 Enzymes and Vitamins General Characteristics of Enzymes. Enzyme Structure. Nomenclature and Classifi cation of Enzymes. Models of Enzyme Action Enzyme Specificity. Factors That Affect Enzyme Activity CHEMISTRY AT A GLANCE: Enzyme Activity. Enzyme Inhibition. CHEMISTRY AT A GLANCE: Enzyme Inhibition. Regulation of Enzyme Activity Antibiotics That Inhibit Enzyme Activity. Medical Uses of Enzymes. General Characteristics of Vitamins. Water-Soluble Vitamins Fat-Soluble Vitamins. CHEMICAL CONNECTIONS: H pylori and Stomach Ulcers; Enzymatic Browning: Discoloration of Fruits and Vegetables; Heart

Attacks and Enzyme Analysis. 22 Nucleic Acids Types of Nucleic Acids. Nucleotides: Building Blocks of Nucleic Acids. Primary Nucleic Acid Structure CHEMISTRY AT A GLANCE: Nucleic Acid Structure. The DNA Double Helix Replication of DNA Molecules. Overview of Protein Synthesis Ribonucleic Acids. CHEMISTRY AT A GLANCE: DNA Replication. Transcription: RNA Synthesis The Genetic Code. Anticodons and tRNA Molecules Translation: Protein Synthesis. Mutations Nucleic Acids and Viruses. CHEMISTRY AT A GLANCE: Protein Synthesis: Transcription and Translation. Recombinant DNA and Genetic Engineering. The Polymerase Chain Reaction. DNA Sequencing CHEMICAL CONNECTIONS: Use of Synthetic Nucleic Acid Bases in Medicine; Antibiotics That Inhibit Bacterial Protein Synthesis. 23 Biochemical Energy Production. Metabolism Metabolism and Cell Structure. Important Intermediate Compounds in Metabolic Pathways. High-Energy Phosphate Compounds. An Overview of Biochemical Energy Production. The Citric Acid Cycle

CHEMISTRY AT A GLANCE: Simplified Summary of the Four Stages of Biochemical Energy Production. CHEMISTRY AT A GLANCE: Summary of the Reactions of the Citric Acid Cycle. The Electron Transport Chain CHEMISTRY AT A GLANCE: Summary of the Flow of Electrons Through the Four Complexes of the Electron Transport Chain. Oxidative Phosphorylation CHEMISTRY AT A GLANCE: Summary of the Common Metabolic Pathway. ATP Production for www.cengageasiacom Source: http://www.doksinet the Common Metabolic Pathway. The Importance of ATP. Non-ETC Oxygen-Consuming Reactions CHEMICAL CONNECTIONS: Cyanide Poisoning; Brown Fat, Newborn Babies, and Hibernating Animals; Flavonoids: An Important Class of Dietary Antioxidants. 24 Carbohydrate Metabolism Digestion and Absorption of Carbohydrates. Glycolysis. Fates of Pyruvate ATP Production for the Complete Oxidation of Glucose. Glycogen Synthesis and Degradation. Gluconeogenesis Terminology for Glucose Metabolic Pathways. The Pentose Phosphate Pathway.

CHEMISTRY AT A GLANCE: Glucose Metabolism. Hormonal Control of Carbohydrate Metabolism. CHEMICAL CONNECTIONS: Lactate Accumulation; Diabetes Mellitus. 25 Lipid Metabolism Digestion and Absorption of Lipids. Triacylglycerol Storage and Mobilization. Glycerol Metabolism Oxidation of Fatty Acids. ATP Production from Fatty Acid Oxidation. Ketone Bodies Biosynthesis of Fatty Acids: Lipogenesis. Relationships Between Lipogenesis and Citric Acid Cycle Intermediates. Biosynthesis of Cholesterol. CHEMISTRY AT A GLANCE: Interrelationships Between Carbohydrate and Lipid Metabolism. Relationships Between Lipid and Carbohydrate Metabolism. CHEMICAL CONNECTIONS: High-Intensity Versus LowIntensity Workouts; Statins: Drugs That Lower Plasma Levels of Cholesterol. 26 Protein Metabolism. Protein Digestion and Absorption Amino Acid Utilization. Transamination and Oxidative Deamination. The Urea Cycle Amino Acid Carbon Skeletons. Amino Acid Biosynthesis Hemoglobin Catabolism. CHEMISTRY AT A GLANCE:

Interrelationships Among Carbohydrate, Lipid, and Protein Metabolism. Interrelationships Among Metabolic Pathways. CHEMICAL CONNECTIONS: The Chemical Composition of Urine Arginine, Citrulline, and the Chemical Messenger Nitric Oxide. Answers to Selected Exercises A-1. 2013, 1056pp, Paperback, 9781133106869 INTRODUCTION TO GENERAL, ORGANIC AND BIOCHEMISTRY, INTERNATIONAL EDITION, 10E Frederick A. Bettelheim, Adelphi University; William H Brown, Beloit College; Mary K. Campbell, Mount Holyoke College; Shawn O. Farrell, Olympic Training Center This bestselling text continues to lead the way with a strong focus on current issues, pedagogically rich framework, wide variety of medical and biological applications, visually dynamic art program, and exceptionally strong and varied end-of-chapter problems. Revised and updated throughout, the tenth edition now includes new biochemistry content, new Chemical Connections essays, new and revised problems, and more. Every problem from the tenth

edition is now available in the OWL online learning system. NEW TO THIS EDITION • Ten percent of the book’s problems are new or revised. In addition, all problems in the tenth edition are now available in the OWL online learning system. • New “Chemical Connections” boxes such as, “DDT, A Boon and a Curse,” “From Moldy Clover to a Blood Thinner,” and “Is There a Connection Between Carbohydrates and Obesity?” have been added to the text’s more than 150 Chemical Connections essays. End-of-chapter problems associated with “Chemical Connections” are now keyed to provide students with immediate reinforcement. • New up-to-date biochemistry coverage includes material on Membrane Cholesterol Function (Chapter 21), Transition Metals and Their Effect on the Structure of Proteins (Chapter 22), Enzyme www.cengageasiacom 25 Source: http://www.doksinet • • • • • • Inhibitors in Medicine (Chapter 23), Obesity and Type-II Diabetes (Chapter 24),

Synthetic Genome (Chapter 26), Nutrient Deficiencies Linked to Depression (Chapter 30), and Immunization (Chapter 31). Coverage of balancing chemical equations now appears earlier in Chapter 4, Chemical Reactions, and the more difficult calculations involving mass relationships have been moved to the end of the chapter. Allotropes of carbon are now included in an expanded Section 5.9, What Are the Characteristics of the Various Types of Solids? Chapter 8, Acids and Bases, now covers the Activity Series. A new “How To” box in Chapter 11 emphasizes the skills students need to master “How to Draw Alternative Chair Conformations of Cyclohexane.” Organic mechanisms are now simplified into easyto-remember steps: add a proton, take a proton away, break a bond, and make a bond in Chapter 12, Alkenes and Alkynes. An enhanced version of the OWL online learning system now includes Interactive Examples from the text and more parameterized end-of-chapter questions that encourage students to

practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. In addition, OWL now includes a multimedia eBook, the interactive customizable Cengage YouBook, as well as an optional Solutions Manual eBook. CONTENTS 1. Matter, Energy, and Measurement 2 Atoms 3 Chemical Bonds. 4 Chemical Reactions 5 Gases, Liquids, and Solids. 6 Solutions and Colloids 7. Reaction Rates and Chemical Equilibrium 8 Acids and Bases.9 Nuclear Chemistry 10 Organic Chemistry. 11 Alkanes 12 Alkenes and Alkynes 13. Benzene and Its Derivatives 14 Alcohols, Ethers, and Thiols. 15 Chirality: The Handedness of Molecules. 16 Amines 17 Aldehydes and Ketones 18. Carboxylic Acids 19 Carboxylic Anhydrides, Esters, and Amides. 20 Carbohydrates 21 Lipids. 22 Proteins 23 Enzymes 24 Chemical Communications: Neurotransmitters and Hormones. 25. Nucleotides, Nucleic Acids, and Heredity 26 26. Gene Expression and Protein Synthesis 27

Bioenergetics: How the Body Converts Food to Energy. 28 Specific Catabolic Pathways: Carbohydrate, Lipid, and Protein Metabolism. 29. Biosynthetic Pathways 30 Nutrition 31 Immunochemistry.32 Body Fluids(Chapter 32 can be found on this book’s companion website, which is accessible from http://www.cengagecom/ chemistry/bettelheim)Appendix 1. Exponential Notation. Appendix 2 Significant Figures Answers to In-Text and Odd-Numbered End-of-Chapter Problems. GlossaryCreditsIndex 2013, 1008pp, Paperback, 9781133109112 LABORATORY EXPERIMENTS FOR INTRODUCTION TO GENERAL, ORGANIC AND BIOCHEMISTRY, INTERNATIONAL EDITION, 8E Frederick A. Bettelheim, Adelphi University; Joseph M Landesberg, Adelphi University The 48 experiments in this well-conceived manual illustrate important concepts and principles in general, organic, and biochemistry. As in previous editions, three basic goals guided the development of all the experiments: (1) the experiments illustrate the concepts learned in the

classroom; (2) the experiments are clearly and concisely written so that students will easily understand the task at hand, will work with minimal supervision because the manual provides enough information on experimental procedures, and will be able to perform the experiments in a 2-1/2 hour laboratory period; and (3) the experiments are not only simple demonstrations, but also contain a sense www.cengageasiacom Source: http://www.doksinet of discovery. This edition includes many revised experiments and two new experiments. NEW TO THIS EDITION • Many of the experiments have been updated. • Two new experiments Beer’s Law and Standard Curves, and Tyrosinase Enzyme Kinetics have been added. • Many of the pre- and post-lab questions have been revised. FEATURES • The 48 experiments in this manual illustrate important concepts and principles in general, organic, and biochemistry. • The experiments illustrate the concepts learned in the classroom, and are clearly and concisely

written. • The experiments are not only simple demonstrations, but also contain a sense of discovery. CONTENTS Experiment 1: Laboratory Techniques: Using the Laboratory Gas Burner; Making LaboratoryMeasurementsExperiment 2: Density DeterminationExperiment 3: Separation of the Components of a MixtureExperiment 4: Resolution of a Mixture by DistillationExperimnet 5: The Empirical Formula of a Compound: The Law of Constant CompositionExperiment 6: Determination of the Formula of a Metal OxideExperiment 7: Classes of Chemical ReactionsExperiment 8: Chemical Properties of Consumer ProductsExperiment 9: Calorimetry: The Determination of the Specific Heat of a MetalExperimment 10: Boyle’s Law: The Pressure–Volume Relationship of a GasExperiment 11: Charles’s Law: The Volume– Temperature Relationship of a GasExperiment 12: Properties of Gases: Determination of the Molar Mass of a Volatile LiquidExperiment 13: Physical Properties of Chemicals: Melting Point, Sublimation, and Boiling

PointExperiment 14: Solubility and SolutionsExperiment 15: Water of HydrationExperiment 16: Factors Affecting Reaction RatesExperiment 17: The Law of Chemical Equilibrium and Le Chatelier’s PrincipleExperiment 18: pH and Buffer SolutionsExperiment 19: Analysis of Vinegar by TitrationExperiment 20: Analysis of Antacid TabletsExperiment 21: Structure in Organic Compounds: Use of Molecular Models. IExperiment 22: Stereochemistry: Use of Molecular Models. IIExperiment 23: Column and Paper Chromatography: Separation of Plant PigmentsExperiment 24: Classification and Identification of HydrocarbonsExperiment 25: Classification and Identification of Alcohols and PhenolsExperiment 26: Classification and Identification of Aldehydes and KetonesExperiment 27: Properties of Carboxylic Acids and EstersExperiment 28: Properties of Amines and AmidesExperiment 29: Polymerization ReactionsExperiment 30: Preparation of Acetylsalicylic Acid (Aspirin) Experiment 31: Isolation of Caffeine from Tea

LeavesExperiment 32: CarbohydratesExperiment 33: Fermentation of a Carbohydrate:Ethanol from SucroseExperiment 34: Preparation and Properties of a SoapExperiment 35: Preparation of a Hand CreamExperiment 36: Extraction and Identification of Fatty Acids from Corn OilExperiment 37: Analysis of LipidsExperimnet 38: Separation of Amino Acids by Paper ChromatographyExperiment 39: Acid– Base Properties of Amino AcidsExperiment 40: Isolation and Identification of CaseinExperiment 41: Properties of EnzymesExperiment 42: Neurotransmission: An Example of Enzyme SpecificityExperiment 43: Isolation and Identification of DNA from OnionExperiment 44: Viscosity and Secondary Structure of DNAExperiment 45: Beer’s Law and Standard CurvesExperiment 46: Tyrosinase Enzyme KineticsExperiment 47: Quantitative Analysis of Vitamin C Contained in FoodsExperiment 48: Analysis of Vitamin A in Margarine 2013, 656pp, Paperback, 9781133113102 www.cengageasiacom 27 Source: http://www.doksinet Acid-Base

Properties of Amino Acids.13 Isolation and Identification of Casein.14 Enzymes 2012, 256pp, Paperback, 9781111426613 BASIC LABORATORY EXPERIMENTS FOR GENERAL, ORGANIC, AND BIOCHEMISTRY Joseph M. Landesberg, Adelphi University Succeed in your GOB Lab course with the easyto-follow experiments in this streamlined and focused manual. Fourteen experiments (6 general chemistry, 4 organic chemistry, and 4 biochemistry) illustrate the concepts you must know for your future allied health career, while pre- and post-lab questions test your ability to apply concepts. FEATURES • DESIGNED FOR NURSING AND HEALTH SCIENCE MAJORS. Focusing on the key concepts most important to allied health majors, this streamlined lab manual is ideal for the one-term General, Organic, and Biochemistry laboratory course. • CLEAR AND STRAIGHTFORWARD. Clear directions help students complete labs successfully. • A FOCUS ON APPLICATION. Pre- and post-lab questions for every experiment test the student’s ability

to understand and apply concepts. CONTENTS 1. Laboratory Measurements2 Density Determination.3 Classes of Chemical Reactions4 Separation of Components of a Mixture.5 Factors Affecting Rate of Reactions.6 The Law of Chemical Equilibrium and the Le Chatelier Principle.7 pH and Buffer Solutions.8 Structure and Stereochemistry in Organic Compounds, the Use of Molecular Models.9 Aspirin: Preparation and Properties (Acetylsalicylic Acid).10 Carbohydrates11 Fats and Oils: Preparation and Properties of Soap.12 28 GENERAL, ORGANIC, AND BIOCHEMISTRY An Applied Approach, International Edition James Armstrong, City College of San Francisco Focusing on the needs of allied health and nursing majors, this engaging book is ideal for students who have had no prior exposure to chemistry. The author takes the time to explain how to do tasks that students find difficult, rather than just providing terse descriptions. Emphasizing problem-solving techniques without skipping steps and using terms

students can grasp, the book takes the most direct path to biomolecules and metabolic processes, provides a wealth of worked examples to help students understand key chemical concepts, includes novel and relevant “Health Notes” in the margins, and weaves biological and medical applications throughout. FEATURES • DESIGNED FOR NURSING AND HEALTH SCIENCES MAJORS. This allied health-focused book takes the most direct path to biomolecules and metabolic processes, includes novel and relevant “Health Notes” in the margins, and weaves biological and medical applications throughout to prepare students for their future careers. • EMPHASIS ON PROBLEM SOLVING STRATEGIES. Each Sample Problem is paired with a closely related “Try It Yourself” question. www.cengageasiacom Source: http://www.doksinet • • • • Most sample problems list additional Core Problems that students can do to practice new skills. Steps for solving the conversion problems appear in the margins to

guide students through the problem-solving process. FOCUSED ON STUDENT LEARNING. Each chapter begins with a short health-related, ‘story type’ introduction, followed by numbered sections with learning objectives. Sectionending Core Problems immediately reinforce the section objectives and help students’ gauge their knowledge of the content. Key Terms appear in boldface type the first time they are used and are collected at the back of the chapter to facilitate student review. BUILT-IN STUDY GUIDE. End-of-chapter material (keyed to each section) helps students master chapter concepts and problem-solving skills and review for quizzes and tests. Concept Questions encourage students to describe how the ideas in the chapter apply to specific examples, while Summary and Challenge Problems cover all sections and give instructors the opportunity to assign questions at a wide range of levels. Challenge problems are marked with an asterisk and require a greater depth of understanding; many

involve concepts from earlier chapters. OWL INTEGRATION. Improve student learning outcomes with OWL, the #1 online homework and learning system for chemistry. Developed by chemistry instructors for teaching chemistry, OWL includes course management tools that make homework management a breeze, as well as advanced reporting and grade book features that save time in grading homework and tracking student progress. OWL enables you to address students’ different learning styles through tutorials, simulations, visualization exercises, and algorithmically-generated homework questions with answer-specific feedback. With OWL’s mastery learning approach, students work at their own pace until they understand each concept/ skill. OWL includes an eBook, enhanced with multimedia learning tools. EXPERT REVIEW: The entire text was reviewed by Nursing Professor Kellee Hollyman, RN,BSN, MN-Nurse Educator to ensure the relevance and accuracy of the health material. CONTENTS 1. MEASUREMENTS IN

SCIENCE AND MEDICINE.Measuring Size: Distance, Mass, and Volume. Metric Units and Their Relationships Rounding and Precision In Measurements. Unit Conversions and Conversion Factors. Rounding and Significant Figures. Temperature Density, Dosage, and Other Compound Units.2 ATOMS, ELEMENTS, AND COMPOUNDS.Classifying Matter: Mixtures, Compounds, and Elements. The Chemical Elements: An Introduction to the Periodic Table. Atoms Subatomic Particles and Atomic Structure.Isotopes And Atomic Weight Chemical Formulas. Electron Shells Chemical Behavior, Valence Electrons, and the Periodic Law. The Organization of the Periodic Table3 CHEMICAL BONDS.Covalent Bonds and the Octet Rule. Double And Triple Bonds Drawing Lewis Structures for Complex Molecules. Electronegativity and Polar Bonds. Naming Covalent Compounds Ions and Ionic Compounds. Writing Formulas for Ionic Compounds. Naming Ionic Compounds Polyatomic Ions. Recognizing Ionic and Molecular Compounds.4 ENERGY AND THE PHYSICAL BEHAVIOR OF

CHEMICAL SUBSTANCES.Heat and Energy. The Three States of Matter The Properties of Gases. Changes of State Attractive Forces and the Physical Properties of Matter.5 SOLUTIONS AND CONCENTRATION.Solutions and the Dissolving Process. Electrolytes and Dissociation. Solubility The Relationship Between Solubility and Molecular Structure. Concentration Moles and Formula Weights. Molarity Osmosis, Dialysis, And Tonicity. Equivalents Dilution6 CHEMICAL REACTIONS.Physical Changes and Chemical Reactions. Chemical Equations Mass Relationships in a Chemical Reaction. Heats of Reaction. Combustion and Precipitation Reactions. Reaction Rate and Activation Energy Chemical Equilibrium.7 ACIDS AND BASES The Self-Ionization of Water. The Ph Scale The Properties of Acids. The Properties of Bases AcidBase Reactions Amphiprotic Molecules and Ions Buffers.The Role of Buffers in Human Physiology8 HYDROCARBONS – AN INTRODUCTION TO ORGANIC MOLECULES.The Special Properties of www.cengageasiacom 29 Source:

http://www.doksinet Carbon. Linear Alkanes: The Foundation of Organic Chemistry. Branched Alkanes, Cycloalkanes, and Isomers. Naming Branched Alkanes: The IUPAC System. Functional Groups Alkenes and Alkynes Geometric Isomers. Benzene and Aromatic Compounds. The Properties of Hydrocarbons9 HYDRATION, DEHYDRATION AND ALCOHOLS. The Hydration Reaction. Controlling the Product – An Introduction to Enzymes. Naming Alcohols The Physical Properties of Alcohols. The Dehydration Reaction. Phenols and Thiols10 CARBONYL COMPOUNDS AND REDOX REACTIONS. Hydrogenation and Dehydrogenation. Oxidation and Reductions. Reactions and the Carbonyl Group. The Naming and Properties of Aldehydes and Ketones. Other Oxidation and Reduction Reactions. Carboxylic Acids Biological Oxidations and Reductions – The Redox Coenzymes. Introduction to Metabolic Pathways.11 ORGANIC ACIDS AND BASES.Reactions of Organic Acids Decarboxylation Reactions. Amines The AcidBase Reactions of Amines Amines in Biology and

Medicine. The Relationship Between Structure and Ph.12 BUILDING LARGE MOLECULES – CONDENSATION AND HYDROLYSIS REACTIONS.Introduction to Condensation Reactions – Ethers. Esterification, Amidation, and Phosphorylation. Condensation Polymers Hydrolysis. The Effect of Ph on the Products of Hydrolysis. The Equilibrium Between Condensation and Hydrolysis.13 PROTEINSAmino acids Peptide bonds and the secondary structure of a protein. Side chain interactions and tertiary structure. Protein denaturation. Enzyme structure and function Cofactors. Antibodies and the immune response Sources of amino acids.14: CARBOHYDRATES AND LIPIDS.Monosaccharides Isomeric Forms Of Monosaccharides – Anomers and Enantiomers. Disaccharides and the Glycosidic Linkage. Common Disaccharides and Polysaccharides.Fatty Acids and Triglycerides. The Chemical Reactions of Triglycerides. Glycerophospholipids and Cell Membranes. Steroids and Lipoproteins Sources of Carbohydrates and Fats.15 METABOLISM – THE CHEMICAL

WEB OF LIFE.Catabolism, Anabolism, and the ATP Cycle. An Overview of Catabolism. ATP Production and the Mitochondria 30 Glycolysis. The Citric Acid Cycle Beta Oxidation – Obtaining Energy from Fatty Acids. Catabolism of Amino Acids. Anabolic Pathways and the Control of Metabolism.16 NUCLEIC ACIDS, PROTEIN SYNTHESIS, AND HEREDITY.Nucleotides The Structure of Nucleic Acids. DNA Replication Transcription and RNA Processing. Translation and The Genetic Code. The Mechanism of Protein Synthesis.Regulation of Protein Synthesis Mutations and Genetic Disorders.17 NUCLEAR CHEMISTRY.Symbols for Nuclei And Subatomic Particles. Writing Nuclear Equations Energy and Nuclear Reactions. Physiological Effects of Ionizing Radiation. Measuring Radiation Nuclear Decay and Half-Life. Medical Applications of Nuclear Radiation. Nuclear Fission and FusionAPPENDIX A: ESSENTIAL MATHEMATICS FOR CHEMISTRY. Decimal Notation. Place Value, Fractions, and Division. Order of Operations Exponents Scientific

Notation. Calculator UseAPPENDIX B: THE QUANTITATIVE BEHAVIOR OF GASES.(Kelvin temperature, combined gas law, Avogadro’s law, ideal gas law). 2012, 832pp, Paperback, 9780840068286 www.cengageasiacom Source: http://www.doksinet • • INTRODUCTORY CHEMISTRY FOR TODAY, INTERNATIONAL EDITION, 7E Spencer L. Seager, Weber State University; Michael R Slabaugh, Weber State University • Distinguished by its superior allied health focus and integration of technology, Seager and Slabaugh’s INTRODUCTORY CHEMISTRY FOR TODAY, 7e, International Edition continues to meet students’ needs through diverse applications, examples, boxes, and outstanding technology tools. Prompts throughout the new edition lead students to OWL (web-based learning system)two unique online programs that extend the lessons of the text and help students study smarter. In addition to the many resources found in OWL, the book and website contain questions modeled after the Nursing School and Allied Health

Entrance Exams. INTRODUCTORY CHEMISTRY FOR TODAY, 7e, International Edition dispels students’ inherent fear of chemistry and instills an appreciation for the role chemistry plays in our daily lives through a rich pedagogical structure and an accessible writing style with lucid explanations. In addition, the book provides greater support in both problem-solving and critical-thinking skillsthe skills necessary for student success. By demonstrating the importance of chemistry concepts to students’ future careers and by providing important career information online, the authors not only help students set goals but also help them focus on achieving them. NEW TO THIS EDITION • ALLIED HEALTH CONNECTION. An expanded “Allied-Health Exam Connection” section follows the exercises of each chapter and includes examples of chemistry questions found on typical • entrance examinations used to screen applicants to Allied-Health professional programs. UPDATED ART AND PHOTOGRAPHY PROGRAM.

In addition to adding many new photos to illustrate key concepts, explanations of figures are now incorporated into the art, rather than appearing in the caption, to help students follow processes and understand exactly what is happening within each figure without having to go back and forth between figure and caption. OWL ONLINE LEARNING INTEGRATION. The new edition now contains algorithmically generated versions of most of the end-of-chapters question from the text. NEW AND UPDATED BOXED FEATURES. New “At the Counter” boxes focus on drugs and products found on drugstore shelves and at the pharmacy; “Chemistry Around Us” boxes present everyday applications of chemistry; and updated “Chemistry and Your Health” boxes relate to students’ health and the health of the patients that they may care for in their future roles as a part of the allied health work force. NEW END-OF-CHAPTER EXERCISES. A significant number of the end-of-chapter questions are new. FEATURES • A WEALTH

OF END-OF-CHAPTER EXERCISES. The book’s wide range of end-of-chapter exercises include “Additional Exercises” that are not tied to a specific section and often consist of problems that integrate several concepts and “Chemistry for Thought” exercises that focus on conceptual and cumulative questions and ask students to apply what they have learned to a particular cumulative question. • INTEGRATED LEARNING OBJECTIVES. The book’s Learning Objectives are integrated throughout each chapter and within the summary to help students focus on the chapter’s key skills and concepts. • LEARNING CHECKS. These short, self-check exercises follow the book’s worked-out examples and discussions of key or difficult concepts to help students assess their understanding. • CONCEPT SUMMARY SECTIONS. These endof-chapter sections summarize each chapter’s key www.cengageasiacom 31 Source: http://www.doksinet concepts and include one or two appropriate endof-chapter exercises per

concept. By solving these exercises, students will have an approximate but quick assessment of how well they understand the Learning Objective related to that concept. • HOW REACTIONS OCCUR SECTIONS. These sections present the mechanisms of representative organic reactions to help dispel the mystery of how these reactions take place. CONTENTS 1. Matter, Measurements, and Calculations 2 Atoms and Molecules. 3 Electronic Structure and the Periodic Law. 4 Forces Between Particles 5. Chemical Reactions 6 The States of Matter 7. Solutions and Colloids 8 Reaction Rates and Equilibrium. 9 Acids, Bases, and Salts 10. Radioactivity and Nuclear Processes 11 Organic Compounds: Alkanes. 12 Unsaturated Hydrocarbons. Appendix A: The International System of Measurements. Appendix B: Answers to Even-Numbered End-of-Chapter Exercises. Appendix C: Solutions to Learning Checks. Glossary. Index 2011, 496pp, Paperback, 9780538734868 ORGANIC AND BIOCHEMISTRY FOR TODAY, INTERNATIONAL EDITION, 7E Spencer

L. Seager, Weber State University; Michael R Slabaugh, Weber State University Distinguished by its superior allied health focus and integration of technology, Seager and Slabaugh’s ORGANIC AND BIOCHEMISTRY FOR TODAY, 7e, International Edition continues to meet students’ needs through diverse applications, examples, boxes, and outstanding technology tools and now offers an updated and improved art program. Prompts throughout the new edition lead students to OWL (web-based learning system)two unique online programs that extend the lessons of the text and help students study smarter. In addition to the many resources found in CengageNOW and OWL, the book and website contain questions modeled after the Nursing School and Allied Health Entrance Exams. ORGANIC AND BIOCHEMISTRY FOR TODAY, 7e, International Edition dispels students’ inherent fear of chemistry and instills an appreciation for the role chemistry plays in our daily lives through a rich pedagogical structure and an

accessible writing style with lucid explanations. In addition, the book provides greater support in both problem-solving and critical-thinking skillsthe skills necessary for student success. By demonstrating the importance of chemistry concepts to students’ future careers and by providing important career information online, the authors not only help students set goals but also help them focus on achieving them. NEW TO THIS EDITION • ALLIED HEALTH CONNECTION. An expanded “Allied-Health Exam Connection” section follows 32 www.cengageasiacom Source: http://www.doksinet • • • • the exercises of each chapter and includes examples of chemistry questions found on typical entrance examinations used to screen applicants to Allied-Health professional programs. UPDATED ART AND PHOTOGRAPHY PROGRAM. In addition to adding many new photos to illustrate key concepts, explanations of figures are now incorporated into the art, rather than appearing in the caption, to help

students follow processes and understand exactly what is happening within each figure without having to go back and forth between figure and caption. OWL ONLINE LEARNING INTEGRATION. The new edition now contains algorithmically generated versions of most of the end-of-chapters question from the text. NEW AND UPDATED BOXED FEATURES. New “At the Counter” boxes focus on drugs and products found on drugstore shelves and at the pharmacy; “Chemistry Around Us” boxes present everyday applications of chemistry; and updated “Chemistry and Your Health” boxes relate to students’ health and the health of the patients that they may care for in their future roles as a part of the allied health work force. NEW END-OF-CHAPTER EXERCISES. A significant number of the end-of-chapter questions are new. • CONCEPT SUMMARY SECTIONS. These endof-chapter sections summarize each chapter’s key concepts and include one or two appropriate endof-chapter exercises per concept. By solving these

exercises, students will have an approximate but quick assessment of how well they understand the Learning Objective related to that concept. • HOW REACTIONS OCCUR SECTIONS. These sections present the mechanisms of representative organic reactions to help dispel the mystery of how these reactions take place. CONTENTS 1. Organic Compounds: Alkanes 2 Unsaturated Hydrocarbons. 3 Alcohols, Phenols, and Ethers 4. Aldehydes and Ketones 5 Carboxylic Acids and Esters. 6 Amines and Amides 7 Carbohydrates 8 Lipids. 9 Proteins 10 Enzymes 11 Nucleic Acids and Protein Synthesis. 12 Nutrition and Energy for Life. 13 Carbohydrate Metabolism 14 Lipid and Amino Acid Metabolism. 15 Body Fluids Appendix A: The International System of Measurements. Appendix B: Answers to Even-Numbered Endof-Chapter Exercises. Appendix C: Solutions to Learning Checks. Glossary Index 2011, 512pp, Paperback, 9780538734851 FEATURES • A WEALTH OF END-OF-CHAPTER EXERCISES. The book’s wide range of end-of-chapter

exercises include “Additional Exercises” that are not tied to a specific section and often consist of problems that integrate several concepts and “Chemistry for Thought” exercises that focus on conceptual and cumulative questions and ask students to apply what they have learned to a particular cumulative question. • INTEGRATED LEARNING OBJECTIVES. The book’s Learning Objectives are integrated throughout each chapter and within the summary to help students focus on the chapter’s key skills and concepts. • LEARNING CHECKS. These short, self-check exercises follow the book’s worked-out examples and discussions of key or difficult concepts to help students assess their understanding. www.cengageasiacom 33 Source: http://www.doksinet • FLEXIBLE AND CONVENIENT. The manual is three-hole punched and features perforated pages, which make it easy for student to hand in lab reports and answers to pre- and post-lab questions and exercises upon instructor request. CONTENTS

SAFETY-SCALE LABORATORY EXPERIMENTS FOR CHEMISTRY FOR TODAY, 7E Spencer L. Seager, Weber State University; Michael R Slabaugh, Weber State University Providing a unique blend of laboratory skills and exercises that illustrate concepts from the authors’ main text, CHEMISTRY FOR TODAY: GENERAL, ORGANIC, AND BIOCHEMISTRY, 7e, this accurate and well-tested lab manual contains 15 general chemistry and 20 organic/ biochemistry safety-scale laboratory experiments. The experiments are designed to use small quantities of chemicals and emphasize safety and proper disposal of materials. “Safety-scale” is the authors’ own term for describing the amount of chemicals each lab experiment requires--less than macroscale quantities, which are expensive and hazardous--and more than microscale quantities, which are difficult to work with and require special equipment. NEW TO THIS EDITION • ACCURATE AND CLASS-TESTED. The Seventh Edition includes 15 general chemistry and 20 organic/biochemistry

safety-scale laboratory experiments--all thoroughly class-tested--that effectively illustrate the main text’s key concepts. FEATURES • A KEY CONCEPT FOCUS: The manual’s blend of laboratory skills and exercises illustrate key concepts from the main textbook. • BUILT-IN PEDAGOGY: Pre-lab questions prepare students for each lab and end-of-experiment questions assess student understanding. 34 Introduction.Experiment 1: Measurements and Significant Figures.Experiment 2: The Use of Chemical Balances.Experiment 3: The Use of Volumetric Ware and the Determination of Density. Experiment 4: Physical and Chemical Changes. Experiment 5: Separations and Analysis. Experiment 6: Classification of Chemical Reactions. Experiment 7: Analysis Using Decomposition Reactions.Experiment 8: Gas LawsExperiment 9: Solution Formation and Characteristics. Experiment 10: Colligative Properties of Solutions. Experiment 11: Reactions Rates and Equilibrium. Experiment 12: Acids, Bases, Salts, and Buffers.

Experiment 13: Analysis of Vinegar.Experiment 14: Determination of Ka for Weak Acids.Experiment 15: The Acidic Hydrogens of Acids.Experiment 16: The Use of Melting Points in the Identification of Organic Compounds.Experiment 17: Isolation and Purification of an Organic Compound.Experiment 18: Hydrocarbons.Experiment 19: Reactions of Alcohols and Phenols.Experiment 20: Reactions of Aldehydes and Ketones.Experiment 21: Reactions of Carboxylic Acids, Amines, and Amides.Experiment 22: The Synthesis of Aspirin and Other Esters.Experiment 23: Identifying Functional Groups in Unknowns. Experiment 24: Synthetic Polymers.Experiment 25: Dyes, Inks, and Food Colorings.Experiment 26: A Study of Carbohydrates.Experiment 27: Preparations of Soap by Lipid Saponification. Experiment 28: Isolation of Natural Products: Trimyristin and Cholesterol.Experiment 29: Amino Acids and Proteins.Experiment 30: Enzymes: Nature’s Catalysts.Experiment 31: Factors That Influence Enzyme Activity.Experiment 32:

Vitamin C Content of Foods Part I: Assigned Samples. Experiment 33: Vitamin C Content of Foods Part II: Samples from Home.Experiment 34: Extraction of DNA from Wheat Germ.Experiment 35: Detection www.cengageasiacom Source: http://www.doksinet of Minerals in Breakfast Cereals.APPENDIX A: Graphs and Graphing.APPENDIX B: Equipment, Chemicals, Reagents, and Supplies.APPENDIX C: Table of Atomic Weights and Numbers. 2011, 544pp, Paperback, 9780538734547 • Sample Exercises: Providing step-by-step instruction, Sample Exercises provide detailed explanations to help students gain a solid understanding of GOB concepts and principles. • Avoiding Pitfalls: Included throughout the text, Caution icons alert students to common mistakes and help them understand how to avoid such missteps. • Tips and Tools: Problem Solving Tips give students additional insight for successfully working through exercises. • Flexibility: The modular organization makes this resource an excellent companion for

any GOB textbook. CONTENTS SURVIVAL GUIDE FOR GENERAL, ORGANIC AND BIOCHEMISTRY Richard Morrison, University of Georgia; Charles H. Atwood, University of Georgia; Joel Caughran, University of Georgia Available free in a package with any Cengage Learning chemistry text or available for separate purchase at www.cengagebraincom, this straightforward, thorough SURVIVAL GUIDE FOR GENERAL, ORGANIC AND BIOCHEMISTRY provides everything students need to survive and thrive in the GOB course. Modeled after Atwood’s widely popular GENERAL CHEMISTRY SURVIVAL GUIDE, this guide helps students master concepts, improve essential problem-solving skills, and make the most of their study time, for optimal exam results. Designed as a reader’s guide to a GOB textbook, this extremely reader friendly guide offers detailed step-by-step problem-solving sequences, giving students the competency--and confidence-they need. This brief but powerful resource covers the most fundamental aspects of GOB in a

succinct, straightforward series of essential modules. Module 1: GENERAL CHEMISTRY.1 Metric System, Dimensional Analysis, Significant Figures, Density, and Heat.2 Atomic Theory, Periodicity, Chemical Bonding, and Nomenclature.3 Nuclear Chemistry4 Chemical Reactions and Stoichiometry.5 States of Matter, Solutions, and Colligative Properties.6 Chemical Kinetics.7 Acids and BasesModule 2: ORGANIC CHEMISTRY.8 Functional Groups and Nomenclature.9 Stereoisomerism10 Substitution Reactions.11 Addition Reactions12 Elimination Reactions.13 Oxidation-Reduction Reactions Module 3: BIOCHEMISTRY.14 Carbohydrates15 Lipids.16 Proteins, Protein Synthesis and Enzymes.17 Nucleotides and Gene Expression 2008, 350pp, Paperback, 9780495554691 NEW TO THIS EDITION • Student-Friendly Content: Key Terms, Concepts, and Equations highlight key GOB issues for students, helping them focus on essential concepts and maximize their study time. www.cengageasiacom 35 Source: http://www.doksinet of worked

examples. The Spreadsheet examples, formerly in the Skoog book were off-loaded to the new Excel book so that the burden for teaching about Excel is now on the Excel book. • Precipitation titrations were included in Chapter 9. • Descriptions and instructions written so that they can be used with either the Office 2007 or 2010 versions of Excel. • Cross references to Skoog Fundamentals of Analytical Chemistry, 9e and Skoog, Analytical Chemistry: An Introduction are included. ANALYTICAL CHEMISTRY FEATURES APPLICATIONS OF MICROSOFT® EXCEL IN ANALYTICAL CHEMISTRY, 2E F. James Holler, University of Kentucky; Stanley R Crouch, Michigan State University This supplement can be used in any analytical chemistry course. The exercises teach students how to use Microsoft® Excel® using applications from statistics, data analysis equilibrium calculations, curve fitting, and more. Operations include everything from basic arithmetic and cell formatting to Solver, Goal Seek, and the Data

Analysis Toolpak. The authors show students how to use a spreadsheet to construct log diagrams and to plot the results. Statistical data treatment includes descriptive statistics, linear regression, hypothesis testing, and analysis of variance. Tutorial exercises include nonlinear regression such as fitting the Van Deemter equation, fitting kinetics data, determining error coefficients in spectrophotometry, and calculating titration curves. Additional features include solving complex systems of equilibrium equations and advanced graphical methods: error bars, charts with insets, matrices and determinants, and much more. NEW TO THIS EDITION • The description and instructions were completely changed from those of Excel 2003 to Excel 2010 (2007). • There is now a better coordination with Skoog, Fundamentals of Analytical Chemistry, 9e in terms 36 • Exercises teach students how to use Microsoft® Excel® with applications from statistics, data analysis equilibrium calculations,

curve fitting, and more. • Operations include everything from basic arithmetic and cell formatting to Solver, Goal Seek, and the Data Analysis Toolpak. • The authors show students how to use a spreadsheet to construct log diagrams and to plot the results. • Statistical data treatment includes descriptive statistics, linear regression, hypothesis testing, and analysis of variance. • Tutorial exercises include nonlinear regression such as fitting the Van Deemter equation, fitting kinetics data, determining error coefficients in spectrophotometry, and calculating titration curves. CONTENTS 1. Excel Basics2 Basic Statistical Analysis with Excel.3 Statistical Tests with Excel4 Least-Squares and Calibration Methods.5 Equilibrium, Activity and Solving Equations.6 The Systematic Approach to Equilibria: Solving Many Equations.7 Neutralization Titrations and Graphical Representations.8 Polyfunctional Acids and Bases.9 Complexometric and Precipitation Titrations.10 Potentiometry and Redox

Titrations.11 Dynamic Electrochemistry12 Spectrochemical Methods.13 Kinetic Methods14 Chromatography.15 Electrophoresis and Other Separation Methods.16 Data Processing with Excel. 2014, 480pp, Paperback, 9781285087955 www.cengageasiacom Source: http://www.doksinet • • CTE FUNDAMENTALS OF ANALYTICAL CHEMISTRY WITH CB COURSESMART EBOOK, 9E • • • • Douglas A. Skoog, Stanford University; Donald M West, San Jose State University; F. James Holler, University of Kentucky; Stanley R. Crouch, Michigan State University • Please note that the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies.Known for its readability and systematic, rigorous approach, this fully updated Ninth Edition of FUNDAMENTALS OF ANALYTICAL

CHEMISTRY offers extensive coverage of the principles and practices of analytic chemistry and consistently shows students its applied nature. The book’s award-winning authors begin each chapter with a story and photo of how analytic chemistry is applied in industry, medicine, and all the sciences. To further reinforce student learning, a wealth of dynamic photographs by renowned chemistry photographer Charlie Winters appear as chapter-openers and throughout the text. • NEW TO THIS EDITION • OWL (Online Web Learning) is available for the first time with this Ninth Edition. OWL includes parameterized Mastery homework assignments correlated to sections in the text and parameterized end-of-chapter questions. OWL encourages students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes the interactive customizable Cengage YouBook and an optional Solutions Manual

eBook. All chapters have been rewritten for Excel 2010 (or 2007). A new Chapter 29 on Mass Spectrometry incorporates atomic mass spectrometry (formerly in Chapter 28) with new material on molecular mass spectrometry. New end-of-chapter problems have been added. All examples are now titled for easy reference. New Feature Boxes appear throughout, such as Feature 14-4 on the Master Equation. Approach Chapter 17 has a new section on Precipitation Titrations. In Chapter 25, the discussion on thermal IR detectors now puts more emphasis on the DTGS pyroelectric detector. Part VII on Practical Aspects of Chemical Analysis is now online to make it easier for students to access the material on preparing and analyzing real samples. CONTENTS 1. The Nature of Analytical ChemistryPART I: TOOLS OF ANALYTICAL CHEMISTRY2. Chemicals, Apparatus, and Unit Operations of Analytical Chemistry3. Using Spreadsheets in Analytical Chemistry 4. Calculations Used in Analytical Chemistry 5. Errors in Chemical

Analyses 6. Random Errors in Chemical Analysis7 Statistical Data Treatment and Evaluation 8. Sampling, Standardization, and Calibration PART II: CHEMICAL EQUILIBRIA9. Aqueous Solutions and Chemical Equilibria 10. Effect of Electrolytes on Chemical Equilibria 11. Solving Equilibrium Problems for Complex Systems PART III: CLASSICAL METHODS OF ANALYSIS12. Gravimetric Methods of Analysis13. Titrimetric Methods; Precipitation Titrimetry 14. Principles of Neutralization Titrations15. Titration Curves for Complex Acid/ Bases Systems16. Applications of Neutralization Titrations 17. Complexation Reactions and Titrations PART IV: ELECTROCHEMICAL METHODS 18. Introduction to Electrochemistry19. Applications of Standard Electrode Potentials20. Applications of Oxidation/Reduction Titrations 21. Potentiometry22 www.cengageasiacom 37 Source: http://www.doksinet Bulk Electrolysis: Electrogravimetry and Coulometry 23. Voltammetry PART V: SPECTROCHEMICAL ANALYSIS 24. Introduction to Spectrochemical

Methods 25. Instruments for Optical Spectroscopy26 Molecular Absorption Spectroscopy27. Molecular Fluorescence Spectroscopy28. Atomic Spectroscopy29. Mass SpectrometryPART VI: KINETICS AND SEPARATIONS 30. Kinetic Methods of Analysis31. Introduction to Analytical Separations 32. Gas Chromatography 33 High-Performance Liquid Chromatography 34. Miscellaneous Separation MethodsPART VII: PRACTICAL ASPECTS OF CHEMICAL ANALYSIS To access the following online-only chapters, enter ISBN 978-0-495-55828-6 at www.cengagebrain com and visit this book’s companion website.35 Analysis of Real Samples 36. Preparing Samples for Analysis 37. Decomposing and Dissolving the Sample 38. Selected Methods of Analysis 2014, 744pp, Paperback, 9789814591447 BIOCHEMISTRY BIOCHEMISTRY, INTERNATIONAL EDITION, 5E Reginald H. Garrett, University of Virginia; Charles M Grisham, University of Virginia Continuing Garrett and Grisham’s innovative conceptual and organizing “Essential Questions” framework,

BIOCHEMISTRY, 5E, International Edition guides students through course concepts in a way that reveals the beauty and usefulness of biochemistry in the everyday world. Offering a balanced and streamlined presentation, this edition has been updated throughout with new material and revised presentations. For the first time, this book is integrated with OWL, a powerful online learning system for chemistry that engages students and improves learning outcomes. NEW TO THIS EDITION • Revised Art and Graphics: To increase the pedagogical effectiveness of the art program and to help students better visualize chemical processes, the book’s molecular art has been revised to allow for greater consistency in use of atomic color code and now includes more current PyMOL-based molecular graphics. • New End-of-Chapter Material: A new “Things You Should Know” study section has been added to the end-of-chapter material. In addition, new topical headers in the problem sets make it easier to

assign problems that pertain to a particular topic. • New Coverage: New material has been added on the Ventor Institute’s creation of synthetic life; new discussions of protein sectors and metamorphic proteins have been added to Chapter 6; and 38 www.cengageasiacom Source: http://www.doksinet various free online protein databases have been incorporated throughout the book’s narrative. • Revised and Updated Coverage: This edition features thoroughly updated coverage of human gene therapy in Chapter 12 and heavily revised coverage of DNA metabolism in Chapter 28. • Reorganized Material: Material on reduction potentials and free energy changes in redox reactions has been placed earlier in the book (moved from Chapter 20 to Chapter 3); the discussion of protein techniques was moved from an appendix to Chapter 5 into the chapter proper as an “A Deeper Look” box; and the DNA Sequencing boxed essay is now expanded and incorporated into the Chapter 11 text narrative. •

Full Integration with OWL (Online Web Learning): For the first time, this book is fully integrated with OWL, a powerful online learning system for chemistry that engages students, assesses performance, and improves learning outcomes. OWL includes parameterized mastery homework assignments correlated to text sections that encourage students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes an interactive customizable Cengage YouBook (OWL’s multimedia e-book). FEATURES • Each chapter in this book is framed around an Essential Question that engages students in the material and encourages curiosity about the subject matter. • Human Biochemistry essays emphasize the central role of basic biochemistry in medicine and the health sciences with information on clinically important issues such as diet, diabetes, and cardiovascular health. • Critical Developments in

Biochemistry essays emphasize recent and historical advances in the field, while A Deeper Look essays expand on the text, highlighting selected topics or experimental observations. • End-of-chapter summaries review and briefly answer the key questions posed in each section. CONTENTS Part I: MOLECULAR COMPONENTS OF CELLS.1 Chemistry is the Logic of Biological Phenomena.2 WaterThe Medium of Life3 Thermodynamics of Biological Systems.4 Amino Acids.5 Proteins: Their Primary Structure and Biological Functions.6 Proteins: Secondary, Tertiary, and Quaternary Structure.7 Carbohydrates and Glyco-Conjugates of the Cell Surface.8 Lipids 9. Membranes and Membrane Transport10 Nucleotides and Nucleic Acids.11 Structure of Nucleic Acids.12 Recombinant DNA: Cloning and Creation of Chimeric Genes.Part II: PROTEIN DYNAMICS.13 Enzyme Kinetics14 Mechanisms of Enzyme Action.15 Enzyme Regulation16 Molecular Motors.Part III: METABOLISM AND ITS REGULATION.17 Nutrition and the Organization of Metabolism.18

Glycolysis19 The Tricarboxylic Acid Cycle.20 Electron Transport and Oxidative Phosphorylation.21 Photosynthesis22 Gluconeogenesis, Glycogen Metabolism, and the Pentose Phosphate Pathway.23 Fatty Acid Catabolism.24 Lipid Biosynthesis25 Nitrogen Acquisition and Amino Acid Metabolism.26 The Synthesis and Degradation of Nucleotides.27 Metabolic Integration and Organ Specialization. Part IV: INFORMATION TRANSFER.28 DNA Metabolism.29 Transcription and the Regulation of Gene Expression.30 Protein Synthesis31 PostTranslational Processing of Proteins and Protein Degradation.32 The Reception and Transmission of Extracellular Information. 2013, 1280pp, Paperback, 9781133108795 www.cengageasiacom 39 Source: http://www.doksinet in Biochemistry” now reflect the latest advances in the field. Count on BIOCHEMISTRY, 8th Edition, to lead the way in currency, clarity, and innovation for your one-semester biochemistry course NEW TO THIS EDITION CTE BIOCHEMISTRY WITH CB COURSESMART EBOOK, 8E Mary

K. Campbell, Mount Holyoke College; Shawn O Farrell, Olympic Training Center Please note that the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies.Introduce your students to the latest developments in biotechnology and genomics with this new edition of Campbell and Farrell’s bestselling text for the one-term course. Known for its logical organization, appropriate depth of coverage, and vibrant illustrations, BIOCHEMISTRY, 8th Edition, helps your students synthesize the flood of information that has inundated the field since the decoding of the human genome, while showing them how biochemistry principles connect to their everyday lives. The book incorporates up-to-date developments in stem cell research, cloning, and

immunology and offers revised coverage of major topics, such as Molecular Biology. Balancing scientific detail with readability, the book is ideal for students studying biochemistry for the first time. For example, in-text questions and problem sets categorized by problem type help students master chemistry and prepare for exams, and “Biochemical Connections” demonstrate how biochemistry applies to other fields such as health and sports medicine. In addition, the book’s revised state-ofthe-art visual program improves learning outcomes and its innovative magazine articles, “Hot Topics 40 • The #1 online homework and learning system for chemistry, OWLv2, is available for this textnow with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook;

Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader™, a new eBook with apps and embedded video, audio, annotations, and activities. OWLv2 courses for Gen Chem, GOB, and Liberal Arts now include Quick Prep essential skills assignments that can be taken before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text and new iPad-compatible visualizations, tutorials, and simulations. • New Hot Topics articles featured in Biochemistry Magazine Insert: The Hop Topics in Biochemistry Magazine which is bound inside the printed book and available online in the MindTap Reader features 15 articles that are hot topics in the biochemistry field right now. 8 articles are available in the printed book, and 7 extra articles are available in MindTap. The Hot Topics are great for in class discussions,

or can be assigned as student presentations. The hot topics show how biochemistry is relevant and important to our lives-after all biochemistry is the chemistry of the human body. • Hot Topics in Biochemistry Magazine: Green Fluorescent Protein: Jellyfish and Green Monkeys, DNA and Family Trees: Who is a Relative, Diabetes: An epidemic for Modern Times, Just One Word: Nanotechnology, Small, Smaller, Smallest: Beyond the Electron Microscope to Single Molecules, HPV Vaccines: Waging the War www.cengageasiacom Source: http://www.doksinet on Cervical Cancer, Stem Cells: Hype or Hope?, Doping in Sports: Good Science Gone Bad, Aging – Looking for the Biochemical Fountain of Youth, The Science of Happiness and Depression, Humans vs. Flu, Malaria, G-Protein-Coupled Receptors, The Genetics of Breast Cancer, and Proteins and Magnets: Nuclear Magnetic Resonance in Biochemistry. • NEW BIOCHEMICAL CONNECTIONS. Several new Biochemical Connections demonstrate how biochemistry topics relate

to the real world in high-interest areas such as allied health, sports medicine, and biotechnology. Biochemical Connections are now flowed in with the text where they are relevant to the conversation. These are meant to be read with the narrative, but they have a special design and magazine style voice to liven up the narrative! These are like crescendos in the narrative that keep student interest at a high level, and show them how biochemistry is a part of them and their daily lives. • New Marginal Glossary! Per student and faculty requests we added a marginal glossary to each page making it easier for students to learn key terms and understand concepts while reading the narrative. 22. Photosynthesis 23 The Metabolism of Nitrogen 24. Integration of Metabolism: Cellular Signaling Answers. Glossary Index 2015, Paperback, 9789814624244 CONTENTS 1. Biochemistry and the Organization of Cells 2 Water: The Solvent for Biochemical Reactions. 3 Amino Acids and Peptides. 4 The

Three-Dimensional Structure of Proteins. 5 Protein Purification and Characterization Techniques. 6 The Behavior of Proteins: Enzymes. 7 The Behavior of Proteins: Enzymes, Mechanisms, and Control. 8 Lipids and Proteins Are Associated in Biological Membranes. 9 Nucleic Acids: How Structure Conveys Information. 10. Biosynthesis of Nucleic Acids: Replication 11 Transcription of the Genetic Code: The Biosynthesis of RNA. 12 Protein Synthesis: Translation of the Genetic Message. 13 Nucleic Acid Biotechnology Techniques. 14 Viruses, Cancer and Immunology 15. The Importance of Energy Changes and Electron Transfer in Metabolism. 16 Carbohydrates 17. Glycolysis 18 Storage Mechanisms and Control in Carbohydrate Metabolism. 19 The Citric Acid Cycle. 20 Electron Transport and Oxidative Phosphorylation. 21 Lipid Metabolism www.cengageasiacom 41 Source: http://www.doksinet NEW TO THIS EDITION GENERAL CHEMISTRY CTE CHEMISTRY FOR ENGINEERING STUDENTS WITH CB COURSESMART EBOOK, 3E Larry Brown,

Texas A&M University; Tom Holme, Iowa State University Please note that the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies.Enhanced with a remarkable number of new problems and applications, the Third Edition of CHEMISTRY FOR ENGINEERING STUDENTS provides a concise, thorough, and relevant introduction to chemistry that prepares learners for further study in any engineering field. Updated with even more questions and applications specifically geared toward engineering, the book emphasizes the connection between molecular properties and observable physical properties and the connections between chemistry and other subjects such as mathematics and physics. This new edition is now fully supported by OWL, the most widely-used

online learning system for chemistry. 42 • Access to the #1 online homework and learning system for chemistry, OWLv2, is packaged with this hybrid edition and now with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader™, a new eBook with apps and embedded video, audio, annotations, and activities. OWLv2 courses for Gen Chem, GOB, and Liberal Arts now include Quick Prep essential skills assignments that can be taken before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text and new iPad-compatible

visualizations, tutorials, and simulations. • NEW EOC Problems: Replaced several endof-chapter problems and added several end-ofchapter problems. • Updated art and design program! • Content Changes to based on chemistry in the news and technological advances that are of special important in the engineering field as related to chemistry. • In chapter 3 the authors changed the context for the entire chapter from explosions to biofuels. • In chapter 4 the authors replaced “Focus on Problem Solving” with a new style of problem for this feature that includes graphical reasoning. • In chapter 6 the authors changed the context for the entire chapter from light bulbs to trace analysis. • Added a discussion in Section 14.6 about the Fukushima reactor accident and the release of radioactivity from it. www.cengageasiacom Source: http://www.doksinet CONTENTS 1. Introduction to Chemistry2 Atoms and Molecules.3 Molecules, Moles, & Chemical Equations.4 Stoichiometry5 Gases6

The Periodic Table and Atomic Structure.7 Chemical Bonding and Molecular Structure.8 Molecules and Materials9 Energy and Chemistry.10 Entropy and the Second Law of Thermodynamics.11 Chemical Kinetics12 Chemical Equilibrium.13 Electrochemistry14 Nuclear Chemistry.Appendices 2015, 416pp, Paperback, 9789814624862 CTE CHEMISTRY WITH CB COURSESMART EBOOK, 9E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Susan A. Zumdahl, University of Illinois, Urbana-Champaign Please note that the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies.This fully updated Ninth Edition of Steven and Susan Zumdahl’s CHEMISTRY brings together the solid pedagogy, easy-to-use media, and interactive exercises that today’s instructors need

for their general chemistry course. Rather than focusing on rote memorization, CHEMISTRY uses a thoughtful approach built on problem-solving. For the Ninth Edition, the authors have added a new emphasis on critical systematic problem solving, new critical thinking questions, and new computer-based interactive examples to help students learn how to approach and solve chemical problems--to learn to think like chemists-so that they can apply the process of problem solving to all aspects of their lives. Students are provided with the tools to become critical thinkers: to ask questions, to apply rules and develop models, and to evaluate the outcome. In addition, Steven and Susan Zumdahl crafted ChemWork, an online program included in OWL Online Web Learning to support their approach, much as an instructor would offer support during office hours. ChemWork is just one of many study aids available with CHEMISTRY that supports the hallmarks of the textbook--a strong emphasis on models, real

world applications, visual www.cengageasiacom 43 Source: http://www.doksinet learning, and independent problem solving. NEW TO THIS EDITION • A NEW EMPHASIS ON SYSTEMATIC PROBLEM SOLVING now appears in the applications of dimensional analysis. • NEW CRITICAL THINKING QUESTIONS have been added throughout the text to emphasize the importance of conceptual learning. • NEW COMPUTER-BASED INTERACTIVE EXAMPLES force students to think through the example step-by-step rather than simply scan the written example in the text as many students do. New Interactive Examples are available in OWL Online Web Learning. In addition, key examples from the text have been made into Interactive Tutorial problems and are available to assign in the OWL program. • NEW CHEMWORK PROBLEMS have been added to the end-of-chapter problems throughout the text to test students’ understanding of core concepts. They can be worked as pencil-andpaper problems or in interactive form in OWL, where students who

solve a problem with no assistance can proceed directly to the answer and students who need help can get assistance through a series of hints. The hints in OWL-usually in the form of interactive questions that guide students through the problem-solving process--are modeled after the way an instructor would assist a student with homework problems during office hours. Students cannot derive the answer in OWL through pattern recognition; rather, they are encouraged to continue working though the hints to arrive at the answer. • NEW END-OF–CHAPTER QUESTIONS AND PROBLEMS have been added throughout the text. • THE REVISED AND UPDATED ART PROGRAM has been modified as needed, and new macro/ micro illustrations have been added. • A NEW SECTION ON LIMITING REACTANTS in Chapter 3, the treatment of stoichiometry, emphasizes calculating the amounts of products that can be obtained from each reactant. Students 44 are taught how to select a limiting reactant both by comparing the amounts of

reactants present and by calculating the amounts of products that can be formed by complete consumption of each reactant. • A NEW SECTION ON PHOTOELECTRON SPECTROSCOPY was added to Chapter 9 (Section 9.6) • ENHANCED OWL (ONLINE WEB LEARNING) INTEGRATION: For the Ninth Edition, OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes Student Self- Assessments, ChemWork problems, Interactive Examples from the text, the interactive customizable Cengage YouBook, a customizable iPad-compatible multimedia eBook, and an optional Solutions Manual eBook. • PROBLEM-SOLVING STRATEGY BOXES focus the student’s attention on the very important process of problem solving, helping them learn to think like chemists. www.cengageasiacom Source: http://www.doksinet CONTENTS 1. Chemical Foundations2

Atoms, Molecules, and Ions.3 Stoichiometry4 Types of Chemical Reactions and Solution Stoichiometry.5 Gases6 Thermochemistry.7 Atomic Structure and Periodicity.8 Bonding: General Concepts9 Covalent Bonding: Orbitals.10 Liquids and Solids.11 Properties of Solutions12 Chemical Kinetics.13 Chemical Equilibrium14 Acids and Bases.15 Acid-Base Equilibria16 Solubility and Complex Ion Equilibria.17 Spontaneity, Entropy, and Free Energy.18 Electrochemistry19 The Nucleus: A Chemist’s View.20 The Representative Elements.21 Transition Metals and Coordination Chemistry.22 Organic and Biological Molecules Appendix 1. Mathematical ProceduresA11 Exponential Notation.A12 LogarithmsA13 Graphing Functions.A14 Solving Quadratic Equations.A15 Uncertainties in Measurements Appendix 2. The Quantitative Kinetic Molecular Model.Appendix 3 Spectral AnalysisAppendix 4. Selected Thermodynamic DataAppendix 5 Equilibrium Constants and Reduction Potentials. A5.1 Values of Ka for Some Common Monoprotic Acids.A52

Stepwise Dissociation Constants for Several Common Polyprotic Acids.A53 Values of Kb for Some Common Weak Bases.A54 Ksp Values at 25 C for Common Ionic Solids.A55 Standard Reduction Potentials at 25 C (298K) for Many Common Half-Reactions.Appendix 6 SI Units and Conversion Factors.GlossaryAnswers to Selected Exercises. 2014, 752pp, Paperback, 9789814568715 www.cengageasiacom 45 Source: http://www.doksinet NEW TO THIS EDITION CTE GENERAL CHEMISTRY WITH CB COURSESMART EBOOK, 10E Darrell D. Ebbing, Wayne State University; Steven D Gammon, Western Washington University Please note that the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies.The tenth edition of this market-leading text has been substantially revised to meet

the rapidly changing instructional demands of GENERAL CHEMISTRY professors. Known for its carefully developed, thoroughly integrated, stepby-step approach to problem solving, GENERAL CHEMISTRY helps students master quantitative skills and build a lasting conceptual understanding of key chemical concepts. The tenth edition retains this hallmark approach and builds upon the conceptual focus through key new features and revisions. 46 • Beautiful new book design that is user friendly, but also conveys the sense of excitement surrounding chemistry that the author team wants students to see! • Heavily revised art and photography program that helps highlight the excitement of chemistry while explaining key concepts. New talking labels have been added to the art and photos. These talk students through the figure and explain what they are seeing--what they need to know. • A new pedagogical feature has been added to all of the examples that are woven throughout the book. The new feature

in the examples is called the “Gaining Mastery Toolbox.” Every tool box contains “Critical Concepts” and “Solution Essentials.” Critical Concepts are concepts from the relevant chapter that the student needs to know in order to work through the example. The Solution Essential segment features a list of information needed to solve the problem presented--for example, a student may need the periodic table, Avogadro’s number, etc. • Many new and revised end-of-chapter problems and questions including a new type of strategy problem. • TWO TIER questions are ones that ask a student a question and then they must choose the answer. The second tier question is where they choose why they chose that answer. Students often choose the correct answer but not the correct reason they answered it correctly, which reveals that they do not under the concept being demonstrated • New end of chapter “Check List for Review” feature--this new feature is presented in an easyto-follow

tabular format that includes a summary of facts and concepts, learning objectives, important terms, and key equations. This innovative presentation is organized by section. • Up-to-date coverage in every chapter of the latest changes in chemistry. www.cengageasiacom Source: http://www.doksinet CONTENTS Part I: BASICS OF CHEMISTRY.1 Chemistry and Measurement.2 Atoms, Molecules, and Ions.3 Calculations with Chemical Formulas and Equations.4 Chemical Reactions5 The Gaseous State.6 ThermochemistryPart II: ATOMIC AND MOLECULAR STRUCTURE.7 Quantum Theory of the Atom.8 Electron Configurations and Periodicity9 Ionic and Covalent Bonding.10 Molecular Geometry and Chemical Bonding Theory.Part III: STATES OF MATTER AND SOLUTIONS.11 States of Matter; Liquids and Solids.12 SolutionsPart IV: CHEMICAL REACTIONS AND EQUILIBRIUM.13 Rates of Reaction.14 Chemical Equilibrium15 Acids and Bases.16 Acid-Base Equilibria17 Solubility and Complex-Ion Equilibria.18 Thermodynamics and Equilibrium.19

ElectrochemistryPart V: NUCLEAR CHEMISTRY AND CHEMISTRY OF THE ELEMENTS.20 Nuclear Chemistry21 Chemistry of the Main-Group Elements.22 The Transition Elements and Coordination Compounds.23 Organic Chemistry.24 Polymer Materials: Synthetic and Biological.APPENDIXESAnswers to Exercises Answers to Concept Checks. Answers to SelfAssessment QuestionsAnswers to Selected OddNumbered Problems 2013, 792pp, Paperback, 9789814601146 www.cengageasiacom 47 Source: http://www.doksinet NEW TO THIS EDITION CTE CHEMISTRY WITH CB COURSESMART EBOOK, 10E Kenneth W. Whitten, University of Georgia; Raymond E Davis, University of Texas, Austin; Larry Peck, Texas A&M University; George G. Stanley, Louisiana State University Please note that the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and

tools to help you take notes and organize your studies.This new edition of CHEMISTRY continues to incorporate a strong molecular reasoning focus, amplified problem-solving exercises, a wide range of reallife examples and applications, and innovative technological resources. With this text’s focus on molecular reasoning, readers will learn to think at the molecular level and make connections between molecular structure and macroscopic properties. The Tenth Edition has been revised throughout and now includes a reorganization of the descriptive chemistry chapters to improve the flow of topics, a new basic math skills Appendix, an updated art program with new “talking labels” that fully explain what is going on in the figure, and much more. 48 • REORGANIZATION OF DESCRIPTIVE CHEMISTRY CHAPTERS (22-28): To facilitate an improved flow of the descriptive chemistry topics optionally covered in many courses and to provide more convenient options for custom versions of the textbook,

Chapters 22 through 28 have been reorganized as follows: Chapter 22 is now Nuclear Chemistry; Chapter 23, Organic Chemistry I: Formulas, Names and Properties; Chapter 24, Organic Chemistry II: Shapes, Selected Reactions, and Biopolymers; Chapter 25, Coordination Compounds; Chapter 26, Metals I: Metallurgy; Chapter 27, Metals II: Properties and Reactions; and Chapter 28, Some Nonmetals and Metalloids. • NEW BASIC MATH SKILLS APPENDIX: To aid the flow of introductory chemistry material in Chapter 1, a review of topics in basic mathematics skills, including scientific notation and use of significant figures, with numerous Examples, now appears in Appendix A. Related Exercises remain in the Measurements and Calculations area at the end of Chapter 1. • MORE COMPREHENSIVE COVERAGE OF CENTRAL ATOM LONE PAIRS: In Chapter 8, a more comprehensive tabular summary of the influence of central atom lone pairs on molecular geometry has been added to enhance student understanding. • A REVISED

AND UPDATED ART PROGRAM: The Tenth Edition’s art program has been revised to include “talking labels” placed strategically within figures to explain what is going on in the illustration, so students can focus on learning instead of trying to figure out what is going on by going back and forth between a caption and the art. To exemplify the beauty and excitement of chemistry, the individual layouts of many figures have been revised to be more visually pleasing, balanced, and organized. The art program now includes more molecular models generated by the latest software to enhance the molecular reasoning theme. All electrostatic charge potential (ECP) art includes a more thorough explanation of its use. www.cengageasiacom Source: http://www.doksinet • ENHANCED OWL ONLINE WEB LEARNING: For the Tenth Edition, OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and

numbers to ensure their mastery of the underlying chemical concepts. OWL also includes the Cengage YouBook, a customizable iPad-compatible multimedia eBook, Quick Prep assignments that help students learn skills essential for success in General Chemistry, and an optional solutions manual eBook. FEATURES • REORGANIZED INTRODUCTION TO AQUEOUS SOLUTIONS: Section 6-1 has been reorganized to improve the descriptive introduction to aspects of aqueous solutions, including ionization and dissociation, acids, bases, and solubility guidelines. These basic ideas are then elaborated in the classification of reactions in the remainder of Chapter 6 and serve as a foundation throughout the textbook for further discussion of physical and chemical properties of solutions. • MOLECULAR REASONING AND VISUALIZATION EMPHASIS: Molecular reasoning is woven throughout the text in chapter objectives, chapter essays, examples, and end-of-chapter problems and highlighted by a molecular reasoning icon.

Chemistry I: Formulas, Names and Properties.24 Organic Chemistry II: Shapes, selected Reactions, and Biopolymers.25 Coordination Compounds26 Metals I: Metallurgy.27 Metals II: Properties and Reactions.28 Some Nonmetals and Metalloids Appendix A: Basic Math Skills (includes new significant figure section).Appendix B: Electron Configurations of the Atoms of the Elements. Appendix C: Common Units, Equivalences, and Conversion Factors.Appendix D: Physical Constants.Appendix E: Some Physical Constants for a Few Common Substances.Appendix F: Ionization Constants for Weak Acids at 25°C. Appendix G: Ionization Constants for Weak Bases at 25°C.Appendix H: Solubility Product Constants for Some Inorganic Compounds at 25°C.Appendix I: Dissociation Constants for Some Complex Ions. Appendix J: Standard Reduction Potentials in Aqueous Solution at 25°C.Appendix K: Selected Thermodynamic Values at 298.15 KAppendix L: Answers to Selected Even-Numbered Numerical Exercises.Index of

EquationsGlossary/Index 2014, 792pp, Paperback, 9789814601368 CONTENTS 1. The Foundations of Chemistry2 Chemical Formulas and Composition Stoichiometry.3 Chemical Equations and Reaction Stoichiometry.4 The Structure of Atoms.5 Chemical Periodicity6 Some Types of Chemical Reactions.7 Chemical Bonding.8 Molecular Structure and Covalent Bonding Theories.9 Molecular Orbitals in Chemical Bonding.10 Reactions in Aqueous Solutions I: Acids, Bases, and Salts.11 Reactions in Aqueous Solutions II: Calculations.12 Gases and the Kinetic-Molecular Theory.13 Liquids and Solids14 Solutions.15 Chemical Thermodynamics16 Chemical Kinetics.17 Chemical Equilibrium18 Ionic Equilibria I: Acids and Bases.19 Ionic Equilibria II: Buffers and Titration Curves.20 Ionic Equilibria III: The Solubility Product Principle.21 Electrochemistry.22 Nuclear Chemistry23 Organic www.cengageasiacom 49 Source: http://www.doksinet CTE CHEMISTRY AND CHEMICAL REACTIVITY WITH CB COURSESMART EBOOK, 9E • Please note that

the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies. Succeed in chemistry with the clear explanations, problem-solving strategies, and dynamic study tools of CHEMISTRY & CHEMICAL REACTIVITY, 9e. Combining thorough instruction with the powerful multimedia tools you need to develop a deeper understanding of general chemistry concepts, the text emphasizes the visual nature of chemistry, illustrating the close interrelationship of the macroscopic, symbolic, and particulate levels of chemistry. The art program illustrates each of these levels in engaging detail-and is fully integrated with key media components. In addition access to OWLv2 may be purchased separately or at a special price if packaged with this text. OWLv2 is an

online homework and tutorial system that helps you maximize your study time and improve your success in the course. OWLv2 includes an interactive eBook, as well as hundreds of guided simulations, animations, and video clips. • John C. Kotz, State University of New York, Oneonta; Paul M Treichel, University of Wisconsin, Madison; John Townsend, West Chester University of Pennsylvania; David Treichel, Nebraska Wesleyan University NEW TO THIS EDITION • The five topical interchapters in previous editions 50 • • have been integrated into standard chapters: Milestones in the Development of Chemistry and the Modern World View of Atoms and Molecules have been folded into Chapter 2. The Chemistry of Fuels and Energy Resources and The Chemistry of the Environment have been incorporated into an expanded new chapter on Environmental Chemistry (Chapter 20). The Chemistry of Life: Biochemistry has been expanded into a full chapter (Chapter 24). The Chemistry of Modern Materials has

been incorporated into the chapter on solids (Chapter 12). Chapter Goals (and Chapter Goals Revisited) have been recast into three categories that most express what students should get out of the course: 1. Understand: chapter concepts 2 Do: Be able to carry out calculations, draw molecular structures, and make chemical decisions. 3 Remember: important facts and chemical concepts. All answers are now combined into a single comprehensive appendix organized by chapter. Over 100 new end of chapter Study Questions have been added. The #1 online homework and learning system for chemistry, OWLv2, is available for this text-now with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts

and skills; and MindTap Reader™, a new eBook with apps and embedded video, audio, annotations, and activities. OWLv2 courses for Gen Chem, GOB, and Liberal Arts now include Quick Prep essential skills assignments that can be taken before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text and new iPad-compatible visualizations, tutorials, and simulations. CONTENTS PART I: CONCEPTS OF CHEMISTRY.1 Basic Concepts of Chemistry.Let’s Review: The Tools www.cengageasiacom Source: http://www.doksinet of Quantitative Chemistry.2 Atoms, Molecules, and Ions.3 Chemical Reactions4 Stoichiometry: Quantitative Information from Chemical Reactions.5 Principles of Chemical Reactivity: Energy and Chemical Reactions.PART II: ATOMS AND MOLECULES.6 The Structure of Atoms7 The Structure of Atoms and Periodic Trends.8 Covalent Bonding and Molecular

Structure.9 Bonding and Molecular Structure - Valence Bond and Molecular Orbital Theory.Part 3: States of Matter10 Gases and Their Properties.11 Intermolecular Forces and Liquids.12 Ionic Bonding, Metals, and the Solid State.13 Solutions and Their BehaviorPART IV: THE CONTROL OF CHEMICAL REACTIONS.14 Chemical Kinetics - The Rates of Chemical Reactions.15 Principles of Reactivity: Chemical Equilibria.16 Equlibria and Acids and Bases17 Principles of Reactivity: Other Aspects of Aqueous Equilibria.18 Thermodynamics - Entropy and Free Energy.19 Principles of Reactivity: Electron Transfer Reactions.PART V: THE CHEMISTRY OF THE ELEMENTS.20 Environmental Chemistry: Earth’s Environment, Energy, and Sustainability.21 The Chemistry of the Main Group Elements.22 The Chemistry of the Transition Elements.23 Carbon: Not Just Another Element.24 Biochemistry25 Nuclear Chemistry.Appendix A: Using Logarithms and the Quadratic Equation.Appendix B: Some Important Physical Concepts.Appendix C:

Abbreviations and Useful Conversion Factors.Appendix D: Physical Constants.Appendix E: Naming Organic Compounds.Appendix F: Values for the Ionization Energies and Electron Affinities of the Elements. Appendix G: Vapor Pressure of Water at Various Temperatures.Appendix H: Ionization Constants for Weak Acids at 25ºC.Appendix I: Ionization Constants for Weak Bases at 25ºC.Appendix J: Solubility Product Constants for Some Inorganic Compounds at 25ºC.Appendix K: Formation Constants for Some Complex Ions in Aqueous Solution.Appendix L: Selected Thermodynamic Values.Appendix M: Standard Reduction Potentials in Aqueous Solution at 25ºC.Appendix N: Answers to Chapter Opening and Case Study Questions, Check Your Understanding Questions, Review and Check Questions, and Selected Study Questions. 2015, 928pp, Paperback, 9789814617796 GENERAL CHEMISTRY (WITH MINDTAP CHEMISTRY 24-MONTHS PRINTED ACCESS CARD) William Vining, State University of New York at Oneonta; Susan Young, Assistant

Professor of Chemistry, University of Colorado at Boulder; Roberta Day, Professor Emeritus, University of Massachusetts; Beatrice Botch, University of Massachusetts, Amherst MindTap General Chemistry is a personalized teaching and learning experience that allows instructors to control what students see and focus on relevant assignments that guide them to analyze, apply, and improve thinking. Seamlessly integrating interactive simulations, videos and diagnostic quizzes, it helps students achieve course learning outcomes by bringing chemistry concepts to life. Measure skills and outcomes with ease using powerful analytics that provide a visual dashboard with at-a-glance performance and engagement data that is used to provide direction regarding class and student needs. This version is accompanied by a print text that includes the narrative from the MindTap General Chemistry course. FEATURES • Easily Set Your Own Course: Manage, administer and customize to meet your course needs. Do it

yourself or let us help. • Elevate Thinking: Use relevant activities that take students from basic knowledge and understanding to higher level learning. • Promote Better Outcomes: Track progress and know where students stand in class at all times. • Seamlessly deliver appropriate content and technology assets from a number of providers to students, as they need them. www.cengageasiacom 51 Source: http://www.doksinet • Break course content down into movable objects to promote personalization, encourage interactivity and ensure student engagement. • Customize the course – from tools to text – and make adjustments ‘on the fly,’ making it possible to intertwine breaking news into their lessons and incorporate today’s teachable moments. • Bring interactivity into learning through the integration of multimedia assets (apps from Cengage Learning and other providers), and numerous in-context exercises and supplements. Student engagement will increase, leading to

better student outcomes. • Track students’ use, activities and comprehension in real-time, which provides opportunities for early intervention to influence progress and outcomes. Grades are visible and archived so students and instructors always have access to current standings in the class. • Assess knowledge throughout each section: after readings, in activities, homework, and quizzes. • Automatically grade all homework and quizzes. and CompoundsStoichiometryChemical Reactions and Solution Stoichiometry ThermochemistryElectromagnetic Radiation and the Electronic Structure of the AtomElectron Configurations and the Properties of AtomsCovalent Bonding and Molecular StructureTheories of Chemical BondingGasesIntermolecular Forces and the Liquid StateThe Solid StateChemical Mixtures: Solutions and Other MixturesChemical KineticsChemical EquilibriumAcids and BasesAdvanced Acid-Base EquilibriaPrecipitation and Lewis Acid-Base EquilibriaThermodynamics: Entropy and Free

EnergyElectrochemistryHydrocarbonsApplying Chemical Principles to the Main Group ElementsThe Transition ElementsNuclear Chemistry 2015, 880pp, Paperback, 978130527515 CONTENTS The Learning Path guides students through the course. Instructors are provided a fully loaded version that consists of interactive content and exercises that can be reassembled and rearranged by the instructor. Instructors may also add their own content and assignments anywhere within the Learning Path and its readings.Instructional DesignMindTap for General Chemistry is designed to be used in the first year general chemistry course, and is comprised of twenty-two units. The Learning Path for each unit guides the students through the course. Each unit contains interactive narrative with assignable conceptual and problem solving activities, mastery questions, and challenge problems that will help students achieve conceptual understanding as well as master problem-solving skills. A study center tracks individual

student and overall class progress on course learning objectives and identifies where they need to focus their study time. Instructors can also add their own content anywhere in the Learning Path.Unit ListChemistry: Matter on the Atomic ScaleElements 52 www.cengageasiacom Source: http://www.doksinet FEATURES THE GUIDE TO SURVIVING GENERAL CHEMISTRY, 2E Michael Rosen Available packaged with any CENGAGE textbook, this helpful guide is a frontline resource for students who need extra help or want to improve their General Chemistry grade. Written by a student with extensive tutoring experience who understands where students struggle most and using terms that they most relate to and understand, this guide helps students see that they can actually master chemistry concepts. GUIDE TO SURVIVING GENERAL CHEMISTRY includes study tips and example problems with worked out solutions for all topics in general chemistry, and is endorsed by Professor Mark Oram, Ph.D, for accuracy and topic

coverage. This book is also available for students to purchase separately at www.CENGAGEbraincom • Saves instructors time by offering students a resource that they can use first to help answer questions before coming to see instructors for help. • Provides a front line resource for students who need extra help or want to improve their General Chemistry grade. • Written by a student for students, general chemistry topics are presented at a level that students can relate to and understand which gives students the confidence that they can learn general chemistry. • Offers effective study tips for learning general chemistry concepts. • Provides example problems and worked out solutions so that students can strengthen their problem-solving skills. CONTENTS 1. Acids and Bases2 Colligative Properties3 Concentration Unites and Conversions for Solutions.4 Dimensional Analysis and Significant Figures.5 Electrochemistry and Redox6 Electrons.7 Equilibrium Calculations8 Gas Laws9

Kinetics.10 Lewis Structures and VSEPR Theory11 Nomenclature.12 Organic chemistry13 Periodic Table.14 Phase Diagrams and Crystalline Solids15 Quantitative Calculations.16 Solubility and Net Ionic Equations.17 Statistics18 Thermodynamics 2015, 192pp, Paperback, 9781305391383 NEW TO THIS EDITION • The second edition has been edited by college chemistry professor, Dr Mark Oram. The book combines the legitimacy of a conventional textbook with the one-of-a-kind perspective of a student who understands the pitfalls of learning general chemistry. Bridging the gap between a professor’s level of understanding and that of a student is the hallmark of this unique survival guide. www.cengageasiacom 53 Source: http://www.doksinet CTE CHEMICAL PRINCIPLES WITH CB COURSESMART EBOOK, 7E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Donald J. DeCoste, University of Illinois, Urbana-Champaign Please note that the digital access code that comes with the print book is valid for

use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies.Develop the qualitative, conceptual foundation you need to think like a chemist with CHEMICAL PRINCIPLES, 7e. Designed for students with solid mathematical preparation, this best-seller offers a unique organization that emphasizes models, everyday applications of chemistry, and a thoughtful, stepby-step problem-solving approach. NEW TO THIS EDITION • New Co-author: Don DeCoste, brings his wealth of teaching experience to this exceptional Seventh Edition • New “Learning to Solve Problems” Section: A new Section 3.4 emphasizes the importance of conceptual problem solving by showing students how to think their way through a problem. This section discusses how to solve problems in a flexible, creative way based on understanding the

fundamental ideas of chemistry and asking and answering key questions. Students will learn that this “big picture approach” produces more long term, meaningful learning rather than simply memorizing specific steps that are easily forgotten. • New Chemical Insights Boxes: Many new and revised Chemical Insights boxes cover such up- 54 to-date topics as geoengineering, laser cooling, graphene, and nanogenerators. • New and Revised Problems: Many of the book’s end-of-chapter questions and problems have been revised and more than 50 new visual problems have been added. • New In-text Learning Aids. A list of Key Terms has been added at the end of each chapter along with an Outline that reviews each chapter. In addition, many of the book’s figures have been revised to better serve visual learners. FEATURES • Unique Organization: The authors cover equilibria and acid-base chemistry early and delay coverage of atomic theory and bonding until the second half of the text. The

text includes sections on Exact Treatment of Buffered Solutions (Chapter 8), Adiabatic Processes (Chapter 10), and Molecular, Rotational, Vibrational, Electronic, and Nuclear Magnetic Spectroscopy (Chapter 14). These sections provide more depth at a slightly more rigorous level, consistent with the book’s overall focus. CONTENTS 1. Chemists and Chemistry2 Atoms, Molecules, and Ions.3 Stoichiometry4 Types of Chemical Reactions and Solution Stoichiometry.5 Gases6 Chemical Equilibrium.7 Acids and Bases8 Applications of Aqueous Equilibria.9 Energy, Enthalpy, and Thermochemistry.10 Spontaneity, Entropy, and Free Energy.11 Electrochemistry12 Quantum Mechanics and Atomic Theory.13 Bonding: General Concepts.14 Covalent Bonding: Orbitals.15 Chemical Kinetics16 Liquids and Solids.17 Properties of Solutions18 The Representative Elements.19 Transition Metals and Coordination Chemistry.20 The Nucleus: A Chemist’s View.21 Organic and Biochemical Molecules.Appendix 1 Mathematical Procedures

Appendix 2. Units of Measurement and Conversions Among Units.Appendix 3 Spectral Analysis Appendix 4. Selected Thermodynamic Data Appendix 5. Equilibrium Constants and Reduction Potentials.GlossaryAnswers to Selected Exercises 2013, 832pp, Paperback, 9789814605083 www.cengageasiacom Source: http://www.doksinet NEW TO THIS EDITION CTE CHEMISTRY AND CHEMICAL REACTIVITY WITH CB COURSESMART EBOOK, 9E John C. Kotz, State University of New York, Oneonta; Paul M Treichel, University of Wisconsin, Madison; John Townsend, West Chester University of Pennsylvania; David Treichel, Nebraska Wesleyan University Please note that the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies. Succeed in chemistry with the clear explanations,

problem-solving strategies, and dynamic study tools of CHEMISTRY & CHEMICAL REACTIVITY, 9e. Combining thorough instruction with the powerful multimedia tools you need to develop a deeper understanding of general chemistry concepts, the text emphasizes the visual nature of chemistry, illustrating the close interrelationship of the macroscopic, symbolic, and particulate levels of chemistry. The art program illustrates each of these levels in engaging detail-and is fully integrated with key media components. In addition access to OWLv2 may be purchased separately or at a special price if packaged with this text. OWLv2 is an online homework and tutorial system that helps you maximize your study time and improve your success in the course. OWLv2 includes an interactive eBook, as well as hundreds of guided simulations, animations, and video clips. • The five topical interchapters in previous editions have been integrated into standard chapters: Milestones in the Development of

Chemistry and the Modern World View of Atoms and Molecules have been folded into Chapter 2. The Chemistry of Fuels and Energy Resources and The Chemistry of the Environment have been incorporated into an expanded new chapter on Environmental Chemistry (Chapter 20). The Chemistry of Life: Biochemistry has been expanded into a full chapter (Chapter 24). The Chemistry of Modern Materials has been incorporated into the chapter on solids (Chapter 12). • Chapter Goals (and Chapter Goals Revisited) have been recast into three categories that most express what students should get out of the course: 1. Understand: chapter concepts 2 Do: Be able to carry out calculations, draw molecular structures, and make chemical decisions. 3 Remember: important facts and chemical concepts. • All answers are now combined into a single comprehensive appendix organized by chapter. • Over 100 new end of chapter Study Questions have been added. • The #1 online homework and learning system for chemistry,

OWLv2, is available for this text-now with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader™, a new eBook with apps and embedded video, audio, annotations, and activities. OWLv2 courses for Gen Chem, GOB, and Liberal Arts now include Quick Prep essential skills assignments that can be taken before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text and new iPad-compatible visualizations, tutorials, and simulations. www.cengageasiacom 55 Source: http://www.doksinet CONTENTS PART I: CONCEPTS OF

CHEMISTRY.1 Basic Concepts of Chemistry.Let’s Review: The Tools of Quantitative Chemistry.2 Atoms, Molecules, and Ions.3 Chemical Reactions4 Stoichiometry: Quantitative Information from Chemical Reactions.5 Principles of Chemical Reactivity: Energy and Chemical Reactions.PART II: ATOMS AND MOLECULES.6 The Structure of Atoms7 The Structure of Atoms and Periodic Trends.8 Covalent Bonding and Molecular Structure.9 Bonding and Molecular Structure - Valence Bond and Molecular Orbital Theory.Part 3: States of Matter10 Gases and Their Properties.11 Intermolecular Forces and Liquids.12 Ionic Bonding, Metals, and the Solid State.13 Solutions and Their BehaviorPART IV: THE CONTROL OF CHEMICAL REACTIONS.14 Chemical Kinetics - The Rates of Chemical Reactions.15 Principles of Reactivity: Chemical Equilibria.16 Equlibria and Acids and Bases17 Principles of Reactivity: Other Aspects of Aqueous Equilibria.18 Thermodynamics - Entropy and Free Energy.19 Principles of Reactivity: Electron Transfer

Reactions.PART V: THE CHEMISTRY OF THE ELEMENTS.20 Environmental Chemistry: Earth’s Environment, Energy, and Sustainability.21 The Chemistry of the Main Group Elements.22 The Chemistry of the Transition Elements.23 Carbon: Not Just Another Element.24 Biochemistry25 Nuclear Chemistry.Appendix A: Using Logarithms and the Quadratic Equation.Appendix B: Some Important Physical Concepts.Appendix C: Abbreviations and Useful Conversion Factors.Appendix D: Physical Constants.Appendix E: Naming Organic Compounds.Appendix F: Values for the Ionization Energies and Electron Affinities of the Elements. Appendix G: Vapor Pressure of Water at Various Temperatures.Appendix H: Ionization Constants for Weak Acids at 25ºC.Appendix I: Ionization Constants for Weak Bases at 25ºC.Appendix J: Solubility Product Constants for Some Inorganic Compounds at 25ºC.Appendix K: Formation Constants for Some Complex Ions in Aqueous Solution.Appendix L: Selected Thermodynamic Values.Appendix M: Standard Reduction

Potentials in Aqueous Solution at 25ºC.Appendix N: Answers to Chapter Opening and Case Study Questions, 56 Check Your Understanding Questions, Review and Check Questions, and Selected Study Questions. 2015, 928pp, Paperback, 9789814617796 CHEMISTRY, 2E An Atoms First Approach Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Susan A. Zumdahl, University of Illinois, Urbana-Champaign Steve and Susan Zumdahl’s texts focus on helping students build critical thinking skills through the process of becoming independent problem-solvers. They help students learn to “think like chemists” so they can apply the problem-solving process to all aspects of their lives. In this Second Edition of CHEMISTRY: AN ATOMS FIRST APPROACH, the Zumdahls use a meaningful approach that begins with the atom and proceeds through the concept of molecules, structure, and bonding to more complex materials and their properties. Because this approach differs from what most students have

experienced in high school courses, it encourages them to focus on conceptual learning early in the course, rather than relying on memorization and a “plug and chug” method of problem solving that even the best students can fall back on when confronted with familiar material. The atoms first organization provides an opportunity for students to use the tools of critical thinkers: to ask questions, to apply rules and models, and to evaluate outcomes. NEW TO THIS EDITION • REORGANIZED www.cengageasiacom FOR ENHANCED Source: http://www.doksinet • • • • • UNDERSTANDING: A reorganization of key chapters (3, 4, 5, and 6) allows for stoichiometry to be taught earlier (Chapter 5), which coincides with labs being done at that time. In addition, the organization of various sections has been finetuned (for example, the Gas Stoichiometry section moved to the Gases chapter and the Calorimetry section moved to the Chemical Energy chapter). The combined chapter and section

reorganization improves the flow of the text to better meet the needs of those teaching and learning from an atoms first approach. NEW “CRITICAL THINKING” QUESTIONS provide a greater emphasis on the importance of conceptual learning. NEW CHEMWORK EXERCISES, which can be worked using the online system or as pencil-andpaper problems, test students’ understanding of core chapter concepts. NEW ATOMS FIRST MARGIN NOTES throughout the text enhance teaching and learning using an atoms first approach. NEW ATOMS FIRST BOXED FEATURES “CONNECTING TO ATOMS” help students understand how varying chapter content works together under an atoms first approach through a summary of key concepts at point-of-use, which provides both a review of atoms first concepts and a glimpse of what is ahead. ENHANCED ONLINE LEARNING: The #1 online homework and learning system for chemistry, OWLv2, is available for this text--and now features more flexible student and instructor functionality, new personalized

study tools, enhanced integration with learning management systems, and improved analytics. OWLv2 for this text also includes Quick Prep, an online short course that reviews key chemistry concepts and essential skills, new Adaptive Study Plans, hundreds of new interactive versions of the text’s end-of-chapter questions, and new tutors, visualizations, and simulations that have been converted from Flash to HTML, allowing for easier navigation and streamlined grading. FEATURES • AN ATOMS FIRST APPROACH: By taking an atoms first approach, the authors provide students with a unified story built around an organizing principle--start the course with the smallest element, the atom, and build from there. Building their explanations around this structure, the authors consistently show the importance and relevance of studying chemistry. • A FOCUS ON CONCEPTUAL UNDERSTANDING: Rather than focusing on memorizing, the book gives students the tools they need to become critical thinkers: to

ask questions, to apply rules and develop models, and to evaluate the outcome. • A STRONG PROBLEM-SOLVING ORIENTATION: Throughout the text, problem-solving strategies help students learn to solve problems by thinking them through rather than brute-force memorizing. Section 5.3 “Learning to Solve Problems” emphasizes the importance of thoughtful, creative problem solving, demonstrating that thinking through a problem produces more long-term, meaningful learning that can be applied to “real life” than memorizing steps that apply only to a particular type of problem. The problem-solving process is organized in terms of “Where are we going?”; “How do we get there?”; and “Reality Check,” which prompts students to check whether their answer makes sense. • STUDENT-ORIENTED LEARNING AIDS: Problem-solving strategy boxes help students focus on particular aspects of problem-solving; concept summary boxes help students organize their thinking about crucial concepts;

criticalthinking questions help students to contemplate various atoms first concepts; chemical connections boxes present applications of chemistry in various fields and in daily life; and atoms first boxes provide an overall summary at critical junctures that ties together concepts to enhance student understanding. CONTENTS Review: Measurement and Calculations in Chemistry.1 Chemical Foundations2 Atomic Structure and Periodicity.3 Bonding: General Concepts.4 Molecular Structure and Orbitals5 Stoichiometry.6 Types of Chemical Reactions and Solution Stoichiometry.7 Chemical Energy8 Gases.9 Liquids and Solids10 Properties of Solutions.11 Chemical Kinetics12 Chemical www.cengageasiacom 57 Source: http://www.doksinet Equilibrium.13 Acids and Bases14 Acid-Base Equilibria15. Solubility and Complex Ion Equilibria16 Spontaneity, Entropy, and Free Energy.17 Electrochemistry.18 The Nucleus: A Chemist’s View.19 The Representative Elements20 Transition Metals and Coordination Chemistry.21

Organic and Biological Molecules. • 2016, 1216pp, Hardback, 9781305079243 • • CHEMISTRY, 8E • Principles and Reactions William L. Masterton, University of Connecticut, Emeritus; Cecile N. Hurley, University of Connecticut This latest edition of CHEMISTRY: PRINCIPLES AND REACTIONS takes students directly to the crux of chemistry’s fundamental concepts and allows you to efficiently cover all topics found in a typical general chemistry book. Based on the authors’ extensive teaching experience, the book includes rigorous graded and concept-driven examples, as well as examples that focus on molecular reasoning and understanding. The Eighth Edition features a new and innovative example format, new “talking labels” within artwork, 25% new or revised problems, “Chemistry: Beyond the Classroom” essays that highlight some of the most up-to-date uses of chemistry, and end-of-chapter questions and Key Concepts that correlate to OWLv2, the #1 online homework and

tutorial system for chemistry. NEW TO THIS EDITION • NEW AND INNOVATIVE EXAMPLE FORMAT: Clear, consistent, and easy to follow, the new 58 • • • Example format includes analysis, strategy, and solution sections after each individual part of the Example. Each example ends with an End Point, which provides additional insight into the problem. NEW “TALKING LABELS”: This edition moves relevant text from captions to talking labels within the art for a clearer presentation of visual images. Contemporary photographs, modern molecular models, and new concept flowcharts help further clarify key concepts. MORE FLOWCHARTS: Owing to the enthusiastic response to them in the last edition, more flowcharts have been added and existing ones revised to help students visualize a pathway to follow for various topics. BALANCING REDOX EQUATIONS MOVED TO CHAPTER 17: In response to instructor and reviewer feedback, the discussion of balancing redox equations has been moved from Chapter 4 to

Chapter 17 and redox reactions are treated in Chapter 4 only as far as stoichiometric calculations are involved (balanced equations are provided for these reactions). 25% NEW AND REVISED PROBLEMS: To keep the end-of-chapter questions fresh, approximately 25% of the problems are either new or revised. NEW AND REVISED SUMMARY PROBLEMS: Almost all of the summary problems have either been revised or are completely new to this edition. NEW CHAPTER-OPENING ARTWORK: Almost all of the fine art used in the chapter-opening images to illustrate chemical principles and applications is new. ENHANCED ONLINE LEARNING: The most powerful online learning solution for chemistry is better than ever. OWLv2 now has more flexible student and instructor functionality, new personalized study tools, enhanced integration with learning management systems, and improved analytics. For this course, OWLv2 also includes Quick Prep, an online short course to review key chemistry concepts and essential skills, new

Adaptive Study Plans, and new iPad-compatible visualizations, tutorials, and simulations that have been converted from Flash to HTML, allowing for easier navigation and streamlined grading. www.cengageasiacom Source: http://www.doksinet FEATURES • CONNECTION TO FINE ARTS: The text connects the hard science of chemistry to the humanities and fine arts through chapter openers and literary quotations that enhance each chapter’s content. • LATEST WORK FROM SPECIALISTS: Guest authors and leaders in specialized fields profile the latest research in “Chemistry: Beyond the Classroom” boxes. Students see the relevance of concepts in some of the most current work in chemistry, including coloration of biological organisms, molecular structure of rubbery materials, and fuel cells. CONTENTS 1. Matter and Measurements2 Atoms, Molecules, and Ions.3 Mass Relations in Chemistry; Stoichiometry.4 Reactions in Aqueous Solution5 Gases.6 Electronic Structure and the Periodic Table.7 Covalent

Bonding8 Thermochemistry9 Liquids and Solids.10 Solutions11 Rate of Reaction.12 Gaseous Chemical Equilibrium13 Acids and Bases.14 Equilibria in Acid-Base Solutions.15 Complex ion and Precipitation Equilibria.16 Spontaneity of Reaction17 Electrochemistry.18 Nuclear Reactions19 Complex Ions and Coordination Compounds.20 Chemistry of the Metals.21 Chemistry of the Nonmetals.22 Organic Chemistry23 Organic Polymers, Natural and Synthetic.Appendix 1 Units, Constants, and Reference Data.Appendix 2 Properties of the Elements.Appendix 3 Exponents and Logarithms.Appendix 4 Molecular Orbitals Appendix 5. Answers to Even-Numbered and Challenge Questions and Problems.Index/Glossary LAB MANUAL FOR ZUMDAHL/ ZUMDAHL’S CHEMISTRY: AN ATOMS FIRST APPROACH, 2ND, 2E Charles H. Atwood, University of Georgia Build skill and confidence in the lab with the experiments included in this manual. Safety is strongly emphasized. 2016, 624pp, Paperback, 9781305398313 2016, 800pp, Hardback, 9781305079373

www.cengageasiacom 59 Source: http://www.doksinet PRINCIPLES OF MODERN CHEMISTRY, 8E David W. Oxtoby, Pomona College; H Pat Gillis, University of California - Los Angeles; Laurie J. Butler, The University of Chicago Long considered the standard for honors and high-level mainstream general chemistry courses, PRINCIPLES OF MODERN CHEMISTRY continues to set the standard as the most modern, rigorous, and chemically and mathematically accurate text on the market. This authoritative text features an “atoms first” approach and thoroughly revised chapters on Quantum Mechanics and Molecular Structure (Chapter 6), Electrochemistry (Chapter 17), and Molecular Spectroscopy and Photochemistry (Chapter 20). In addition, the text utilizes mathematically accurate and artistic atomic and molecular orbital art, and is student friendly without compromising its rigor. End-of-chapter study aids focus on only the most important key objectives, equations and concepts, making it easier for students

to locate chapter content, while applications to a wide range of disciplines, such as biology, chemical engineering, biochemistry, and medicine deepen students’ understanding of the relevance of chemistry beyond the classroom. NEW TO THIS EDITION • The most powerful online learning solution for chemistry is better than ever. OWLv2 now has more flexible student and instructor functionality, new personalized study tools, enhanced integration with learning management systems, and improved analytics. For this course, OWLv2 also includes Quick Prep, an online short course to 60 review key chemistry concepts and essential skills, new iPad-compatible visualizations, tutorials, and simulations, and new Adaptive Study Plans. In addition, Tutors, Visualizations and Simulations have been converted from Flash to HTML, allowing for easier navigation and streamlined grading. • The most powerful online learning solution for chemistry is better than ever. OWLv2 now has more flexible student

and instructor functionality, new personalized study tools, enhanced integration with learning management systems, and improved analytics. For this course, OWLv2 also includes Quick Prep, an online short course to review key chemistry concepts and essential skills, new iPad-compatible visualizations, tutorials, and simulations, and new Adaptive Study Plans. In addition, Tutors, Visualizations and Simulations have been converted from Flash to HTML, allowing for easier navigation and streamlined grading. • Recognizing that in the top colleges and universities that use this text over 90 percent of students taking introductory chemistry have taken a single variable calculus course in high school, or are taking calculus as a co-requisite for the course, we have improved several portions of the text. These revisions include a more quantitative treatment of the forces and potential energy in molecules, dipole moments, molecular collisions, and the Maxwell-Boltzmann distribution of molecular

speeds. The concepts of slope and area are introduced in the physical and chemical contexts in which they arise, and differential and integral notation is used in parallel with these concepts. Thus, students with a single-variable calculus background are engaged fully, while students without that background will not be at a disadvantage. Simple vectors are introduced to aid in discussing force and velocity, with a new section in Appendix C covering vectors in Cartesian coordinates. FEATURES • OWLv2 is the most trusted online learning solution for chemistry. Featuring chemist-developed content, OWLv2 is the only system designed to elevate thinking through Mastery Learning, www.cengageasiacom Source: http://www.doksinet • • • • • allowing students to work at their own pace until they understand each concept and skill. Each time a student tries a problem, OWLv2 changes the chemicals, values, and sometimes even the wording of the question to ensure students are

learning the concepts and not cheating the system. With detailed, instant feedback and interactive learning resources, students get the help they need when they need it. Now with improved student and instructor tools and greater functionality, OWLv2 is more robust than ever. Discover the power of OWLv2 and take learning to a higher level. AN “ATOMS FIRST” APPROACH places coverage of structure and bonding early in the text (Chapter 4-6), taking students right into the core topics of the course and helping them build a strong conceptual understanding of chemistry. A UNIQUE APPROACH TO LEARNING CHEMICAL PRINCIPLES emphasizes the scientific process from observation to application, placing general chemistry into perspective for serious-minded science and engineering students. MATHEMATICALLY ACCURATE MOLECULAR ORBITAL ART helps students visualize how orbital equations translate into the shapes of the orbitals. A FOCUS ON PROBLEM SOLVING. Problems are grouped into three categories: 1)

Paired problems in the first set are grouped by section, with answers to the odd-numbered paired problems collected in Appendix G so students can check their answer to the first problem in a pair before undertaking the second parallel problem. 2) Additional Problems (unpaired) provide further applications of the principles developed in the chapter. 3) Cumulative Problems integrate material from the chapter with topics presented earlier in the book. More challenging problems are integrated throughout the problem sets and are indicated with asterisks. PEDAGOGICALLY IMPORTANT APPENDICES. Appendix A discusses experimental error and scientific notation; Appendix B introduces the SI system of units used throughout the book, describes the methods used for converting units, and provides a brief review of some fundamental principles in physics. Appendix C provides a review of mathematics for general chemistry, including a new section on vectors in Cartesian coordinates. Appendices D, E, and F

are compilations of thermodynamic, electrochemical, and physical data, respectively. CONTENTS Unit I. Introduction to the Study of Modern Chemistry.1 The Atom in Modern Chemistry2 Chemical Formulas, Equations, and Reaction Yields.Unit II Chemical Bonding and Molecular Structure.3 Atomic Shells and Classical Models of Chemical Bonding.4 Introduction to Quantum Mechanics.5 Quantum Mechanics and Atomic Structure.6 Quantum Mechanics and Molecular Structure.7 Bonding in Organic Molecules8 Bonding in Transition Metal Compounds and Coordination Complexes.Unit III Kinetic Molecular Description of the States of Matter.9 The Gaseous State.10 Solids, Liquids, and Phase Transitions11 Solutions.Unit IV Equilibrium in Chemical Reactions.12 Thermodynamic Processes and Thermochemistry.13 Spontaneous Processes and Thermodynamic Equilibrium.14 Chemical Equilibrium.15 Acid–Base Equilibria16 Solubility and Precipitation Equilibria.17 ElectrochemistryUnit V. Rates of Chemical and Physical Processes18

Chemical Kinetics.19 Nuclear Chemistry20 Molecular Spectroscopy and Photochemistry. Unit VI. Materials21 Structure and Bonding in Solids.22 Inorganic Materials23 Polymeric Materials and Soft Condensed Matter.Appendix A Scientific Notation and Experimental Error.Appendix B. SI Units, Unit Conversions, and Physics for General Chemistry.Appendix C Mathematics for General Chemistry.Appendix D Standard Chemical Thermodynamic Properties.Appendix E Standard Reaction Potentials at 25°C.Appendix F Physical Properties of the Elements.Appendix G Solutions to the Odd-Numbered Problems.Index/Glossary 2016, 1280pp, Hardback, 9781305079113 www.cengageasiacom 61 Source: http://www.doksinet PRINCIPLES OF MODERN CHEMISTRY, HYBRID EDITION (WITH OWLV2 PRINTED ACCESS CARD), 8E David W. Oxtoby, Pomona College; H Pat Gillis, University of California - Los Angeles; Laurie J. Butler, The University of Chicago Long considered the standard for honors and high-level mainstream general chemistry courses,

PRINCIPLES OF MODERN CHEMISTRY continues to set the standard as the most modern, rigorous, and chemically and mathematically accurate text on the market. This authoritative text features an “atoms first” approach and thoroughly revised chapters on Quantum Mechanics and Molecular Structure (Chapter 6), Electrochemistry (Chapter 17), and Molecular Spectroscopy and Photochemistry (Chapter 20). In addition, the text utilizes mathematically accurate and artistic atomic and molecular orbital art, and is student friendly without compromising its rigor. End-of-chapter study aids focus on only the most important key objectives, equations and concepts, making it easier for students to locate chapter content, while applications to a wide range of disciplines, such as biology, chemical engineering, biochemistry, and medicine deepen students’ understanding of the relevance of chemistry beyond the classroom. NEW TO THIS EDITION • The most powerful online learning solution for chemistry is

better than ever. OWLv2 now has more flexible student and instructor functionality, new personalized study tools, enhanced integration with learning management systems, and improved analytics. For this course, OWLv2 62 also includes Quick Prep, an online short course to review key chemistry concepts and essential skills, new iPad-compatible visualizations, tutorials, and simulations, and new Adaptive Study Plans. In addition, Tutors, Visualizations and Simulations have been converted from Flash to HTML, allowing for easier navigation and streamlined grading. • The most powerful online learning solution for chemistry is better than ever. OWLv2 now has more flexible student and instructor functionality, new personalized study tools, enhanced integration with learning management systems, and improved analytics. For this course, OWLv2 also includes Quick Prep, an online short course to review key chemistry concepts and essential skills, new iPad-compatible visualizations, tutorials,

and simulations, and new Adaptive Study Plans. In addition, Tutors, Visualizations and Simulations have been converted from Flash to HTML, allowing for easier navigation and streamlined grading. • Recognizing that in the top colleges and universities that use this text over 90 percent of students taking introductory chemistry have taken a single variable calculus course in high school, or are taking calculus as a co-requisite for the course, we have improved several portions of the text. These revisions include a more quantitative treatment of the forces and potential energy in molecules, dipole moments, molecular collisions, and the Maxwell-Boltzmann distribution of molecular speeds. The concepts of slope and area are introduced in the physical and chemical contexts in which they arise, and differential and integral notation is used in parallel with these concepts. Thus, students with a single-variable calculus background are engaged fully, while students without that background

will not be at a disadvantage. Simple vectors are introduced to aid in discussing force and velocity, with a new section in Appendix C covering vectors in Cartesian coordinates. FEATURES • OWLv2 is the most trusted online learning solution for chemistry. Featuring chemist-developed content, OWLv2 is the only system designed www.cengageasiacom Source: http://www.doksinet • • • • • to elevate thinking through Mastery Learning, allowing students to work at their own pace until they understand each concept and skill. Each time a student tries a problem, OWLv2 changes the, chemistry, values, and sometimes even the wording of the question to ensure students are learning the concepts and not cheating the system. With detailed, instant feedback and interactive learning resources, students get the help they need when they need it. Now with improved student and instructor tools and greater functionality, OWLv2 is more robust than ever. Discover the power of OWLv2 and take

learning to a higher level. AN “ATOMS FIRST” APPROACH places coverage of structure and bonding early in the text (Chapter 4-6), taking students right into the core topics of the course and helping them build a strong conceptual understanding of chemistry. A UNIQUE APPROACH TO LEARNING CHEMICAL PRINCIPLES emphasizes the scientific process from observation to application, placing general chemistry into perspective for serious-minded science and engineering students. MATHEMATICALLY ACCURATE MOLECULAR ORBITAL ART helps students visualize how orbital equations translate into the shapes of the orbitals. A FOCUS ON PROBLEM SOLVING. Problems are grouped into three categories: 1) Paired problems in the first set are grouped by section, with answers to the odd-numbered paired problems collected in Appendix G so students can check their answer to the first problem in a pair before undertaking the second parallel problem. 2) Additional Problems (unpaired) provide further applications of the

principles developed in the chapter. 3) Cumulative Problems integrate material from the chapter with topics presented earlier in the book. More challenging problems are integrated throughout the problem sets and are indicated with asterisks. PEDAGOGICALLY IMPORTANT APPENDICES. Appendix A discusses experimental error and scientific notation; Appendix B introduces the SI system of units used throughout the book, describes the methods used for converting units, and provides a brief review of some fundamental principles in physics. Appendix C provides a review of mathematics for general chemistry, including a new section on vectors in Cartesian coordinates. Appendices D, E, and F are compilations of thermodynamic, electrochemical, and physical data, respectively. CONTENTS Unit I. Introduction to the Study of Modern Chemistry.1 The Atom in Modern Chemistry2 Chemical Formulas, Equations, and Reaction Yields.Unit II Chemical Bonding and Molecular Structure.3 Atomic Shells and Classical

Models of Chemical Bonding.4 Introduction to Quantum Mechanics.5 Quantum Mechanics and Atomic Structure.6 Quantum Mechanics and Molecular Structure.7 Bonding in Organic Molecules8 Bonding in Transition Metal Compounds and Coordination Complexes.Unit III Kinetic Molecular Description of the States of Matter.9 The Gaseous State.10 Solids, Liquids, and Phase Transitions11 Solutions.Unit IV Equilibrium in Chemical Reactions.12 Thermodynamic Processes and Thermochemistry.13 Spontaneous Processes and Thermodynamic Equilibrium.14 Chemical Equilibrium.15 Acid–Base Equilibria16 Solubility and Precipitation Equilibria.17 ElectrochemistryUnit V. Rates of Chemical and Physical Processes18 Chemical Kinetics.19 Nuclear Chemistry20 Molecular Spectroscopy and Photochemistry. Unit VI. Materials21 Structure and Bonding in Solids.22 Inorganic Materials23 Polymeric Materials and Soft Condensed Matter.Appendix A Scientific Notation and Experimental Error.Appendix B. SI Units, Unit Conversions, and

Physics for General Chemistry.Appendix C Mathematics for General Chemistry.Appendix D Standard Chemical Thermodynamic Properties.Appendix E Standard Reaction Potentials at 25°C.Appendix F Physical Properties of the Elements.Appendix G Solutions to the Odd-Numbered Problems.Index/Glossary 2016, 1136pp, Paperback, 9781305395893 www.cengageasiacom 63 Source: http://www.doksinet • • • CHEMISTRY, 5E The Molecular Science John W. Moore, University of Wisconsin, Madison; Conrad L Stanitski, Franklin and Marshall College Authors Moore and Stanitski, both winners of the ACS Pimentel Award in Chemical Education, infuse CHEMISTRY: THE MOLECULAR SCIENCE, Fifth Edition, with timely everyday applications that reveal chemistry as a lively and relevant subject that is fundamental to a broad range of disciplines such as engineering, biology, and environmental science. A revised, annotated art program emphasizes the three concept levels in a pedagogically sound approach to understanding

molecules, concepts, and mathematical equations. Many of the book’s end-of-chapter questions are accompanied by interactive, assignable, online lessons in OWLthe #1 online learning system for chemistry. Engage your students in active study of chemistry with this text. NEW TO THIS EDITION • The first five chapters of the previous edition have been condensed into three chapters. The new Chapter 1 includes material on the metric system, and significant figures (previously in Chapter 2) along with the periodic table coverage previously in Chapters 2 and 3. Chapter 2 now includes the material previously in Chapters 2 and 3. The approach to reactions in aqueous solution has been completely revised and content previous in Chapters 4 and 5 is consolidate into a new Chapter 3. Balancing chemical equations and three reaction types (precipitation; acid-base, and redox) are now discussed before quantitative 64 • • • • • • treatments (reaction stoichiometry, solution

concentrations and solution stoichiometry/ titrations) in Chapter 3. Partly due to consolidating changes cited above, the book has been reduced to 20 chapters instead of 22 previously. Revised all Problem-Solving Examples (PSEs) to a four-step Analyze, Plan, Execute, and Check Result format. Problem-solving strategy is clearly delineated in Chapter 1 where students are provided a study strategy for problem solving examples. Each CO photo has an associated caption that raises chemistry-based questions that are then answered within the chapter. Specific chapter sections are noted with the questions. Made much greater use of annotations (“balloons”) that are incorporated into award-winning illustrations; this pedagogically sound practice reduces the need for running text, helps shorten the book, and helps students learn better. The variety, comprehensiveness, and conceptual level of chapter-end Questions for Review and Thought (QRTs) have been expanded. There are many new chapter-end

Questions for Review and Thought (QRTs). Aligned QRTs for each chapter with the end-ofchapter summary Having Studied objectives based on Bloom’s Taxonomy of Learning Objectives. Assessed each QRT based on Bloom’s Taxonomy to insure adequate numbers of questions for each taxonomic category. New QRTs written to insure meeting this number. Summary Problems at the end of each chapter help students learn and integrate chapter concepts and provide good study aids for exams. Many Summary Problems are entirely new and all have been edited and improved. CONTENTS 1. The Nature of Chemistry 2 Chemical Compounds.3 Chemical Reactions4 Energy and Reactions.5 Electron Configurations and the Periodic Table.6 Covalent Bonding7 Molecular Structures.8 Properties of Gases9 Liquids, Solids, and Materials.10 Fuels, Organic Chemicals, and Polymers.11 Chemical Kinetics: www.cengageasiacom Source: http://www.doksinet Rates of Reactions12. Chemical Equilibrium13 The Chemistry of Solutes and

Solutions.14 Acids and Bases.15 Additional Aqueous Equilibria.16 Thermodynamics: Directionality of Chemical Reactions.17 Electrochemistry and Its Applications.18 Nuclear Chemistry19 The Chemistry of the Main Group Elements.20 Chemistry of Selected Transition Elements and Coordination Compounds.Appendix A: Problem Solving and Mathematical Operations.Appendix B: Units, Equivalences, and Conversion Factors. Appendix C: Physical Constants and Sources of Data.Appendix D: Ground-State Electron Configurations of Atoms.Appendix E: Naming Simple Organic Compounds.Appendix F: Ionization Constants for Weak Acids at 25°C.Appendix G: Ionization Constants for Weak Bases at 25°C. Appendix H: Solubility Product Constants for Some Inorganic Compounds at 25°C.Appendix I: Standard Reduction. Potentials in Aqueous Solution at 25 °C.Appendix J: Selected Thermodynamic Values Appendix K: Answers to Problem-Solving Practice Problems.Appendix L: Answers to Exercises Appendix M: Answers to Selected

Questions for Review and Thought. 2015, 1264pp, Hardback, 9781285199047 CHEMISTRY, 5E The Molecular Science, Hybrid Edition (with OWLv2 24-Months Printed Access Card) John W. Moore, University of Wisconsin, Madison; Conrad L Stanitski, Franklin and Marshall College Reflecting Cengage Learning’s commitment to offering flexible teaching solutions and value for students and instructors, this new hybrid version features the instructional presentation found in the printed text while delivering all the end-of chapter exercises online in OWLv2, the leading online learning system for chemistry. The result--a briefer printed text that engages students online! Help your students improve their grades and understanding of concepts with this value-packed Hybrid Edition. An access code to OWLv2 with MindTap Reader, is included with the text, providing students with powerful online resources that include tutorials, simulations, randomized homework questions, videos, a complete interactive

electronic version of the textbook, and more! Your students will be engaged in the active study of chemistry with CHEMISTRY: THE MOLECULAR SCIENCE, Fifth Edition. Authors Moore and Stanitski, both winners of the ACS Pimentel Award in Chemical Education, infuse their text with timely everyday applications that reveal chemistry as a lively and relevant subject that is fundamental to a broad range of disciplines such as engineering, biology, and environmental science. A revised, annotated art program emphasizes the three concept levels in a pedagogically sound approach to understanding molecules, concepts, and mathematical equations. Many of the book’s end-of-chapter questions are accompanied by interactive, assignable, online www.cengageasiacom 65 Source: http://www.doksinet lessons in OWLv2--the #1 online learning system for chemistry. NEW TO THIS EDITION • The first five chapters of the previous edition have been condensed into three chapters. The new Chapter 1 includes

material on the metric system, and significant figures (previously in Chapter 2) along with the periodic table coverage previously in Chapters 2 and 3. Chapter 2 now includes the material previously in Chapters 2 and 3. The approach to reactions in aqueous solution has been completely revised and content previous in Chapters 4 and 5 is consolidate into a new Chapter 3. Balancing chemical equations and three reaction types (precipitation; acid-base, and redox) are now discussed before quantitative treatments (reaction stoichiometry, solution concentrations and solution stoichiometry/ titrations) in Chapter 3. • Partly due to consolidating changes cited above, the book has been reduced to 20 chapters instead of 22 previously. • Revised all Problem-Solving Examples (PSEs) to a four-step Analyze, Plan, Execute, and Check Result format. Problem-solving strategy is clearly delineated in Chapter 1 where students are provided a study strategy for problem solving examples. • Each CO photo

has an associated caption that raises chemistry-based questions that are then answered within the chapter. Specific chapter sections are noted with the questions. • Made much greater use of annotations (“balloons”) that are incorporated into award-winning illustrations; this pedagogically sound practice reduces the need for running text, helps shorten the book, and helps students learn better. • The variety, comprehensiveness, and conceptual level of chapter-end Questions for Review and Thought (QRTs) have been expanded. • There are many new chapter-end Questions For Review and Thought (QRTs). • Aligned QRTs for each chapter with the end-ofchapter summary Having Studied objectives based on Bloom’s Taxonomy of Learning Objectives. • Assessed each QRT based on Bloom’s Taxonomy 66 to insure adequate numbers of questions for each taxonomic category. New QRTs written to insure meeting this number. • Summary Problems at the end of each chapter help students learn and

integrate chapter concepts and provide good study aids for exams. Many Summary Problems are entirely new and all have been edited and improved. CONTENTS 1. The Nature of Chemistry 2 Chemical Compounds.3 Chemical Reactions4 Energy and Reactions.5 Electron Configurations and the Periodic Table.6 Covalent Bonding7 Molecular Structures.8 Properties of Gases9 Liquids, Solids, and Materials.10 Fuels, Organic Chemicals, and Polymers.11 Chemical Kinetics: Rates of Reactions12. Chemical Equilibrium13 The Chemistry of Solutes and Solutions.14 Acids and Bases.15 Additional Aqueous Equilibria.16 Thermodynamics: Directionality of Chemical Reactions.17 Electrochemistry and Its Applications.18 Nuclear Chemistry19 The Chemistry of the Main Group Elements.20 Chemistry of Selected Transition Elements and Coordination Compounds.Appendix A: Problem Solving and Mathematical Operations.Appendix B: Units, Equivalences, and Conversion Factors.Appendix C: Physical Constants and Sources of Data.Appendix D:

Ground-State Electron Configurations of Atoms. Appendix E: Naming Simple Organic Compounds. Appendix F: Ionization Constants for Weak Acids at 25 °C,Appendix G: Ionization Constants for Weak Bases at 25°CAppendix H: Solubility Product Constants for Some Inorganic Compounds at 25°C. Appendix I : Standard Reduction. Potentials in Aqueous Solution at 25°C.Appendix J: Selected Thermodynamic Values.Appendix K: Answers to Problem-Solving Practice Problems.Appendix L: Answers to Exercises.Appendix M: Answers to Selected Questions for Review and Thought. 2015, 1056pp, Paperback, 9781285461847 www.cengageasiacom Source: http://www.doksinet key media components. NEW TO THIS EDITION CHEMISTRY & CHEMICAL REACTIVITY, HYBRID EDITION (WITH OWLV2 24-MONTHS PRINTED ACCESS CARD), 9E John C. Kotz, State University of New York, Oneonta; Paul M Treichel, University of Wisconsin, Madison; John Townsend, West Chester University of Pennsylvania; David Treichel, Nebraska Wesleyan University

Reflecting Cengage Learning’s commitment to offering flexible teaching solutions and value for students and instructors, this new hybrid version features the instructional presentation found in the printed text while delivering all the end-of chapter exercises online in OWLv2, the leading online learning system for chemistry. The result--a briefer printed text that engages students online! Help your students improve their grades and understanding of concepts with this value-packed Hybrid Edition. An access code to OWLv2 with MindTap Reader, is included with the text, providing students with powerful online resources that include tutorials, simulations, randomized homework questions, videos, a complete interactive electronic version of the textbook, and more! Help your students succeed in chemistry with the clear explanations, problem-solving strategies, and dynamic study tools of CHEMISTRY & CHEMICAL REACTIVITY, 9th edition. Combining thorough instruction with the powerful

multimedia tools you need to develop a deeper understanding of general chemistry concepts, the text emphasizes the visual nature of chemistry, illustrating the close interrelationship of the macroscopic, symbolic, and particulate levels of chemistry. The art program illustrates each of these levels in engaging detail--and is fully integrated with • The five topical interchapters in previous editions have been integrated into standard chapters: Milestones in the Development of Chemistry and the Modern World View of Atoms and Molecules has been folded into Chapter 2. The Chemistry of Fuels and Energy Resources and The Chemistry of the Environment have been incorporated into an expanded new chapter on Environmental Chemistry (Chapter 20). The Chemistry of Life: Biochemistry has been expanded into a full chapter (Chapter 24). The Chemistry of Modern Materials has been incorporated into the chapter on solids (Chapter 12). • Chapter Goals (and Chapter Goals Revisited) have been recast

into three categories that most express what students should get out of the course: 1. Understand: chapter concepts 2. Do: Be able to carry out calculations, draw molecular structures, make chemical decisions. 3. Remember: important facts and chemical concepts. • Access to the #1 online homework and learning system for chemistry, OWLv2, is packaged with this text. Now with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader™, a new eBook with apps and embedded video, audio, annotations, and activities. OWLv2 courses for Gen Chem, GOB, and Liberal Arts now include Quick Prep essential skills assignments that can be taken before the semester

begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text and new iPad-compatible visualizations, tutorials, and simulations. FEATURES • WORKED EXAMPLES. Through the text’s six-part www.cengageasiacom 67 Source: http://www.doksinet • • • • • 68 worked example structure, students learn how to approach a problem rather than to memorize problem types and solution approaches. Worked example headers use the following structure: 1) A Problem statement; 2) A “What Do You Know?” section that asks students to outline what information they have and begin to think about a solution; 3) A Strategy section that combines the information available with the objective to devise a path to the solution; 4) A fully worked Solution; 5) A “Think About Your Answer” section that prompts students to ask if the answer is reasonable; 6) A “Check Your

Understanding” problem similar to the example to confirm students understand. PROBLEM STRATEGY MAPS. Selected worked examples have Strategy Maps that give students a visual view of the complete problem-solving strategy. Video Strategy Solutions based on these maps are integrated into the MindTap eBook. REVIEW & CHECK PROBLEMS. These sectionending problems help students hone their skill in assessing whether they understand the concepts in the section. VISUAL TOOLS. With the text’s extensive use of molecular representations, your students can move beyond plugging numbers into an equation to a true understanding of what’s going on at the molecular level. The authors consistently depict molecules in chemical equations and use unique space-filling molecular art that more completely ties the text’s molecular art to problem solving and media. CASE STUDY BOXES. Cases show students where chemistry has been used to solve a problem or where chemistry is important in everyday matters.

Examples include the use of isotopes to catch athletes who cheat using illegal drugs, a washing machine that injects silver into the wash, acrylamide in French fries, a comparison of ethanol and gasoline, and the amount of salt in seawater. Questions posed in each Case Study are answered in an appendix. “IN THE LABORATORY” QUESTIONS. These questions in OWLv2 address techniques used and work performed in the general chemistry laboratory to help students make the connection between lecture topics and lab work. • BEYOND THE EXAM. The text correlates Chapter Goals with Study Questions to help students develop a conceptual understanding of chemistry and a skill in problem-solving that will serve them long after their final exams. CONTENTS PART I: CONCEPTS OF CHEMISTRY.1 Basic Concepts of Chemistry.Let’s Review: The Tools of Quantitative Chemistry.2 Atoms, Molecules, and Ions.3 Chemical Reactions4 Stoichiometry: Quantitative Information from Chemical Reactions.5 Principles of

Chemical Reactivity: Energy and Chemical Reactions.PART II: ATOMS AND MOLECULES.6 The Structure of Atoms7 The Structure of Atoms and Periodic Trends.8 Covalent Bonding and Molecular Structure.9 Bonding and Molecular Structure - Valence Bond and Molecular Orbital Theory.Part 3: States of Matter10 Gases and Their Properties.11 Intermolecular Forces and Liquids.12 Ionic Bonding, Metals, and the Solid State.13 Solutions and Their BehaviorPART IV: THE CONTROL OF CHEMICAL REACTIONS.14 Chemical Kinetics - The Rates of Chemical Reactions.15 Principles of Reactivity: Chemical Equilibria.16 Equlibria and Acids and Bases17 Principles of Reactivity: Other Aspects of Aqueous Equilibria.18 Thermodynamics - Entropy and Free Energy.19 Principles of Reactivity: Electron Transfer Reactions.PART V: THE CHEMISTRY OF THE ELEMENTS.20 Environmental Chemistry: Earth’s Environment, Energy, and Sustainability.21 The Chemistry of the Main Group Elements.22 The Chemistry of the Transition Elements.23 Carbon:

Not Just Another Element.24 Biochemistry25 Nuclear Chemistry.Appendix A: Using Logarithms and the Quadratic Equation.Appendix B: Some Important Physical Concepts.Appendix C: Abbreviations and Useful Conversion Factors.Appendix D: Physical Constants.Appendix E: Naming Organic Compounds.Appendix F: Values for the Ionization Energies and Electron Affinities of the Elements. Appendix G: Vapor Pressure of Water at Various Temperatures.Appendix H: Ionization Constants for Weak Acids at 25ºC.Appendix I: Ionization Constants for Weak Bases at 25ºC.Appendix J: Solubility Product Constants for Some Inorganic Compounds at 25ºC.Appendix K: Formation www.cengageasiacom Source: http://www.doksinet Constants for Some Complex Ions in Aqueous Solution.Appendix L: Selected Thermodynamic Values.Appendix M: Standard Reduction Potentials in Aqueous Solution at 25ºC.Appendix N: Answers to Chapter Opening and Case Study Questions, Check Your Understanding Questions, Review and Check Questions 2015,

1152pp, Paperback, 9781285462530 and post-laboratory exercises and concluding thought-provoking questions--helps to enhance students’ conceptual understanding. NEW TO THIS EDITION • Labs have been updated with the most recent data and values in order to accurately reflect the changes in lab courses. • The new Activity 35 adds additional challenges and experiments, and Activity 36 provides exercises that develop graphing skills. FEATURES EXPERIMENTS IN GENERAL CHEMISTRY, 6E Steven L. Murov, Modesto Junior College EXPERIMENTS IN GENERAL CHEMISTRY, Sixth Edition, has been designed to stimulate curiosity and insight, and to clearly connect lecture and laboratory concepts and techniques. To accomplish this goal, an extensive effort has been made to develop experiments that maximize a discoveryoriented approach and minimize personal hazards and ecological impact. Like earlier editions, the use of chromates, barium, lead, mercury, and nickel salts has been avoided. The absence of

these hazardous substances should minimize disposal problems and costs. This lab manual focuses not only on what happens during chemical reactions, but also helps students understand why chemical reactions occur. The sequence of experiments has been refined to follow topics covered in most general chemistry textbooks. In addition, Murov has included a correlation chart that links the experiments in the manual to the corresponding chapter topics in several Cengage Learning general chemistry titles. Each experiment--framed by pre- • Murov focuses not only on what happens during chemical reactions but also helps students understand “why” chemical reactions occur. • Each experiment includes pre-laboratory exercises and thought-provoking questions (with answers to selected questions). • Review Exercises, found at the end of the manual, help students test their understanding of key concepts and synthesize the material they have learned. • A number of experiments include

post-laboratory exercises and conclude with a set of review exercises. • A procedure for following the visual clock reaction spectroscopically, instead of visually, is included in the kinetics experiment. This also provides a link between the equilibrium and kinetics experiments. • As with the previous editions, the use of chromates, barium, lead, mercury, and nickel salts has been avoided, effectively minimizing disposal problems and decreasing costs. • A correlation chart links the experiments to corresponding chapter topics in several Cengage Learning general chemistry titles, including Kotz, Masterton, Moore, and Whitten. • An Online Instructor’s Manual contains resources designed to streamline and maximize the effectiveness of course preparation. It includes a list of chemicals and quantities required for each experiment per student and solutions to Pre-Lab problems. CONTENTS Preface, Correlation table and Chemistry Resources SAFETY FIRST1. Early Explorations

www.cengageasiacom 69 Source: http://www.doksinet and Terminology.2 Separation of Mixtures3 Measurements and Identification Techniques.4 Density, Accuracy, Precision and Graphing.5 Empirical Formulas.6 Classification of Chemical Reactions.7 Quantitative Precipitation8 Electrical Conductivity and Electrolytes.9 Ionic Reactions10 Activities of Metals.11 Quantitative Solution Chemistry.12 Thermochemistry13 Properties of Elements and Compounds: An Internet Study.14 Spectroscopy of Cobalt (II) Ion.15 Lewis Structures and Molecular Models.16 Molecular Polarity and Chromatography.17 Gas Law Studies18 Cooling Curves and Crystal Structures.19 Water Purification and Analysis.20 Organic Models and Isomerism21 Acids and Bases: Reactions and Standardization.22 Acids and Bases: Analysis.23 Acids and Bases: pH, pKa Measurements.24 Equilibrium - Solubility Product.25 Equilibrium - Determination of Keq.26 Complexes27 Rates and Mechanisms of Reactions - Visual and/or Spectroscopic Monitoring.28

Synthesis of Copper (II) Glycinate29 Standardization of Thiosulfate.30 Analysis of Bleach and Copper (II) Glycinate.31 Redox Reactions32 Electrochemistry.33 Spectroscopic Analysis of Aspirin.34 Polymer Properties and Selections35 Additional Challenges and Experiments36. Graphing Quantitative RelationshipsAppendix 1: Properties of SubstancesAppendix 2: Common Ions by ChargeAppendix 3: Solubilities of Ionic CompoundsAppendix 4: Solutions to Starred Prelaboratory Problems 2015, 464pp, Paperback, 9781285458540 CHEMISTRY, 9E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Susan A. Zumdahl, University of Illinois, Urbana-Champaign This fully updated Ninth Edition of Steven and Susan Zumdahl’s CHEMISTRY brings together the solid pedagogy, easy-to-use media, and interactive exercises that today’s instructors need for their general chemistry course. Rather than focusing on rote memorization, CHEMISTRY uses a thoughtful approach built on problem-solving. For the Ninth

Edition, the authors have added a new emphasis on critical systematic problem solving, new critical thinking questions, and new computerbased interactive examples to help students learn how to approach and solve chemical problems--to learn to think like chemists--so that they can apply the process of problem solving to all aspects of their lives. Students are provided with the tools to become critical thinkers: to ask questions, to apply rules and develop models, and to evaluate the outcome. In addition, Steven and Susan Zumdahl crafted ChemWork, an online program included in OWL Online Web Learning to support their approach, much as an instructor would offer support during office hours. ChemWork is just one of many study aids available with CHEMISTRY that supports the hallmarks of the textbook--a strong emphasis on models, real world applications, visual learning, and independent problem solving. Available with InfoTrac® Student Collections http://gocengage. com/infotrac. NEW TO THIS

EDITION • A NEW EMPHASIS ON SYSTEMATIC PROBLEM SOLVING now appears in the applications of 70 www.cengageasiacom Source: http://www.doksinet dimensional analysis. • NEW CRITICAL THINKING QUESTIONS have been added throughout the text to emphasize the importance of conceptual learning. • NEW COMPUTER-BASED INTERACTIVE EXAMPLES force students to think through the example step-by-step rather than simply scan the written example in the text as many students do. New Interactive Examples are available in OWL Online Web Learning. In addition, key examples from the text have been made into Interactive Tutorial problems and are available to assign in the OWL program. • NEW CHEMWORK PROBLEMS have been added to the end-of-chapter problems throughout the text to test students’ understanding of core concepts. They can be worked as pencil-andpaper problems or in interactive form in OWL, where students who solve a problem with no assistance can proceed directly to the answer and students

who need help can get assistance through a series of hints. The hints in OWL-usually in the form of interactive questions that guide students through the problem-solving process--are modeled after the way an instructor would assist a student with homework problems during office hours. Students cannot derive the answer in OWL through pattern recognition; rather, they are encouraged to continue working though the hints to arrive at the answer. • NEW END-OF–CHAPTER QUESTIONS AND PROBLEMS have been added throughout the text. • THE REVISED AND UPDATED ART PROGRAM has been modified as needed, and new macro/ micro illustrations have been added. • A NEW SECTION ON LIMITING REACTANTS in Chapter 3, the treatment of stoichiometry, emphasizes calculating the amounts of products that can be obtained from each reactant. Students are taught how to select a limiting reactant both by comparing the amounts of reactants present and by calculating the amounts of products that can be formed by

complete consumption of each reactant. • A NEW SECTION ON PHOTOELECTRON SPECTROSCOPY was added to Chapter 9 (Section 9.6) • ENHANCED OWL (ONLINE WEB LEARNING) INTEGRATION: For the Ninth Edition, OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes Student Self- Assessments, ChemWork problems, Interactive Examples from the text, the interactive customizable Cengage YouBook, a customizable iPad-compatible multimedia eBook, and an optional Solutions Manual eBook. FEATURES • PROBLEM-SOLVING STRATEGY BOXES focus the student’s attention on the very important process of problem solving, helping them learn to think like chemists. CONTENTS 1. Chemical Foundations2 Atoms, Molecules, and Ions.3 Stoichiometry4 Types of Chemical Reactions and Solution Stoichiometry.5 Gases6

Thermochemistry.7 Atomic Structure and Periodicity.8 Bonding: General Concepts9 Covalent Bonding: Orbitals.10 Liquids and Solids.11 Properties of Solutions12 Chemical Kinetics.13 Chemical Equilibrium14 Acids and Bases.15 Acid-Base Equilibria16 Solubility and Complex Ion Equilibria.17 Spontaneity, Entropy, and Free Energy.18 Electrochemistry19 The Nucleus: A Chemist’s View.20 The Representative Elements.21 Transition Metals and Coordination Chemistry.22 Organic and Biological Molecules Appendix 1. Mathematical ProceduresA11 Exponential Notation.A12 LogarithmsA13 Graphing Functions.A14 Solving Quadratic Equations.A15 Uncertainties in Measurements Appendix 2. The Quantitative Kinetic Molecular Model.Appendix 3 Spectral AnalysisAppendix 4. Selected Thermodynamic DataAppendix 5 Equilibrium Constants and Reduction Potentials. A5.1 Values of Ka for Some Common Monoprotic Acids.A52 Stepwise Dissociation Constants for Several Common Polyprotic Acids.A53 Values of Kb for Some Common Weak

Bases.A54 Ksp Values at 25 C for Common Ionic Solids.A55 Standard Reduction Potentials at 25 C (298K) www.cengageasiacom 71 Source: http://www.doksinet for Many Common Half-Reactions.Appendix 6 SI Units and Conversion Factors.GlossaryAnswers to Selected Exercises. 2014, 1200pp, Hardback, 9781133611097 CHEMISTRY, HYBRID EDITION (WITH OWLV2 24-MONTHS PRINTED ACCESS CARD), 10E Kenneth W. Whitten, University of Georgia; Raymond E Davis, University of Texas, Austin; Larry Peck, Texas A&M University; George G. Stanley, Louisiana State University Reflecting Cengage Learning’s commitment to offering flexible teaching solutions and value for students and instructors, this new hybrid version features the instructional presentation found in the printed text while delivering all the end-of chapter exercises online in OWL, the leading online learning system for chemistry. The resulta briefer printed text that engages students online! This new Hybrid edition of CHEMISTRY continues to

incorporate a strong molecular reasoning focus, amplified problem-solving exercises, a wide range of reallife examples and applications, and innovative technological resources. With this text’s focus on molecular reasoning, your students will learn to think at the molecular level and make connections between molecular structure and macroscopic properties. The Tenth Edition has been revised throughout and now includes a reorganization of the descriptive chemistry chapters to improve the flow of topics, a new basic math skills Appendix, an updated art program with new “talking labels” that fully explain what is going on in the figure, and 72 much more. NEW TO THIS EDITION • REORGANIZATION OF DESCRIPTIVE CHEMISTRY CHAPTERS (22-28): To facilitate an improved flow of the descriptive chemistry topics optionally covered in many courses and to provide more convenient options for custom versions of the textbook, Chapters 22 through 28 have been reorganized as follows: Chapter 22 is

now Nuclear Chemistry; Chapter 23, Organic Chemistry I: Formulas, Names and Properties; Chapter 24, Organic Chemistry II: Shapes, Selected Reactions, and Biopolymers; Chapter 25, Coordination Compounds; Chapter 26, Metals I: Metallurgy; Chapter 27, Metals II: Properties and Reactions; and Chapter 28, Some Nonmetals and Metalloids. • NEW BASIC MATH SKILLS APPENDIX: To aid the flow of introductory chemistry material in Chapter 1, a review of topics in basic mathematics skills, including scientific notation and use of significant figures, with numerous Examples, now appears in Appendix A. Related Exercises remain in the Measurements and Calculations area at the end of Chapter 1. • REORGANIZED INTRODUCTION TO AQUEOUS SOLUTIONS: Section 6-1 has been reorganized to improve the descriptive introduction to aspects of aqueous solutions, including ionization and dissociation, acids, bases, and solubility guidelines. These basic ideas are then elaborated in the classification of reactions in

the remainder of Chapter 6 and serve as a foundation throughout the textbook for further discussion of physical and chemical properties of solutions. • MORE COMPREHENSIVE COVERAGE OF CENTRAL ATOM LONE PAIRS: In Chapter 8, a more comprehensive tabular summary of the influence of central atom lone pairs on molecular geometry has been added to enhance student understanding. • A REVISED AND UPDATED ART PROGRAM: The Tenth Edition’s art program has been revised to include “talking labels” placed strategically within figures to explain what is going on in the illustration, so students can focus on learning instead of trying to figure out what is going on by www.cengageasiacom Source: http://www.doksinet going back and forth between a caption and the art. To exemplify the beauty and excitement of chemistry, the individual layouts of many figures have been revised to be more visually pleasing, balanced, and organized. The art program now includes more molecular models generated by

the latest software to enhance the molecular reasoning theme. All electrostatic charge potential (ECP) art includes a more thorough explanation of its use. • ENHANCED OWL ONLINE WEB LEARNING: For the Tenth Edition, OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes MindTap Reader. MindTap Reader is a free upgrade to existing readers in Cengage’s existing digital platforms offering significant new functionality while also preparing the platforms to take advantage of future MindTap services. FEATURES • MOLECULAR REASONING AND VISUALIZATION EMPHASIS: Molecular reasoning is woven throughout the text in chapter objectives, chapter essays, examples, and end-of-chapter problems and highlighted by a molecular reasoning icon. • CHAPTER-OPENING APPLICATIONS AND “CHEMISTRY IN USE”

BOXES: These built-in learning aids illustrate the practical applications of chemistry in such areas as the environment, the development of science, research and technology, and our daily lives. • “BEYOND THE TEXTBOOK” QUESTIONS: These end-of-chapter questions ask students to solve problems through the use of online exercises in OWL, as well as other materials. • “STOP & THINK” BOXES: Throughout the text, these boxes alert students to common mistakes and points of emphasis in problem solving. Some Types of Chemical Reactions.7 Chemical Bonding.8 Molecular Structure and Covalent Bonding Theories.9 Molecular Orbitals in Chemical Bonding.10 Reactions in Aqueous Solutions I: Acids, Bases, and Salts.11 Reactions in Aqueous Solutions II: Calculations.12 Gases and the Kinetic-Molecular Theory.13 Liquids and Solids14 Solutions.15 Chemical Thermodynamics16 Chemical Kinetics.17 Chemical Equilibrium18 Ionic Equilibria I: Acids and Bases.19 Ionic Equilibria II: Buffers and

Titration Curves.20 Ionic Equilibria III: The Solubility Product Principle.21 Electrochemistry.22 Nuclear Chemistry23 Organic Chemistry I: Formulas, Names and Properties.24 Organic Chemistry II: Shapes, selected Reactions, and Biopolymers.25 Coordination Compounds26 Metals I: Metallurgy.27 Metals II: Properties and Reactions.28 Some Nonmetals and Metalloids Appendix A: Basic Math Skills (includes new significant figure section).Appendix B: Electron Configurations of the Atoms of the Elements. Appendix C: Common Units, Equivalences, and Conversion Factors.Appendix D: Physical Constants.Appendix E: Some Physical Constants for a Few Common Substances.Appendix F: Ionization Constants for Weak Acids at 25°C. Appendix G: Ionization Constants for Weak Bases at 25°C.Appendix H: Solubility Product Constants for Some Inorganic Compounds at 25°C.Appendix I: Dissociation Constants for Some Complex Ions. Appendix J: Standard Reduction Potentials in Aqueous Solution at 25°C.Appendix K: Selected

Thermodynamic Values at 298.15 KAppendix L: Answers to Selected Even-Numbered Numerical Exercises.Index of EquationsGlossary/Index 2014, 1008pp, Paperback, 9781285186054 CONTENTS 1. The Foundations of Chemistry2 Chemical Formulas and Composition Stoichiometry.3 Chemical Equations and Reaction Stoichiometry.4 The Structure of Atoms.5 Chemical Periodicity6 www.cengageasiacom 73 Source: http://www.doksinet study aids available with CHEMISTRY that supports the hallmarks of the textbooka strong emphasis on models, real world applications, visual learning, and independent problem solving. NEW TO THIS EDITION CHEMISTRY, HYBRID EDITION (WITH OWLV2 24-MONTHS PRINTED ACCESS CARD), 9E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Susan A. Zumdahl, University of Illinois, Urbana-Champaign Reflecting Cengage Learning’s commitment to offering flexible teaching solutions and value for students and instructors, this new hybrid version features the instructional presentation

found in the printed text while delivering all the end-of chapter exercises online in OWL, the leading online learning system for chemistry. The resulta briefer printed text that engages students online! This fully updated Hybrid Edition of Steven and Susan Zumdahl’s CHEMISTRY 9e brings together the solid pedagogy, easy-to-use media, and interactive exercises that today’s instructors need for their general chemistry course. Rather than focusing on rote memorization, CHEMISTRY uses a thoughtful approach built on problem-solving. For the Ninth Edition, the authors have added a new emphasis on critical systematic problem solving, new critical thinking questions, and new computer-based interactive examples to help students learn how to approach and solve chemical problemsto learn to think like chemistsso that they can apply the process of problem solving to all aspects of their lives. Students are provided with the tools to become critical thinkers: to ask questions, to apply rules and

develop models, and to evaluate the outcome. In addition, Steven and Susan Zumdahl crafted ChemWork, an online program included in OWL Online Web Learning to support their approach, much as an instructor would offer support during office hours. ChemWork is just one of many 74 • A NEW EMPHASIS ON SYSTEMATIC PROBLEM SOLVING now appears in the applications of dimensional analysis. • NEW CRITICAL THINKING QUESTIONS have been added throughout the text to emphasize the importance of conceptual learning. • NEW COMPUTER-BASED INTERACTIVE EXAMPLES force students to think through the example step-by-step rather than simply scan the written example in the text as many students do. New Interactive Examples are available in OWL Online Web Learning. In addition, key examples from the text have been made into Interactive Tutorial problems and are available to assign in the OWL program. • NEW CHEMWORK PROBLEMS have been added to the end-of-chapter problems throughout the text to test

students’ understanding of core concepts. They can be worked as pencil-andpaper problems or in interactive form in OWL, where students who solve a problem with no assistance can proceed directly to the answer and students who need help can get assistance through a series of hints. The hints in OWL-usually in the form of interactive questions that guide students through the problem-solving process--are modeled after the way an instructor would assist a student with homework problems during office hours. Students cannot derive the answer in OWL through pattern recognition; rather, they are encouraged to continue working though the hints to arrive at the answer. • NEW END-OF–CHAPTER QUESTIONS AND PROBLEMS have been added throughout the text. • THE REVISED AND UPDATED ART PROGRAM has been modified as needed, and new macro/ micro illustrations have been added. • A NEW SECTION ON LIMITING REACTANTS in Chapter 3, the treatment of stoichiometry, emphasizes calculating the amounts of

products that can be obtained from each reactant. Students are taught how to select a limiting reactant both by www.cengageasiacom Source: http://www.doksinet comparing the amounts of reactants present and by calculating the amounts of products that can be formed by complete consumption of each reactant. • A NEW SECTION ON PHOTOELECTRON SPECTROSCOPY was added to Chapter 9 (Section 9.6) • ENHANCED OWL (ONLINE WEB LEARNING) INTEGRATION: For the Ninth Edition, OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes Student Self- Assessments, ChemWork problems, and Interactive Examples from the text. OWL also includes MindTap Reader MindTap Reader is a free upgrade to existing readers in Cengage’s existing digital platforms offering significant new functionality while also preparing

the platforms to take advantage of future MindTap services. Model.Appendix 3 Spectral AnalysisAppendix 4. Selected Thermodynamic DataAppendix 5 Equilibrium Constants and Reduction Potentials. A5.1 Values of Ka for Some Common Monoprotic Acids.A52 Stepwise Dissociation Constants for Several Common Polyprotic Acids.A53 Values of Kb for Some Common Weak Bases.A54 Ksp Values at 25 C for Common Ionic Solids.A55 Standard Reduction Potentials at 25 C (298K) for Many Common Half-Reactions.Appendix 6 SI Units and Conversion Factors.GlossaryAnswers to Selected Exercises. 2014, 944pp, Paperback, 9781285188492 FEATURES • PROBLEM-SOLVING STRATEGY BOXES focus the student’s attention on the very important process of problem solving, helping them learn to think like chemists. CONTENTS 1. Chemical Foundations2 Atoms, Molecules, and Ions.3 Stoichiometry4 Types of Chemical Reactions and Solution Stoichiometry.5 Gases6 Thermochemistry.7 Atomic Structure and Periodicity.8 Bonding: General Concepts9

Covalent Bonding: Orbitals.10 Liquids and Solids.11 Properties of Solutions12 Chemical Kinetics.13 Chemical Equilibrium14 Acids and Bases.15 Acid-Base Equilibria16 Solubility and Complex Ion Equilibria.17 Spontaneity, Entropy, and Free Energy.18 Electrochemistry19 The Nucleus: A Chemist’s View.20 The Representative Elements.21 Transition Metals and Coordination Chemistry.22 Organic and Biological Molecules Appendix 1. Mathematical ProceduresA11 Exponential Notation.A12 LogarithmsA13 Graphing Functions.A14 Solving Quadratic Equations.A15 Uncertainties in Measurements Appendix 2. The Quantitative Kinetic Molecular EXPERIMENTS IN GENERAL CHEMISTRY: INQUIRY AND SKILL BUILDING, 2E Vickie Williamson, Texas A&M University; Larry Peck, Texas A&M University With many years of teaching experience in the classroom and laboratory, Vickie Williamson and Larry Peck have created EXPERIMENTS IN GENERAL CHEMISTRY: INQUIRY AND SKILL BUILDING, 2nd edition with carefully crafted and tested

experiments designed to complement any general chemistry curriculum. The authors have selected three types of lab experiments to meet all of the needs of students and instructors looking for a selection of laboratory pedagogy. There are Skill Building experiments to develop techniques and demonstrate previously developed concepts, Guided Inquiry experiments to direct the students to collect data on variables without previously studying www.cengageasiacom 75 Source: http://www.doksinet the concepts and guide them to look for patterns in the data, and Open Inquiry experiments to allow the students to apply concepts or relationships in a new setting. Twenty-eight experiments feature Pre-Lab questions and Post-Lab questions on perforated pages for easy removal of worksheets, and there is a Common Procedures and Concepts section as an appendix for easy retrieval of basic information for students. NEW TO THIS EDITION • Updated experiments throughout with 2 brand new experiments added

to this edition. FEATURES • Two-semester safety agreements. • Perforated pages allow for easy removal of worksheets. • Thirty total experiments (2 completely new) featuring Skill Building experiments, Guided Inquiry experiments and Open Inquiry experiments, meet all of the needs of students and instructors looking for a selection of laboratory pedagogy. • Common Procedures and Concepts section allows for easy retrieval of basic information for students. CONTENTS EXPERIMENT 1 - Are Labels Accurate or Precise? (An Open Inquiry Experiment).EXPERIMENT 2 Density Measurements (A Skill Building Experiment) EXPERIMENT 3 - Cost of a Chemical Product(A Guided Inquiry Experiment).EXPERIMENT 4 - Soap Making (A Skill Building Experiment).EXPERIMENT 5 - Reactions of Calcium(A Guided Inquiry Experiment).EXPERIMENT 6 - Aluminum and Copper (II) Chloride(A Guided Inquiry Experiment). EXPERIMENT 7 (was 6) - Recycling Aluminum Cans (A Skill Building Experiment).EXPERIMENT 8 - Patterns(A Guided

Inquiry Experiment). EXPERIMENT 9 (was 7) - Solutions and Crystals of Alum (A Guided Inquiry Experiment).EXPERIMENT 10 (was 8) - Analysis of a Carbonated Beverage(A Guided Inquiry Experiment).EXPERIMENT 11 (was 9) - Mass Relationships in Reactions(An Open Inquiry Experiment).EXPERIMENT 12 (was 10) - Shapes of Molecules and Ions(A Guided Inquiry Experiment). EXPERIMENT 13 (was 11) - The Fuel in a Bic® Lighter(A Guided Inquiry Experiment).EXPERIMENT 76 14 (was 12) - Alka-Seltzer®: An Application of Gas Laws(A Guided Inquiry Experiment).EXPERIMENT 15 (was 13) - Freezing Points of Solutions(A Guided Inquiry Experiment).EXPERIMENT 16 (was 14) - Spectrochemical Analysis(A Guided Inquiry Experiment).EXPERIMENT 17 (was 15) - Heat of Crystallization(A Skill Building Experiment).EXPERIMENT 18 (was 16) - Enthalpy of Reaction (A Guided Inquiry Experiment). EXPERIMENT 19 (was 17) - The Kinetics of the Decomposition of Hydrogen Peroxide(A Guided Inquiry Experiment).EXPERIMENT 20 (was 18) -

Kinetics of Decoloration of Crystal Violet(A Guided Inquiry Experiment).EXPERIMENT 21 (was 19) - Factors Affecting Reactions(A Guided Inquiry Experiment).EXPERIMENT 22 (was 20) - Formation of a Complex(A Skill Building Experiment).EXPERIMENT 23 (was 21) - Acids and pH(A Guided Inquiry Experiment).EXPERIMENT 24 (was 22) - Reactions of Acids And Bases(A Guided Inquiry Experiment).EXPERIMENT 25 (was 23) - Acids and Bases(An Open Inquiry Experiment). EXPERIMENT 26 (was 24) - Electrochemistry(A Guided Inquiry Experiment).EXPERIMENT 27 (was 25) - Small-Scale Redox Titration(A Skill Building Experiment).EXPERIMENT 28 (was 26) - The Copper Cycle(A Open Inquiry Experiment). EXPERIMENT 29 (was 27) - Organic Molecules(A Guided Inquiry Experiment).EXPERIMENT 30 (was 28) - Reactions of Organic Compounds(A Guided Inquiry Experiment).Common Procedures and Concepts. 2014, 412pp, Paperback, 9781285433172 www.cengageasiacom Source: http://www.doksinet EXPERIMENTS IN GENERAL CHEMISTRY, LAB MANUAL,

10E LAB MANUAL FOR ZUMDAHL/ ZUMDAHL’S CHEMISTRY, 9TH, 9E Rupert Wentworth, Indiana University; Barbara H. Munk Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Susan A. Zumdahl, University of Illinois, Urbana-Champaign Build skill and confidence in the lab with the 61 experiments included in this manual. Safety is strongly emphasized throughout the lab manual. 2014, 624pp, Paperback, 9781133611486 Each experiment in this manual was selected to match topics in the textbook and includes an introduction, a procedure, a page of pre-lab exercises about the concepts the lab illustrates, and a report form. Some have a scenario that places the experiment in a real-world context. In addition, each experiment has a link to a set of references and helpful online resources. 2013, 512pp, Paperback, 9781111989422 www.cengageasiacom 77 Source: http://www.doksinet acknowledges that good science must remain utterly open to revision. • Over one hundred practical, relevant

exercises and examples address common conceptual issues and pitfalls confronted in students’ own practices of scientific learning. • Real-life examples from scientific literature provide immediate practical applications of the concepts encountered in the book. CONTENTS A BEGINNER’S GUIDE TO SCIENTIFIC METHOD, INTERNATIONAL EDITION, 4E Stephen S. Carey, Portland Community College This concise yet comprehensive guide provides an introduction to the scientific method of inquiry as well as detailed coverage of the many misapplications of scientific method that define pseudoscience. Compact enough to be used as a supplementary book in a science class, yet thorough enough in its coverage to be used as a core text in a class on scientific method, this text assists students in using the scientific method to design and assess experiments. NEW TO THIS EDITION • The explanations have been thoroughly to ensure clarity and readability for the student audience. • The discussion of

causation in Chapter 3 has been greatly expanded. • In Chapter 4, the basic framework for discussing experimental design has been revised to center on false confirmation and rejection. • In Chapter 5, the discussion of probability and statistical inference is greatly simplified. Each section now begins with and explains all points in terms of recent causal studies. • Two new pseudoscientific fallacies have been added and the text now contains many new and recent illustrations of all the fallacies. • Dozens of new exercises and examples have been added to every chapter. • End of chapter concept quizzes have been added. Preface.1 SCIENCE Just What is Science? Asking Why. Scientific Method The Consequences of Science. Scientific Method in Daily Life Things to Come. Exercises2 OBSERVATION Making Accurate Observations. Anomalous Phenomena Observing Anomalies. The Burden of Proof Concept Quiz. Exercises3 EXPLANATION Explanation, Theory and Hypothesis. Causation Correlation Causal

Mechanisms. Underlying Processes Laws Function. The Interdependence of Explanatory Methods. Rival Explanations and Ockham’s Razor Explanation and Description. Ultimate Explanations Concept Quiz. Exercises4 EXPERIMENTATION The Basic Method. Confirmation and Rejection Designing a Good Test. Real World Experiments How Not to Design a Test. Conceptual Vagueness Testing Extraordinary Claims. Predictive Clarity Bias and Expectation. Concept Quiz Exercises5 ESTABLISHING CAUSAL LINKS. Causal Studies Ruling Out Chance. Multiple Causal Factors Randomized, Prospective and Retrospective Studies. Reading Between the Lines Concept Quiz. Exercises6 FALLACIES IN THE NAME OF SCIENCE. What is a Fallacy? False Anomalies Questionable Arguments by Elimination. Illicit Causal Inferences. Unsupported Analogies and Similarities Untestable Explanations and Predictions. Empty Jargon. Ad Hoc Rescues Exploiting Uncertainty Science and Pseudoscience. Concept Quiz Exercises.FURTHER READINGINDEX 2012, 160pp,

Paperback, 9781111726010 FEATURES • An introduction to the scientific method which 78 www.cengageasiacom Source: http://www.doksinet • CHEMISTRY An Atoms First Approach, International Edition Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Susan A. Zumdahl, University of Illinois, Urbana-Champaign Steve and Susan Zumdahl’s texts focus on helping students build critical thinking skills through the process of becoming independent problem-solvers. They help students learn to “think like a chemists” so they can apply the problem solving process to all aspects of their lives. In CHEMISTRY: AN ATOMS FIRST APPROACH, 1e, International Edition the Zumdahls use a meaningful approach that begins with the atom and proceeds through the concept of molecules, structure, and bonding, to more complex materials and their properties. Because this approach differs from what most students have experienced in high school courses, it encourages them to focus on conceptual

learning early in the course, rather than relying on memorization and a “plug and chug” method of problem solving that even the best students can fall back on when confronted with familiar material. The atoms first organization provides an opportunity for students to use the tools of critical thinkers: to ask questions, to apply rules and models and to • • FEATURES • AN ATOMS FIRST APPROACH. By taking an atoms first approach, the authors are able to provide students with a unified story built around an organizing principle – start the course with smallest element, the atom, and build from there. Building their explanations around this structure, the authors consistently show the importance and relevance of studying chemistry. • A FOCUS ON CONCEPTUAL UNDERSTANDING. • Rather than focusing on memorizing, the book gives students the tools they need to become critical thinkers: to ask questions, to apply rules and develop models, and to evaluate the outcome. A LOGICAL

ORGANIZATION. Chapter 1 provides an introduction to the key components of the storythe atom, atomic structure, energy, and the mole. Chapter 2 initiates the plan of going from the simple to the complex. Chapter 3 covers counting by weighing, atomic masses, the mole, and introduces chemical equations. Chapter 4 covers the fundamental ideas of bonding to explain how atoms are tied together. Chapter 5 covers detailed models of bonding and structure: Chapter 6 covers chemical energy; Chapters 7 and 8 cover gases, liquids, and solids, and Chapter 9 covers stoichiometry. A STRONG PROBLEM-SOLVING ORIENTATION. Throughout the text, problem-solving strategies help students learn to solve problems by thinking them through rather than brute-force memorizing. Section 6.2 “Learning to Solve Problems” emphasizes the importance of thoughtful, creative problem solving, demonstrating that thinking through a problem produces more long-term, meaningful learning that can be applied to “real life”

than memorizing steps that apply only to a particular type of problem. The problem-solving process is organized in terms of “Where are we going?’; “How do we get there?” and “Reality Check,” which prompts students to check whether their answer makes sense. STUDENT-ORIENTED LEARNING AIDS. Problem-solving strategy boxes help students focus on particular aspects of problem-solving; concept summary boxes help students organize their thinking about crucial concepts; and chemical connections boxes present applications of chemistry in various fields and in daily life. INTERACTIVE EXAMPLES encourage students to think their way through the example instead of passively reading through the solution. Electronic versions of select examples are assignable in OWL. Students can work these Interactive Examples multiple times to help them master the problem-solving process, receiving slightly different examples each time they attempt an www.cengageasiacom 79 Source: http://www.doksinet

Interactive Example. • END-OF-CHAPTER VISUAL EXERCISES, called out with an icon, provide students with opportunities to demonstrate a conceptual understanding of fundamental chemical principles. Many take an “atomic view” of matter to help students appreciate the usefulness of the atomic model in understanding macroscopic properties. Other problems ask students to interpret graphs or to explain figures. • A FOCUS ON THE FUNDAMENTAL IDEAS OF CHEMISTRY. Numerous discussions, illustrations, and exercises are designed to help students overcome misconceptions by providing a more accurate picture of the fundamental ideas of chemistry. The book emphasizes the importance of developing a qualitative understanding of concepts before approaching quantitative problems. • AN OUTSTANDING ART PROGRAM. The book represents the microscopic world of chemistry to give students a picture in their minds of “what the atoms and molecules are doing” through an excellent art program and

animations. • END-OF-CHAPTER ACTIVE LEARNING QUESTIONS. Because students often learn the most when they teach each other, these questions are intended for group discussion. CONTENTS Review Chapter: Measurement and Calculations in Chemistry.1 Chemical Foundations 2 Atomic Structure and Periodicity.3 Atoms to Molecules4 Bonding: General Concepts.5 Molecular Structure and Orbitals.6 Chemical Energy7 Gases8 Liquids and Solids.9 Stoichiometry10 Types of Chemical Reactions and Solution Stoichiometry.11 Properties of Solutions.12 Chemical Kinetics13 Chemical Equilibrium.14 Acids and Bases15 Acid-Base Equilibria.16 Solubility and Complex Ion Equilibria.17 Spontaneity, Entropy, and Free Energy.18 Electrochemistry19 The Nucleus: A Chemist’s View.20 The Representative Elements.21 Transition Metals and coordination Chemistry.22 Organic and Biological Molecules Appendix 1: SI Units and Conversion Factors. Appendix 2: Mathematical Procedures. Appendix 3: The Quantitative Kinetic Molecular Model.

80 Appendix 4: Spectral Analysis. Appendix 5: Selected Thermodynamic Data. Appendix 6: Equilibrium Constants and Reduction Potentials. 2012, 1152pp, Paperback, 9780840065865 CHEMISTRY, 7E Principles and Reactions William L. Masterton, University of Connecticut, Emeritus; Cecile N. Hurley, University of Connecticut; Edward Neth, University of Connecticut Masterton/Hurley/Neth’s CHEMISTRY: PRINCIPLES AND REACTIONS, 7e, takes students directly to the crux of chemistry’s fundamental concepts and allows you to efficiently cover all topics found in the typical general chemistry book. Based on the authors’ extensive teaching experience, this updated edition includes new concept-driven, rigorous examples, updated examples that focus on molecular reasoning and understanding, and “Chemistry: Beyond the Classroom” essays that demonstrate the relevance of the concepts and highlight some of the most upto-date uses of chemistry. A strong, enhanced art program assists students in

visualizing chemical concepts. Integrated end-of-chapter questions and Key Concepts correlate to OWL Online Learning, the #1 online homework and tutorial system for chemistry. OWL also includes an interactive eBook for the 7th edition of the textbook and an optional ebook for the Student Study Guide. NEW TO THIS EDITION • REORGANIZATION: The authors have reorganized Chapters 13, 15, and 19 to create a better flow from single to multiple equilibria. In www.cengageasiacom Source: http://www.doksinet • • • • • addition, Chapters 2-5 have been reorganized to enhance student understanding and mirror the way this material is presented in the classroom. NEW CHAPTER 15: This new chapter covers complex ion and precipitation equilibria to enhance the book’s coverage. NEW END-OF-CHAPTER PROBLEMS/ QUESTIONS: Approximately 25% of the book’s end- of-chapter problems and questions are new. REVISED VISUALS FOR BETTER CLARITY: Ensure your students’ understanding of concepts as

this edition moves relevant text from captions to talking labels within the art for a clearer presentation of visual images. Contemporary photographs, modern molecular models, and new concept flow charts help further clarify key concepts. NEW AND INNOVATIVE EXAMPLE FORMAT-ONE/TWO COLUMN COMBO: Revised examples provide rigorous practice and opportunities to apply concepts. Each Example begins with a problem statement followed by three problemsolving steps: 1) Analysis (two columns), 2) Strategy (one column), and 3) Solution (two column). This innovative new worked Example format presentation is clear, consistent, and easy to follow. Each example concludes with an End Point, which provides additional insight into the problem. REVISED GRADED AND CONCEPTUAL EXAMPLES: Revised in-text Graded Examples now show the gradual increase in difficulty as problems progress from Step “a” to Step “c.” The Graded Examples simulate the presentation of problems on a test. Additional Conceptual

Examples lead students through conceptualizing the chemistry principles just discussed and demonstrate how to refine thinking skills at critical points in the chapter. FEATURES the latest research in “Chemistry: Beyond the Classroom” boxes. Students see the relevance of concepts in some of the most current work in chemistry, including photochromic and thermochromic materials, coloration biological organisms, molecular structure of rubbery materials, and fuel cells. • STRONG COVERAGE OF ORGANIC CHEMISTRY: Students leave your course well equipped with organic chemistry skills through coverage of nomenclature and a greater number of functional groups, as well as coverage of types of organic reactions and material on proteins and carbohydrates. • MOLECULAR MODEL ART PROGRAM: Effective models visually reinforce students’ conceptual understanding. Revised nanoscale views of atoms, molecules, and ions use molecular modeling software and an exacting threedimensional style to offer

effective visual learning tools throughout the text. CONTENTS 1. Matter and Measurements2 Atoms, Molecules, and Ions.3 Mass Relations in Chemistry; Stoichiometry.4 Reactions in Aqueous Solution5 Gases.6 Electronic Structure and the Periodic Table.7 Covalent Bonding8 Thermochemistry9 Liquids and Solids.10 Solutions11 Rate of Reaction.12 Gaseous Chemical Equilibrium13 Acids and Bases.14 Equilibria in Acid-Base Solutions.15 Complex ion and Precipitation Equilibria16. Spontaneity of Reaction17 Electrochemistry.18 Nuclear Reactions19 Complex Ions and Coordination compounds20. Chemistry of the Metals.21 Chemistry of the Nonmetals.22 Organic Chemistry23 Organic Polymers, Natural and Synthetic. 2012, 800pp, Hardback, 9781111427108 • CONNECTION TO FINE ARTS: This edition connects the hard science of chemistry to the humanities and fine arts through chapter openers and literary quotations that enhance each chapter’s content. • LATEST WORK FROM SPECIALISTS: Guest authors and leaders in

specialized fields profile www.cengageasiacom 81 Source: http://www.doksinet CHEMISTRY, 3E Principles and Practice, International Edition Daniel L. Reger, University of South Carolina; Scott R Goode, University of South Carolina; David W. Ball, Cleveland State University A text that truly embodies its name, CHEMISTRY: PRINCIPLES AND PRACTICE, 3rd, International Edition connects the chemistry students learn in the classroom (principles) with real-world uses of chemistry (practice). The authors accomplish this by starting each chapter with an application drawn from a chemical field of interest and revisiting that application throughout the chapter. The Case Studies, Practice of Chemistry essays, and Ethics in Chemistry questions reinforce the connection of chemistry topics to areas such as forensics, organic chemistry, biochemistry, and industry. NEW TO THIS EDITION • Each chapter begins with an opening application drawn from a chemical field of interest, which is revisited

throughout the chapter. • Worked Examples include problem flow diagrams that map out the problem-solving process in a graphical manner, aiding students in developing problem-solving thought processes and strategies. Many examples use color to aid students in showing how the initial data in the problem is transformed through the various steps of the problem to the answer. • Case Studies are multi-pronged, multi-step problems that examine real world uses of chemistry. Summary Problems focus on a problem of chemical interest and draw on material from the entire chapter for their solutions. • Ethics in Chemistry questions, located at the 82 end of each chapter before the problem sets, emphasize the human side of chemistry and remind students that chemistry is not just a set of facts. These questions discuss the ethical issues and dilemmas scientists face in practicing their profession. They also are good exercises for schools that have a writing-across-the-curriculum requirement.

• This edition fully integrates OWL (Online Webbased Learning), the homework management system trusted by tens of thousands of students. • Integrated end-of-chapter questions correlate to OWL. An optional e-book of this edition is also available in OWL. In addition, Go Chemistry™ learning modules developed by award-winning chemists offer mini-lectures and learning tools that play on video iPods, personal video players, QuickTime, Windows Media Player, and iTunes. (iPods, iTunes, iPhone are products of Apple, Inc.) FEATURES • This book presents chemistry concepts in an experimental context by demonstrating how the facts and theories have come from many years of experimentation. This is emphasized in the text with margin icons. • Each section begins with a set of Learning Objectives and ends with an Objectives Review. The exercises also are grouped by objectives. • Principles of Chemistry essays expand and/or reinforce important topics discussed in the book. Practice of

Chemistry essays are real-world applications of chemistry; i.e, why and how chemists and other professionals use chemistry in their jobs and daily lives. • The text includes approximately 2000 Questions and Exercises. Questions are qualitative in nature, often conceptual, and include problem-solving skills. Questions that are suitable for a brief writing exercise are designated with the symbol of a pencil. The more-challenging items are designated with a triangle. The text also has end-of-chapter exercises available for use in OWL, Brooks/ Cole’s online homework and assessment system. Exercises are paired, with the odd-numbered ones having answers in the appendix and a similar evennumbered problem immediately following. While most exercises appear in the order in which they www.cengageasiacom Source: http://www.doksinet are discussed, there are also Chapter Exercises that are uncategorized, and Cumulative Exercises that integrate concepts and methods introduced in earlier

chapters. Cumulative Exercises often contain multiple parts and/or multiple steps. CONTENTS 1. Introduction to Chemistry2 Atoms, Molecules, and Ions.3 Equations, the Mole, and Chemical Formulas.5 Chemical Reactions in Solution Thermochemistry.6 The Gaseous State7 Electronic Structure.8 The Periodic Table: Structure and Trends.9 Chemical Bonds10 Molecular Structure and Bonding Theories.11 Liquids and Solids12 Solutions.13 Chemical Kinetics14 Chemical Equilibrium.15 Solutions of Acids and Bases16 Reactions Between Acids and Bases.17 Chemical Thermodynamics.18 Electrochemistry19 Metals, Coordination Chemistry, and Metallurgy.20 The Chemistry of Hydrogen, Elements in Groups 3A through 6A, and the Noble Gases.21 Nuclear Chemistry.22 Organic Chemistry and Biochemistry Appendix A: Math Procedures.Appendix B: Selected Physical Constants.Appendix C: Unit Conversion Factors.Appendix D: Names of IonsAppendix E: Properties of Water.Appendix F: Solubility Products, Acids, and Bases.Appendix G:

Thermodynamic Constants for Selected Compounds.Appendix H: Standard Reduction Potentials at 25.Appendix I: Glossary.Appendix J: Answers to Selected Exercises. 2010, 1120pp, Paperback, 9780495559832 EXPERIMENTS IN GENERAL CHEMISTRY, 2E Featuring MeasureNet Bobby Stanton, University of Georgia; Lin Zhu, University of Georgia; Charles “Butch” Atwood, University of Georgia Innovative and self-directed, EXPERIMENTS IN GENERAL CHEMISTRYFEATURING MEASURENET, 2nd Edition prepares students for the laboratory setting by asking them multicomponent questions, building their knowledge from previous experiments, and incorporating the innovative MeasureNet network data collection system into the manual. MeasureNet improves the laboratory experience by requiring smaller amounts of chemicals for experimentsmaking the lab safer and more environmentally friendlyand greatly increasing precision through its electronic data collection, analysis, and reduction features. NEW TO THIS EDITION • Convey

the most relevant ideas with the most current experiments. All 28 experiments in the manual have been revised for this edition. • Help students develop their own experiments with 6 new experiments in the more challenging selfdirected format. Students use their knowledge, skills, and techniques from prior concept/ technique-oriented experiments to solve an assigned problem. • Encourage strong laboratory fundamentals with 22 guided inquiry experiments, which lead students through an experiment by asking a series of questions. • Heighten interest in chemistry and its real-world applications with four all-new, self-directed experiments: “Quality Control for GlassEx Window www.cengageasiacom 83 Source: http://www.doksinet Cleaner,” “Determining the Iron Content in Cereal,” “Analyzing the Chemical Content of Chromite,” and “Determining the Time Interval Between Doses of a Cardiac Drug.” • Reinforce important concepts with new pre- and post-lab questions for all

self-guided experiments. Students will also appreciate the new easier-touse format and lab reports for these experiments. FEATURES • Focus students’ efforts with experiments that require less time collecting data and encourage more time analyzing and manipulating it for a better, more useful grasp of chemistry. • Stimulate learning on a deeper level. Students will express their ideas and conclusions in formal writings that help them better comprehend the concepts, techniques, and theories in the manual. • Run an environmentally friendly lab! With MeasureNet, experiments are more precise and require smaller quantities of chemicals, making the lab safer for students and better for the planet. and Bases.22 Dystan Medical Supply Company Cold Packs and Hot Packs.23 KineticsReaction Orders.24 Chemical Equilibria25 Determining the Equilibrium Constant for a Reaction.26 Determining Ka of an Acid by Titration and from pH.27 pH and Buffer Solutions.28 Self-DirectedIdentifying an Unknown

Weak Acid.29 Quality Control for GlassEx Window Cleaner.30 Determining the Iron Content in Cereal.31 Analyzing the Chemical Content of Chromite.32 Determining the Time Interval Between Doses of a Cardiac Drug.33 What is in This Container? 2010, 448pp, Paperback, 9780495561798 CONTENTS Safety Rules.Common Laboratory Glassware and Equipment.1 Densities of Some Liquids and Solids.2 Specific Heat of Substances3 Chromatography.4 Determination of the Percent by Mass of the Components in a Mixture by Thermal Gravimetric Analysis.5 Self DirectedThermal Insulating Materials.6 Reaction Stoichiometry7 Types of Chemical Reactions.8 Identifying Metal Ions and Inorganic Compounds by their Chemical Interactions.9 Gravimetric Analysis of a Chloride, Sulfate, or Carbonate Compound.10 Emission Analysis of Aqueous Solutions of Group IA and IIA Metal Salts.11 Determination of Chromium (VI) Concentrations via Absorption Spectroscopy.12 Determination of the Concentration of Acetic Acid in Vinegar.13

Solubility, Polarity, Electrolytes, and Nonelectrolytes.14 Self-DirectedDetermination of the Cause of a Fish-Kill in the Clark Fork of the Columbia River.15 Self-DirectedQuality Control for the Athenium Baking Soda Company.16 Gas Laws.17 Colligative Properties18 Soaps and Detergents.19 Heats of Chemical and Physical Processes.20 Hess’s Law21 Determination of the Heat of Neutralization of a Variety of Strong Acids 84 LABORATORY INQUIRY IN CHEMISTRY, 3E Richard Bauer, Arizona State University; James Birk, Arizona State University; Doug Sawyer, Scottsdale Community College LABORATORY INQUIRY IN CHEMISTRY, Thrid Edition provides a unique set of guided-inquiry investigations that focus on constructing knowledge about the conceptual basis of laboratory techniques, instead of simply learning techniques. By focusing on developing skills for designing experiments, solving problems, thinking critically, and selecting and applying appropriate techniques, the authors expose students to a

realistic laboratory experience, typical of the practicing chemist. This new edition continues the proven three-phase learning cycle: exploration of chemical behaviors within the context of the problems posed; concept invention--the use of data and observations to construct accepted scientific knowledge about the concepts explored in the laboratory investigation; and, concept www.cengageasiacom Source: http://www.doksinet application--where students apply their conceptual understanding of the investigation at hand by modifying or extending the experiments, and write a report that emphasizes conceptual relevance. These college and honors level inquiry-based experiments correlate well with the recommended experiments outlined by the Advanced Placement Chemistry Development Committee. NEW TO THIS EDITION • The following new experiments have been added to this editon:5. What Relationships Exist Among Elements?11. How Much Acetic Acid Is in Vinegar?24. Why Do Liquids Evaporate at

Different Rates?In addition, new photos have been added throughout to better demonstrate lab instruments, procedures and techniques. FEATURES • Proven three-phase learning cycle: exploration of chemical behaviors within the context of the problems posed; concept invention--the use of data and observations to construct accepted scientific knowledge about the concepts explored in the laboratory investigation; and concept application--where students apply their conceptual understanding of the investigation at hand by modifying or extending the experiments, and write a report that emphasizes conceptual relevance. CONTENTS The Investigations.1 What Are the Safety Concerns in the Laboratory?2. Whats in the Flask?3 How Should Data Trends Be Presented?4. How Is Lab Equipment Used?5. What Relationships Exist Among Elements?6. What’s in the Bottles?7 How Can the Waste Be Made Useful?8. Is the Water Hard or Soft?9. How Hot Is the Water?10 Which Metal Will Burn the Skin?11. How Much Acetic

Acid Is in Vinegar?12. Are All Neutralization Reactions the Same?13. How Many Waters of Hydration Are in the Formula?14. How Much Sodium Bicarbonate Is in the Mixture?15. Is It Economical to Recycle Aluminum?16. What Is a Copper Cycle?17 Who Wrote the Ransom Note?18. How Can UV Sensitive Beads Be Used to Test Sunscreens?19. What Factors Affect the Intensity of Color?20. How Much Cobalt Is in the Soil?21. How Much Copper Is in the Coin?22. Which Iron Compound Is It?23 Should We Mine This Ore?24. Why Do Liquids Evaporate at Different Rates?25. What Are the Structures of Some Alloys?26. How Is LED Light Color Related to Composition?27. What Is the Molar Mass of Mars Ice Gas?28. How Much Gas Is Produced?29 Which Alcohols Are in the Barrels?30. How Is Heat of Combustion Measured Indirectly?31. What Is the Rate Law?32. How Fast Does the Crystal Violet Decolorize?33. Why Is the Vinegar Factory Rusting?34. What Factors Affect the Solubility of Kidney Stones?35. How Many Chemicals Are in the

Vial?36. What Factors Affect Chemical Equilibrium?37. What Is the Formation Constant?38 Are Household Items Acidic, Basic, or Neutral?39. What Is the pH of Soil?40. What Is the Acid Dissociation Constant?41. What Is the Solubility Product?42. What Are Some Chemical Properties of Cream of Tartar?43. What Are the Metals?44 How Can a Battery Be Made from Coins?45. What Is the Complex Ion?46. What Formulation Makes the Best Toy?47. How Are Anions Identified?48 How Are Cations Identified?49. How Are More Cations Identified?50. How Are Ionic Solids Identified?Appendix A: Automated Data Collection. Appendix B: Transmittance and Absorbance Data Collection.Appendix C: Measuring pHAppendix D: Temperature Data Collection.Appendix E: Pressure Data Collection.Appendix F: Voltage Data Collection.Appendix G: Selected Laboratory Techniques.Appendix H: Laboratory Equipment Appendix I: Sample Material Safety Data Sheet. Appendix J: Tables 2009, 288pp, Paperback, 9780495113454 www.cengageasiacom 85

Source: http://www.doksinet INORGANIC CHEMISTRY SURVIVAL GUIDE FOR GENERAL CHEMISTRY WITH MATH REVIEW, 2E Charles H. Atwood, University of Georgia Available for packaging with any CENGAGE textbook, this survival guide focuses on helping students practice for exams by showing them how to solve difficult problems by dissecting them into manageable chunks. The guide includes three levels of proficiency questions – A, B, and minimal – to quickly build student confidence as they master the knowledge needed to succeed in the course. This book is also available for students to purchase separately at www.CENGAGEbraincom CONTENTS Module 1: Metric System, Dimensional Analysis, Significant Figures, and Density.Module 2: Understanding Chemical Formulas.Module 3: Chemical Nomenclature.Module 4: The Mole Concept.Module 5: Chemical Reaction Stoichiometry Module 6: Types of Chemical Reactions.Module 7: Electronic Structure of Atoms.Module 8: Chemical Periodicity.Module 9: Chemical BondingModule

10: Molecular Shapes.Module 11: Hybridization and Polarity of Molecules.Module 12: Acids and Bases.Module 13: States of MatterModule 14: Solutions.Module 15: Heat Transfer, Calorimetry, and Thermodynamics.Module 16: Chemical Kinetics.Module 17: Gas Phase EquilibriaModule 18: Aqueous Equilibria.Module 19: Electrochemistry Module 20: Nuclear Chemistry.Math Review 2008, 216pp, Paperback, 9780495387510 86 DESCRIPTIVE INORGANIC, COORDINATION, AND SOLID STATE CHEMISTRY, 3E Glen E. Rodgers, Allegheny College This proven, sophomore-level text introduces the basics of coordination, solid-state, and descriptive main-group chemistry in a uniquely accessible manner, featuring a “less is more” approach. This approach allows you to present concepts and applications that you find particularly important and fascinating. Consistent with the “less is more” philosophy, the book does not review topics covered in introductory courses, but rather moves directly into topics central to inorganic

chemistry. Written in a conversational prose style that is enjoyable and easy to understand, this book presents not only the basic theories and methods of inorganic chemistry (in three self-standing sections), but also a great deal of the history and applications of the discipline. The new edition features new art, more diversified applications, and a new icon system. And to better help students understand how the seemingly disparate topics of the periodical table connect, the book offers revised coverage of the author’s “Network of Interconnected Ideas” on new full color endpapers, as well as on a convenient tear-out card. The author’s presentation does not assume prerequisites of organic or physical chemistry. NEW TO THIS EDITION • INCREASED EMPHASIS ON THE “NETWORK OF INTERCONNECTED IDEAS.” To better help students understand how the seemingly disparate topics of the periodical table connect, the book www.cengageasiacom Source: http://www.doksinet offers revised

coverage of the author’s “Network of Interconnected Ideas” including a new icon system, full color endpapers, and a convenient tear-out card. • REVISED VISUALS. The text’s art program has been revised for more clarity, and a new icon system makes the Network of Interconnected Ideas art better connect. • UPDATED APPLICATIONS. The applications in Chapter 6 have been updated and diversified, and now cover more transition metals. In addition, the applications in the survey of periodic table groups chapters (12-19) have been updated. • REORDERED APPENDIXES. The book’s appendix have been reorganized to make them easier to use. FEATURES • SELF-CONTAINED SECTIONS. Coordination, solid state, and descriptive inorganic chemistry are presented in self-contained sections. The reader can begin in any one of these sections without becoming frustrated at references to material already learned. These self-standing chapters also allow instructors the flexibility to present material in

any order. • A FOCUS ON UNDERSTANDING THE PERIODIC TABLE. The author systematically builds a network of interconnected ideas to develop reader confidence and to forge an understanding of the periodic table. • “THOUGHT” QUESTIONS. These questions, embedded within the body of the text, encourage students to construct and organize ideas, thought patterns, and concepts, and to go beyond merely memorizing groups of facts or trends. Students must “think” their way through the material. • A FOCUS ON PROBLEM SOLVING. Approximately 1,000 problems challenge students to apply what they have learned to new situations and aid in building a deeper understanding of the material. In addition, a significant number of problems require short explanatory paragraphs, emphasizing the importance of writing in the discipline of chemistry. • A HISTORICAL PERSPECTIVE. A historical perspective is integrated throughout the text to give students an increased appreciation of the centuries of human

endeavor that have led to our present understanding of the chemical world around us. • A WIDE RANGE OF APPLICATIONS show students the practical uses of inorganic chemistry through the discussion of such diverse subjects as heavy metal poisoning and antidotes, nuclear fusion, battery technology, fluoridation, radon as a carcinogen, and automobile air bags. CONTENTS 1. The Evolving Realm of Inorganic Chemistry PART 1: COORDINATION CHEMISTRY.2 An Introduction to Coordination Chemistry.3 Structures of Coordination Compounds.4 Bonding Theories for Coordination Compounds.5 Rates and Mechanisms of Reactions of Coordination Compounds.6 Applications of Coordination Compounds. PART 2: SOLID-STATE CHEMISTRY.7 SolidState Structures8 Solid-State Energetics PART 3: DESCRIPTIVE CHEMISTRY OF THE REPRESENTATIVE ELEMENTS.9 Building a Network of Ideas to Make Sense of the Periodic Table.10 Hydrogen and Hydrides11 Oxygen, Aqueous Solutions, and the Acid-Base Character of Oxides and Hydroxides.12 Group

1A: The Alkali Metals.13 Group 2A: The Alkaline-Earth Metals14 The Group 3A Elements.15 The Group 4A Elements.16 Group 5A: The Pnicogens17 Sulfur, Selenium, Tellurium, and Polonium.18 Group 7A: The Halogens.19 Group 8A: The Noble Gases 2012, 656pp, Hardback, 9780840068460 www.cengageasiacom 87 Source: http://www.doksinet INTRODUCTORY / PREPARATORY CHEMISTRY INTRODUCTORY CHEMISTRY, HYBRID EDITION (WITH OWLV2 PRINTED ACCESS CARD), 6E Mark S. Cracolice, University of Montana; Ed Peters Reflecting Cengage Learning’s commitment to offering flexible teaching solutions and value for students and instructors, this hybrid version of INTRODUCTORY CHEMISTRY, 6e features the instructional presentation found in the printed text while delivering all the end-of chapter exercises online in OWLv2. Access to OWLv2 is included with every new hybrid text, giving your students an interactive learning experience with the convenience of a text that is both brief and affordable. To provide maximum

teaching flexibility and make it easy for you to teach chapters in the order you prefer, the authors include necessary preview or review information with each topic’s coverage. Even more flexibility is provided in the new edition by the included MindTap Reader, an electronic version of the text that features interactivity, integrated media, and additional algebra coverage. Known for its question-and-answer presentation that allows students to actively learn chemistry while studying an assignment, this edition integrates new features such as outstanding technological resources, coached problems in a two-column format, and enhanced art and photography, all of which dovetail with the authors’ active learning approach. NEW TO THIS EDITION 88 • A new Mindtap Reader Version combines multimedia activities, examples, and assessments in an interactive, fully online version of the book that further engages students’ active learning of chemistry, with clickable answer buttons for Active

Examples and pop-up key terms and chapter-inreview material at point of use. • New content includes updated general stoichiometry patterns in Chapters 7, 10, 14 and 16, more in-depth coverage of nomenclature in Chapter 6, and expanded explanations of formulas and names for ionic compounds. • New end-of-chapter “Frequently Asked Questions” anticipate students’ questions on the chapter’s most challenging concepts and problems. Each question includes an answer from the author, with tips for remembering key concepts or solving key problems. • A new “Quick Quiz” feature in the Everyday Chemistry boxes asks students to think critically about the featured topic. (Answers are provided in the Instructor’s Manual.) • A new Key Terms List now appears at the end of each chapter and is clickable in MindTap Reader. • OWLv2, the most powerful online learning solution for chemistry now has more flexible student and instructor functionality, new personalized study tools,

enhanced integration with learning management systems, and improved analytics. OWLv2 now includes ALL quantitative end-ofchapter questions from the book, as well as Quick Prep, an online short course that reviews key chemistry concepts and essential skills; new iPad-compatible visualizations, tutorials, and simulations; and new Adaptive Study Plans with multiple-choice questions that expand upon the book’s Test Yourself questions. In addition, Tutors, Visualizations and Simulations have been converted from Flash to HTML, allowing for easier navigation and streamlined grading. FEATURES • Active Examples: Teaching core chemical skills, these two-column examples allow students to first actively work through and complete steps in the right column, and then see the answer to each step in the left column, thereby receiving immediate feedback about their understanding of www.cengageasiacom Source: http://www.doksinet the concept as it is being formed. The first frame is labeled

“Think Before You Write” and encourages students to slow down and analyze the problem statement before working on the solution. Each example is titled so that students can better identify the concept or problem-solving skill they are learning and can easily locate specific concepts to review when preparing for exams. • Chapter Summaries: This section at the back of the book includes summaries of each chapter’s goals and key concepts, as well as chapterspecific self-tests and answers for extra practice. • Flexible Format: The book has been structured so that any common sequence of topics is supported, allowing you to present topics in any order you prefer. • P/Review Cross-References: A supplement to the optional order of topics, these icons and accompanying marginal explanations placed at key points throughout the book are worded carefully to serve as both a preview and a review of key concepts, so that you may easily teach the topics in whatever order you wish. CONTENTS 1.

Introduction to Chemistry and Introduction to Active Learning.2 Matter and Energy3 Measurement and Chemical Calculations.4 Introduction to Gases5 Atomic Theory: The Nuclear Model of the Atom.6 Chemical Nomenclature.7 Chemical Formula and Relationships.8 Chemical Reactions9 Chemical Change.10 Quantity Relationships in Chemical Reactions.11 Atomic Theory: The Quantum Model of the Atom.12 Chemical Bonding13 Structure and Shape.14 The Ideal Gas Law and Its Applications15 Gases, Liquids, and Solids.16 Solutions17 AcidBase (Proton-Transfer) Reactions18 Chemical Equilibrium.19 Oxidation-Reduction (Electron Transfer) Reactions.20 Nuclear Chemistry21 Organic Chemistry.22 BiochemistryChapter SummariesAppendix I: Chemical Calculations. Appendix II: The SI System of Units.Glossary 2016, 720pp, Paperback, 9781305108981 INTRODUCTORY CHEMISTRY, 8E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Donald J. DeCoste, University of Illinois, Urbana-Champaign The Eighth Edition of Zumdahl

and DeCoste’s best-selling INTRODUCTORY CHEMISTRY that combines enhanced problem-solving structure with substantial pedagogy to enable students to become strong independent problem solvers in the introductory course and beyond. Capturing student interest through early coverage of chemical reactions, accessible explanations and visualizations, and an emphasis on everyday applications, the authors explain chemical concepts by starting with the basics, using symbols or diagrams, and conclude by encouraging students to test their own understanding of the solution. This step-by-step approach has already helped hundreds of thousands of students master chemical concepts and develop problem-solving skills. The book is known for its focus on conceptual learning and for the way it motivates students by connecting chemical principles to real-life experiences in chapter-opening discussions and “Chemistry in Focus” boxes. The Eighth Edition now adds a “questioning” pedagogy to in-text

examples to help students learn what questions they should be asking themselves while solving problems, offers a revamped art program to better serve visual learners, and includes a significant number of revised end-of-chapter questions. NEW TO THIS EDITION • The #1 online homework and learning system for chemistry, OWLv2, is available for this text-- www.cengageasiacom 89 Source: http://www.doksinet now with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader™, a new eBook with apps and embedded video, audio, annotations, and activities. OWLv2 courses for Gen Chem, GOB, and Liberal Arts now include Quick Prep essential skills assignments

that can be taken before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text and new iPad-compatible visualizations, tutorials, and simulations. FEATURES • The book’s full color art program has been modified and updated as needed to better serve visual learners. In addition, the art has been reconfigured for better clarity, glassware illustrations have been updated, and the orbital art has been redesigned all according to a new art and style program. Many new photos have been updated to give the textbook more relevance while also providing a contemporary look. • The text’s hallmark problem-solving pedagogy is enhanced by in-text examples that suggest what questions the students should be asking as they solve problems. • Almost all of the in-text examples are now “ Interactive Examples” and available online. These computer-based

examples throughout the text require students to think through the Example step-by-step rather than simply scan the written Example in the text as many students do. • New “Critical Thinking” boxes have been added at point-of-use throughout the text to emphasize the importance of conceptual learning. These are particularly useful for generating class discussion. • In Section 8.4 “Learning to Solve Problems” is written specifically to help students better understand how to think their way through a problem. 90 • In Chapter 9, the treatment of stoichiometry has been enhanced by the addition of a new section on limiting reactants, which emphasizes calculating the amounts of products that can be obtained from each reactant. Students are taught how to select a limiting reactant both by comparing the amounts of reactants present and by calculating the amounts of products that can be formed by complete consumption of each reactant. • The authors have revised a significant

number of the end-of-chapter questions (over 10%) while adding a new section for ChemWork problems, which are also available online. • The Eighth Edition is now supported by both OWL: Online Web Learning, the number one online learning system for chemistry, and Enhanced WebAssign. Both are available with e-books • Exercises and models such as worked-out examples, self-check exercises, and skill development boxes support the authors’ stepby-step problem-solving method. CONTENTS 1. Chemistry: An Introduction2 Measurements and Calculations.3 Matter4 Chemical Foundations: Elements, Atoms, and Ions.5 Nomenclature6 Chemical Reactions: An Introduction.7 Reactions in Aqueous Solutions.8 Chemical Composition9 Chemical Quantities.10 Energy11 Modern Atomic Theory.12 Chemical Bonding13 Gases14 Liquids and Solids.15 Solutions16 Acids and Bases17 Equilibrium.18 Oxidation–Reduction Reactions and Electrochemistry.19 Radioactivity and Nuclear Energy. 2015, 704pp, Paperback, 9781285453132

www.cengageasiacom Source: http://www.doksinet solution. This step-by-step approach has already helped numerous students master chemical concepts and develop problem-solving skills. The focus on conceptual learning and motivating students by connecting chemical principles to reallife experiences in chapter-opening discussions and “Chemistry in Focus” boxes require students to think through the Example step-by-step rather than simply scan the written Example in the text as many students do. NEW TO THIS EDITION INTRODUCTORY CHEMISTRY, 8E A Foundation, Hybrid Edition (with OWLv2 24-Months Printed Access Card) Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Donald J. DeCoste, University of Illinois, Urbana-Champaign Reflecting Cengage Learning’s commitment to offering flexible teaching solutions and value for students and instructors, this new hybrid version features the instructional presentation found in the printed text while delivering all the end-of chapter

exercises online in OWLv2, the leading online learning system for chemistry. The result-a briefer printed text that engages students online! Help your students improve their grades and understanding of concepts with this valuepacked Hybrid Edition. An access code to OWLv2 with MindTap Reader, is included with the text, providing students with powerful online resources that include tutorials, simulations, randomized homework questions, videos, a complete interactive electronic version of the textbook, and more! The Eighth Edition of Zumdahl and DeCoste’s best-selling INTRODUCTORY CHEMISTRY: A FOUNDATION combines enhanced problemsolving structure with substantial pedagogy to enable students to become strong independent problem solvers in the introductory course and beyond. Capturing student interest through early coverage of chemical reactions, accessible explanations and visualizations, and an emphasis on everyday applications, the authors explain chemical concepts by starting with

the basics, using symbols or diagrams, and conclude by encouraging students to test their own understanding of the • In Chapter 9, the treatment of stoichiometry has been enhanced by the addition of a new section on limiting reactants, which emphasizes calculating the amounts of products that can be obtained from each reactant. Students are taught how to select a limiting reactant both by comparing the amounts of reactants present and by calculating the amounts of products that can be formed by complete consumption of each reactant. • Interactive Examples, new for this edition, were added to engage students in the problem solving process as they are reading the text. These Interactive Examples require student input for each step in the example. The computer asks questions in the same way a teacher would when explaining a new concept. • Critical Thinking questions have been added throughout the text to emphasize the importance of conceptual learning. These are particularly useful

for generating class discussion. • New ChemWork end-of chapter problems have been added throughout the text. These problems test students’ understanding of core concepts from each chapter. Students who need help can get assistance through a series of online hints. The hints are usually in the form of interactive questions that guide students through the problem-solving process. Students cannot receive the correct answer from the computer; rather, it encourages students to continue working through the hints to arrive at the answer. ChemWork problems in the text can be worked using the online system or as pencil-and-paper problems. • Many of the Chemistry in Focus” boxes have been revised and new ones added with up-to-date topics such as Gorilla glass, nanocars, and using www.cengageasiacom 91 Source: http://www.doksinet breath analysis to diagnose disease. FEATURES • The book’s full color art program has been modified and updated as needed to better serve visual

learners. In addition, the art has been reconfigured for better clarity, glassware illustrations have been updated, and the orbital art has been redesigned all according to a new art and style program. Many new photos have been updated to give the textbook more relevance while also providing a contemporary look. • The text’s hallmark problem-solving pedagogy is enhanced by in-text examples that suggest what questions the students should be asking as they solve problems. • Almost all of the in-text examples are now “Interactive Examples” and available online. These computer-based examples throughout the text require students to think through the Example step-by-step rather than simply scan the written Example in the text as many students do. • New “Critical Thinking” boxes have been added at point-of-use throughout the text to emphasize the importance of conceptual learning. These are particularly useful for generating class discussion. • In Section 8.4 “Learning to

Solve Problems” is written specifically to help students better understand how to think their way through a problem. LAB MANUAL FOR ZUMDAHL/ DECOSTE’S INTRODUCTORY CHEMISTRY: A FOUNDATION, 8TH, 8E John G. Little Includes 35 experiments and eight appendices that serve as useful references. 2015, 368pp, Paperback, 9781285845166 CONTENTS 1. Chemistry: An Introduction2 Measurements and Calculations.3 Matter4 Chemical Foundations: Elements, Atoms, and Ions.5 Nomenclature6 Chemical Reactions: An Introduction.7 Reactions in Aqueous Solutions.8 Chemical Composition9 Chemical Quantities.10 Energy11 Modern Atomic Theory.12 Chemical Bonding13 Gases14 Liquids and Solids.15 Solutions16 Acids and Bases17 Equilibrium.18 Oxidation–Reduction Reactions and Electrochemistry.19 Radioactivity and Nuclear Energy.20 Organic Chemistry21 Biochemistry 2015, 592pp, Paperback, 9781285459707 92 www.cengageasiacom Source: http://www.doksinet INTRODUCTORY CHEMISTRY, 5E An Active Learning Approach,

International Edition Mark S. Cracolice, University of Montana; Edward I Peters Teach the course your way with INTRODUCTORY CHEMISTRY, 5E, International Edition. This text allows you to tailor the order of chapters to accommodate your particular needs, not only by presenting topics so they never assume prior knowledge but also by including any and all necessary preview or review information needed to learn that topic. The authors’ question-andanswer presentation allows students to actively learn chemistry while studying an assignment. This approach is reflected in three words of advice and encouragement that are repeated throughout the book: Learn It Now! This edition integrates new features such as outstanding technological resources, coached problems in a two-column format, and enhanced art and photography, all of which dovetail with the authors’ active learning approach. Even more flexibility is provided in the new edition by the Cengage YouBook, an electronic version of the

text that features interactivity, integrated media, and additional algebra coverage. NEW TO THIS EDITION • New Active Example Format: After observing students rush to apply an algorithm immediately after reading a problem statement, the authors redesigned the Active Example format. To encourage students to be less impulsive and slow down and analyze the problem statement before working on the solution, the first frame in every Active Example is labeled THINK BEFORE YOU WRITE. Subsequent steps are labeled as PLAN to help students consciously outline the solution to a problem. • New Two-Column Design for Active Examples: As students actively work through and complete the Active Example solution in the right column, they can reveal the solution to each step in the left column, thereby receiving immediate feedback about their understanding of the concept as it is being formed. Each example is also now titled so that students can better identify the concept or problem-solving skill

they are learning and can easily locate specific concepts to review when preparing for exams. • New Practice Exercises and Solutions: To solidify the potentially fragile new knowledge that the student just constructed during the process of completing the Active Example, each Active Example is now immediately followed by a parallel Practice Exercise that covers the same concept as the companion Active Examples, but is typically slightly more challenging. By pairing the Active Examples with Practice Exercises, the book leads students toward improved conceptual understanding and problem-solving skills. Solutions to this edition’s 241 Practice Exercises are provided in Appendix III. • New End-of-Chapter Illustrations: More than 100 new photographs and line drawings have been added to the end-of-chapter Questions, Exercises, and Problems to better illustrate the macroscopic aspect of chemistry and allow students to see physical and chemical changes and common forms of industrial

manufacturing processes, as well as better visualize the scenarios described in the questions. • Enhanced Features in OWL. OWL now includes Student Self-Assessments, as well as the interactive customizable Cengage YouBook, a multimedia electronic version of the text. FEATURES • Portable Chapter-in-Review Cards: Designed to make anywhere, anytime studying easier, these detachable cards at the back of the book include chapter summaries of goals and key concepts and a chapter self-test with answers. • Group Discussion Questions: These questions give students the opportunity to work together to develop their problem solving and conceptual www.cengageasiacom 93 Source: http://www.doksinet understanding. • Flexible Format: The book has been structured so that any common sequence of topics is supported, allowing professors to present topics in any order they prefer. • “Thinking About Your Thinking” Comments: Designed to encourage students to think the way chemists do and

focus on critical thinking, these features help students develop broad thinking skills they can apply to new contexts in future chemistry courses, other academic disciplines, and throughout their lives. • Section-Opening Learning Objectives: Identified as Goals, these objectives focus attention on what students are expected to learn or the skill they are expected to develop while studying the section. CONTENTS 1. Introduction to Chemistry; Introduction to Active Learning. 2 Matter and Energy 3 Measurement and Chemical Calculations. 4 Introduction to Gases 5. Atomic Theory: The Nuclear Model of the Atom 6. Chemical Nomenclature 7 Chemical Formula Relationships. 8 Chemical Reactions 9 Chemical Change. 10 Quantity Relationships in Chemical Reactions. 11 Atomic Theory: The Quantum Model of the Atom. 12 Chemical Bonding 13 Structure and Shape. 14 The Ideal Gas Law and Its Applications 15. Gases, Liquids, and Solids 16 Solutions 17. Acid-Base (Proton-Transfer) Reactions 18 Chemical

Equilibrium. 19 Oxidation-Reduction (Redox) Reactions. 20 Nuclear Chemistry 21 Organic Chemistry. 22 Biochemistry Appendix I: Chemical Calculations. Appendix II: The SI System of Units. Glossary Index 2013, 848pp, Paperback, 9781133108115 A BEGINNER’S GUIDE TO SCIENTIFIC METHOD, INTERNATIONAL EDITION, 4E Stephen S. Carey, Portland Community College This concise yet comprehensive guide provides an introduction to the scientific method of inquiry as well as detailed coverage of the many misapplications of scientific method that define pseudoscience. Compact enough to be used as a supplementary book in a science class, yet thorough enough in its coverage to be used as a core text in a class on scientific method, this text assists students in using the scientific method to design and assess experiments. NEW TO THIS EDITION • The explanations have been thoroughly to ensure clarity and readability for the student audience. • The discussion of causation in Chapter 3 has been greatly

expanded. • In Chapter 4, the basic framework for discussing experimental design has been revised to center on false confirmation and rejection. • In Chapter 5, the discussion of probability and statistical inference is greatly simplified. Each section now begins with and explains all points in terms of recent causal studies. • Two new pseudoscientific fallacies have been added and the text now contains many new and recent illustrations of all the fallacies. • Dozens of new exercises and examples have been added to every chapter. • End of chapter concept quizzes have been added. FEATURES • An introduction to the scientific method which 94 www.cengageasiacom Source: http://www.doksinet acknowledges that good science must remain utterly open to revision. • Over one hundred practical, relevant exercises and examples address common conceptual issues and pitfalls confronted in students’ own practices of scientific learning. • Real-life examples from scientific

literature provide immediate practical applications of the concepts encountered in the book. CONTENTS Preface.1 SCIENCE Just What is Science? Asking Why. Scientific Method The Consequences of Science. Scientific Method in Daily Life Things to Come. Exercises2 OBSERVATION Making Accurate Observations. Anomalous Phenomena Observing Anomalies. The Burden of Proof Concept Quiz. Exercises3 EXPLANATION Explanation, Theory and Hypothesis. Causation Correlation Causal Mechanisms. Underlying Processes Laws Function. The Interdependence of Explanatory Methods. Rival Explanations and Ockham’s Razor Explanation and Description. Ultimate Explanations Concept Quiz. Exercises4 EXPERIMENTATION The Basic Method. Confirmation and Rejection Designing a Good Test. Real World Experiments How Not to Design a Test. Conceptual Vagueness Testing Extraordinary Claims. Predictive Clarity Bias and Expectation. Concept Quiz Exercises5 ESTABLISHING CAUSAL LINKS. Causal Studies Ruling Out Chance. Multiple Causal

Factors Randomized, Prospective and Retrospective Studies. Reading Between the Lines Concept Quiz. Exercises6 FALLACIES IN THE NAME OF SCIENCE. What is a Fallacy? False Anomalies Questionable Arguments by Elimination. Illicit Causal Inferences. Unsupported Analogies and Similarities Untestable Explanations and Predictions. Empty Jargon. Ad Hoc Rescues Exploiting Uncertainty Science and Pseudoscience. Concept Quiz Exercises.FURTHER READINGINDEX 2012, 160pp, Paperback, 9781111726010 INTRODUCTION TO BASIC CHEMISTRY, INTERNATIONAL EDITION, 7E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Donald J. DeCoste, University of Illinois, Urbana-Champaign The Seventh Edition of INTRODUCTION TO BASIC CHEMISTRY, 7e, International Edition includes the first 16 chapters of INTRODUCTION TO CHEMISTRY: A FOUNDATION, 7e, International Edition. This new edition features a more explicit problem-solving pedagogy to help students develop critical thinking tools they can use in the

introductory course and beyond. Capturing student interest through early coverage of chemical reactions, accessible explanations and visualizations, and an emphasis on everyday applications, the authors explain chemical concepts by starting with the basics, using symbols or diagrams, and concluding by encouraging students to test their own understanding of the solution. This step-bystep approach has already helped hundreds of thousands of students master chemical concepts and develop problem-solving skills. The book is known for its focus on conceptual learning and for the way it motivates students by connecting chemical principles to real-life experiences in chapter-opening discussions and “Chemistry in Focus” boxes. The Seventh Edition now adds a “questioning” pedagogy to in-text examples to help students learn what questions they should be asking themselves while solving problems, offers a revamped art program to better serve visual learners, and includes a significant

number of revised end-of-chapter questions. The book’s unsurpassed teaching and learning resources www.cengageasiacom 95 Source: http://www.doksinet include a robust technology package that is now supported by OWL: Online Web Learning. NEW TO THIS EDITION • A significantly improved full color art program makes chemistry easier to understand for visual learners. • The text’s hallmark problem-solving pedagogy is enhanced by in-text examples that suggest what questions the students should be asking as they solve problems. • A new section in Chapter 8 explains why it is so important to become a good problem-solver. • The Seventh Edition is now supported by both OWL: Online Web Learning, the number one online learning system for chemistry. FEATURES • Exercises and models such as worked-out examples, self-check exercises, and skill development boxes support the authors’ stepby-step problem-solving method. • End-of-chapter material includes key terms, a summary of

important facts, questions and problems arranged in matched pairs and keyed to chapter sections, additional problems that incorporate material from multiple sections, inclass discussion questions, and “Cumulative Reviews” that test concepts from preceding chapters. • The text builds and refreshes fundamental math skills such as scientific notation, rounding, and rearranging equations. In addition, Math Tips, indicated by icons throughout, help students as they perform calculations. • The book is also available in alternative versions: INTRODUCTION TO CHEMISTRY; A FOUNDATION, International Edition, which includes five additional chapters that cover equilibrium, oxidation-reduction reactions and electrochemistry, radioactivity and nuclear energy, organic chemistry, and biochemistry.(Chapters 1-21) and INTRODUCTION TO CHEMISTRY, International Edition which include additional coverage of equilibrium, oxidation-reduction reactions, electrochemistry, radioactivity, and nuclear energy

(Chapters 1-19). 96 CONTENTS 1. CHEMISTRY: AN INTRODUCTIONChemistry: An Introduction. Chemistry in Focus: Dr Ruth Cotton Hero. What Is Chemistry? Solving Problems Using a Scientific Approach. Chemistry in Focus: A Mystifying Problem. The Scientific Method Learning Chemistry. Chemistry in Focus: Chemistry: An Important Component of Your Education.2 MEASUREMENTS AND CALCULATIONS.Scientific Notation. Units Chemistry in Focus: Critical Units! Measurements of Length, Volume, and Mass. Chemistry in Focus: Measurement: Past, Present, and Future. Uncertainty in Measurement Significant Figures. Problem Solving and Dimensional Analysis Temperature Conversions: An Approach to Problem Solving. Chemistry in Focus: Tiny Thermometers. Density3 MATTERMatter Physical and Chemical Properties and Changes. Elements and Compounds. Mixtures and Pure Substances. Chemistry in Focus: ConcreteAn Ancient Material Made New. Separation of Mixtures Cumulative Review for Chapters 1-3.4 CHEMICAL FOUNDATIONS:

ELEMENTS, ATOMS, AND IONS. The Elements. Chemistry in Focus: Trace Elements: Small but Crucial. Symbols for the Elements Dalton’s Atomic Theory. Chemistry in Focus: No Laughing Matter. Formulas of Compounds The Structure of the Atom. Chemistry in Focus: Glowing Tubes for Signs, Television Sets, and Computers. Introduction to the Modern Concept of Atomic Structure. Isotopes Chemistry in Focus: Isotope Tales. Introduction to the Periodic Table Chemistry in Focus: Putting the Brakes on Arsenic. Natural States of the Elements. Ions Compounds That Contain Ions.5 NOMENCLATURENaming Compounds. Chemistry in Focus: Sugar of Lead Naming Binary Compounds That Contain a Metal and a Nonmetal (Types I and II). Naming Binary Compounds That Contain Only Nonmetals (Type III). Naming Binary Compounds: A Review Naming Compounds That Contain Polyatomic Ions. Naming Acids Writing Formulas from Names Cumulative Review for Chapters 4-5.6 CHEMICAL REACTIONS: AN INTRODUCTION.Evidence for a Chemical Reaction.

Chemical Equations Balancing Chemical Equations. Chemistry in Focus: The Beetle That Shoots Straight.7 REACTIONS IN www.cengageasiacom Source: http://www.doksinet AQUEOUS SOLUTIONS.Predicting Whether a Reaction Will Occur. Reactions in Which a Solid Forms. Describing Reactions in Aqueous Solutions Reactions That Form Water: Acids and Bases. Reactions of Metals with Nonmetals (OxidationReduction). Ways to Classify Reactions Chemistry in Focus: Do We Age by Oxidation? Chemistry in Focus: Oxidation-Reduction Reactions Launch the Space Shuttle. Other Ways to Classify Reactions Cumulative Review for Chapters 6-7.8 CHEMICAL COMPOSITION.Counting by Weighing Chemistry in Focus: Plastic That Talks and Listens! Atomic Masses: Counting Atoms by Weighing. The Mole Molar Mass. Percent Composition of Compounds Formulas of Compounds. Calculation of Empirical Formulas. Calculation of Molecular Formulas9 CHEMICAL QUANTITIES.Information Given by Chemical Equations. MoleMole Relationships Mass

CalculationsChemistry in Focus: Methyl Alcohol: Fuel with a Future? Calculations Involving a Limiting Reactant. Percent Yield Cumulative Review for Chapters 8-9.10 ENERGYThe Nature of Energy. Temperature and Heat Exothermic and Endothermic Processes. Thermodynamics Measuring Energy Changes. Chemistry in Focus: Coffee: Hot and Quick(lime). Chemistry in Focus: Nature Has Hot Plants. Chemistry in Focus: Firewalking: Magic or Science? Thermochemistry (Enthalpy). Chemistry in Focus: Methane: An Important Energy Source. Hess’s Law Quality Versus Quantity of Energy. Energy and Our World Chemistry in Focus: Veggie Gasoline? Energy as a Driving Force.11 MODERN ATOMIC THEORY Rutherford’s Atom. Electromagnetic Radiation Chemistry in Focus: Light as a Sex Attractant. Chemistry in Focus: Atmospheric Effects 307. Emission of Energy by Atoms. The Energy Levels of Hydrogen. The Bohr Model of the Atom The Wave Mechanical Model of the Atom. The Hydrogen Orbitals. The Wave Mechanical Model: Further

Development. Electron Arrangements in the First Eighteen Atoms on the Periodic Table. Chemistry in Focus: A Magnetic Moment. Electron Configurations and the Periodic Table. Chemistry in Focus: The Chemistry of Bohrium. Atomic Properties and the Periodic Table. Chemistry in Focus: Fireworks12 CHEMICAL BONDING.Types of Chemical Bonds Electronegativity. Bond Polarity and Dipole Moments Stable Electron Configurations and Charges on Ions. Chemistry in Focus: Composite Cars Ionic Bonding and Structures of Ionic Compounds. Lewis Structures. Lewis Structures of Molecules with Multiple Bonds. Chemistry in Focus: Hiding Carbon Dioxide. Chemistry in Focus: BroccoliMiracle Food? Molecular Structure. Molecular Structure: The VSEPR Model. Chemistry in Focus: TasteIt’s the Structure That Counts. Molecular Structure: Molecules with Double Bonds. Chemistry in Focus: Minimotor Molecule. Cumulative Review for Chapters 10-12.13 GASESPressure Pressure and Volume: Boyle’s Law. Volume and Temperature:

Charles’s Law. Volume and Moles: Avogadro’s Law The Ideal Gas Law. Chemistry in Focus: Snacks Need Chemistry, Too! Dalton’s Law of Partial Pressures. Laws and Models: A Review The Kinetic Molecular Theory of Gases. The Implications of the Kinetic Molecular Theory. Gas Stoichiometry14 LIQUIDS AND SOLIDS.Water and Its Phase Changes. Energy Requirements for the Changes of State. Chemistry in Focus: Whales Need Changes of State. Intermolecular Forces Evaporation and Vapor Pressure. The Solid State: Types of Solids Bonding in Solids. Chemistry in Focus: Metal with a Memory.15 SOLUTIONSSolubility Chemistry in Focus: Green Chemistry. Solution Composition: An Introduction. Solution Composition: Mass Percent. Solution Composition: Molarity Dilution Stoichiometry of Solution Reactions. Neutralization Reactions. Solution Composition: Normality Cumulative Review for Chapters 13-15.16 ACIDS AND BASES.Acids and Bases Chemistry in Focus: Gum That Foams. Acid Strength Chemistry in Focus:

CarbonationA Cool Trick. Chemistry in Focus: Plants Fight Back. Water as an Acid and a Base. The pH Scale Chemistry in Focus: Airplane Rash. Chemistry in Focus: Garden-Variety AcidBase Indicators Calculating the pH of Strong Acid Solutions. Buffered SolutionsAPPENDIX Using Your Calculator. Basic Algebra Scientific (Exponential) Notation. Graphing Functions SI Units and Conversion Factors. Solutions to SelfCheck Exercises Answers to Even-Numbered End-of-Chapter Questions and Exercises. Answers to Even-Numbered Cumulative Review. Exercises www.cengageasiacom 97 Source: http://www.doksinet unsurpassed teaching and learning resources include a robust technology package that now offers OWL: Online Web Learning. Index/Glossary. Photo Credits 2011, 688pp, Paperback, 9780538736640 NEW TO THIS EDITION INTRODUCTION TO CHEMISTRY, 7E A Foundation, International Edition Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Donald J. DeCoste, University of Illinois, Urbana-Champaign

The Seventh Edition of Zumdahl and DeCoste’s best-selling INTRODUCTION TO CHEMISTRY: A FOUNDATION, International Edition that combines enhanced problem-solving structure with substantial pedagogy to enable students to become strong independent problem solvers in the introductory course and beyond. Capturing student interest through early coverage of chemical reactions, accessible explanations and visualizations, and an emphasis on everyday applications, the authors explain chemical concepts by starting with the basics, using symbols or diagrams, and conclude by encouraging students to test their own understanding of the solution. This step-bystep approach has already helped hundreds of thousands of students master chemical concepts and develop problem-solving skills. The book is known for its focus on conceptual learning and for the way it motivates students by connecting chemical principles to real-life experiences in chapter-opening discussions and “Chemistry in Focus”

boxes.The Seventh Edition now adds a “questioning” pedagogy to in-text examples to help students learn what questions they should be asking themselves while solving problems, offers a revamped art program to better serve visual learners, and includes a significant number of revised end-of-chapter questions. The book’s 98 • The book’s full color art program has been redrawn and reworked to make figures easier to follow and more aesthetically pleasing. In addition, labeling within the art has been reconfigured for better clarity, glassware illustrations have been updated, and the orbital art has been redesigned. • The text’s hallmark problem-solving pedagogy is enhanced by in-text examples that suggest what questions the students should be asking as they solve problems. • A new section in Chapter 8 explains why it is so important to become a good problem-solver. • The Seventh Edition is now supported by both OWL: Online Web Learning, the number one online learning

system for chemistry, and Enhanced WebAssign. Both are available with e-books. FEATURES • Exercises and models such as worked-out examples, self-check exercises, and skill development boxes support the authors’ stepby-step problem-solving method. • End-of-chapter material includes key terms, a summary of important facts, questions and problems arranged in matched pairs and keyed to chapter sections, additional problems that incorporate material from multiple sections, inclass discussion questions, and “Cumulative Reviews” that test concepts from preceding chapters. • The text builds and refreshes fundamental math skills such as scientific notation, rounding, and rearranging equations. In addition, Math Tips, indicated by icons throughout, help students as they perform calculations. • The book is also available in alternative versions: INTRODUCTION TO BASIC CHEMISTRY, International Edition, which covers chemical concepts and applications through acids and bases (Chapters

1-16) and INTRODUCTION TO CHEMISTRY, International Edition, which also covers equilibrium, oxidation-reduction reactions, www.cengageasiacom Source: http://www.doksinet electrochemistry, radioactivity, and nuclear energy (Chapters 1-19). CONTENTS 1. CHEMISTRY: AN INTRODUCTIONChemistry: An Introduction. Chemistry in Focus: Dr Ruth Cotton Hero. What Is Chemistry? Solving Problems Using a Scientific Approach. Chemistry in Focus: A Mystifying Problem. The Scientific Method Learning Chemistry. Chemistry in Focus: Chemistry: An Important Component of Your Education.2 MEASUREMENTS AND CALCULATIONS.Scientific Notation. Units Chemistry in Focus: Critical Units! Measurements of Length, Volume, and Mass. Chemistry in Focus: Measurement: Past, Present, and Future. Uncertainty in Measurement Significant Figures. Problem Solving and Dimensional Analysis Temperature Conversions: An Approach to Problem Solving. Chemistry in Focus: Tiny Thermometers Density.3 MATTERMatter Physical and Chemical

Properties and Changes. Elements and Compounds Mixtures and Pure Substances. Chemistry in Focus: ConcreteAn Ancient Material Made New. Separation of Mixtures. Cumulative Review for Chapters 1-3.4 CHEMICAL FOUNDATIONS: ELEMENTS, ATOMS, AND IONS.The Elements Chemistry in Focus: Trace Elements: Small but Crucial. Symbols for the Elements Dalton’s Atomic Theory. Chemistry in Focus: No Laughing Matter Formulas of Compounds. The Structure of the Atom Chemistry in Focus: Glowing Tubes for Signs, Television Sets, and Computers. Introduction to the Modern Concept of Atomic Structure. Isotopes Chemistry in Focus: Isotope Tales. Introduction to the Periodic Table. Chemistry in Focus: Putting the Brakes on Arsenic. Natural States of the Elements Ions Compounds That Contain Ions.5 NOMENCLATURE.Naming Compounds Chemistry in Focus: Sugar of Lead. Naming Binary Compounds That Contain a Metal and a Nonmetal (Types I and II). Naming Binary Compounds That Contain Only Nonmetals (Type III). Naming

Binary Compounds: A Review. Naming Compounds That Contain Polyatomic Ions. Naming Acids Writing Formulas from Names. Cumulative Review for Chapters 4-56 CHEMICAL REACTIONS: AN INTRODUCTION. Evidence for a Chemical Reaction. Chemical Equations. Balancing Chemical Equations Chemistry in Focus: The Beetle That Shoots Straight.7 REACTIONS IN AQUEOUS SOLUTIONS Predicting Whether a Reaction Will Occur. Reactions in Which a Solid Forms. Describing Reactions in Aqueous Solutions. Reactions That Form Water: Acids and Bases. Reactions of Metals with Nonmetals (Oxidation-Reduction). Ways to Classify Reactions. Chemistry in Focus: Do We Age by Oxidation? Chemistry in Focus: Oxidation-Reduction Reactions Launch the Space Shuttle. Other Ways to Classify Reactions. Cumulative Review for Chapters 6-7.8 CHEMICAL COMPOSITION Counting by Weighing. Chemistry in Focus: Plastic That Talks and Listens! Atomic Masses: Counting Atoms by Weighing. The Mole Molar Mass Percent Composition of Compounds. Formulas

of Compounds. Calculation of Empirical Formulas Calculation of Molecular Formulas.9 CHEMICAL QUANTITIES.Information Given by Chemical Equations. MoleMole Relationships Mass CalculationsChemistry in Focus: Methyl Alcohol: Fuel with a Future? Calculations Involving a Limiting Reactant. Percent Yield Cumulative Review for Chapters 8-9.10 ENERGYThe Nature of Energy Temperature and Heat. Exothermic and Endothermic Processes. Thermodynamics Measuring Energy Changes. Chemistry in Focus: Coffee: Hot and Quick(lime). Chemistry in Focus: Nature Has Hot Plants. Chemistry in Focus: Firewalking: Magic or Science? Thermochemistry (Enthalpy). Chemistry in Focus: Methane: An Important Energy Source. Hess’s Law. Quality Versus Quantity of Energy Energy and Our World. Chemistry in Focus: Veggie Gasoline? Energy as a Driving Force.11 MODERN ATOMIC THEORY.Rutherford’s Atom Electromagnetic Radiation. Chemistry in Focus: Light as a Sex Attractant. Chemistry in Focus: Atmospheric Effects 307. Emission of

Energy by Atoms. The Energy Levels of Hydrogen The Bohr Model of the Atom. The Wave Mechanical Model of the Atom. The Hydrogen Orbitals The Wave Mechanical Model: Further Development. Electron Arrangements in the First Eighteen Atoms on the Periodic Table. Chemistry in Focus: A Magnetic Moment. Electron Configurations and the Periodic Table. Chemistry in Focus: The Chemistry of Bohrium. Atomic Properties and the Periodic Table www.cengageasiacom 99 Source: http://www.doksinet Chemistry in Focus: Fireworks.12 CHEMICAL BONDING.Types of Chemical Bonds Electronegativity. Bond Polarity and Dipole Moments Stable Electron Configurations and Charges on Ions. Chemistry in Focus: Composite Cars. Ionic Bonding and Structures of Ionic Compounds. Lewis Structures. Lewis Structures of Molecules with Multiple Bonds. Chemistry in Focus: Hiding Carbon Dioxide. Chemistry in Focus: BroccoliMiracle Food? Molecular Structure. Molecular Structure: The VSEPR Model. Chemistry in Focus: TasteIt’s the

Structure That Counts. Molecular Structure: Molecules with Double Bonds. Chemistry in Focus: Minimotor Molecule. Cumulative Review for Chapters 10-12.13 GASESPressure Pressure and Volume: Boyle’s Law. Volume and Temperature: Charles’s Law. Volume and Moles: Avogadro’s Law The Ideal Gas Law. Chemistry in Focus: Snacks Need Chemistry, Too! Dalton’s Law of Partial Pressures. Laws and Models: A Review The Kinetic Molecular Theory of Gases. The Implications of the Kinetic Molecular Theory. Gas Stoichiometry14 LIQUIDS AND SOLIDS.Water and Its Phase Changes. Energy Requirements for the Changes of State. Chemistry in Focus: Whales Need Changes of State. Intermolecular Forces Evaporation and Vapor Pressure. The Solid State: Types of Solids Bonding in Solids. Chemistry in Focus: Metal with a Memory.15 SOLUTIONSSolubility Chemistry in Focus: Green Chemistry. Solution Composition: An Introduction. Solution Composition: Mass Percent Solution Composition: Molarity. Dilution Stoichiometry of

Solution Reactions. Neutralization Reactions. Solution Composition: Normality Cumulative Review for Chapters 13-15.16 ACIDS AND BASES.Acids and Bases Chemistry in Focus: Gum That Foams. Acid Strength Chemistry in Focus: CarbonationA Cool Trick. Chemistry in Focus: Plants Fight Back. Water as an Acid and a Base. The pH Scale Chemistry in Focus: Airplane Rash. Chemistry in Focus: Garden-Variety AcidBase Indicators Calculating the pH of Strong Acid Solutions. Buffered Solutions17 EQUILIBRIUM How Chemical Reactions Occur. Conditions That Affect Reaction Rates. Chemistry in Focus: Protecting the Ozone. The Equilibrium Condition Chemical Equilibrium: A Dynamic Condition. The 100 Equilibrium Constant: An Introduction. Heterogeneous Equilibria. Le Châtelier’s Principle Applications Involving the Equilibrium Constant. Solubility Equilibria. Cumulative Review for Chapters 16-17.18 OXIDATION-REDUCTION REACTIONS AND ELECTROCHEMISTRY.Oxidation-Reduction Reactions. Oxidation States

Oxidation-Reduction Reactions Between Nonmetals. Balancing OxidationReduction Reactions by the Half-Reaction Method Electrochemistry: An Introduction. Batteries Corrosion. Chemistry in Focus: Stainless Steel: It’s the Pits. Electrolysis Chemistry in Focus: WaterPowered Fireplace19 RADIOACTIVITY AND NUCLEAR ENERGY.Radioactive Decay Nuclear Transformations. Detection of Radioactivity and the Concept of Half-life. Dating by Radioactivity Chemistry in Focus: Dating Diamonds. Medical Applications of Radioactivity. Nuclear Energy Nuclear Fission. Nuclear Reactors Chemistry in Focus: Future Nuclear Power. Nuclear Fusion Effects of Radiation. Chemistry in Focus: Nuclear Waste Disposal.20 ORGANIC CHEMISTRY Carbon Bonding. Alkanes Structural Formulas and Isomerism. Naming Alkanes Petroleum Reactions of Alkanes. Alkenes and Alkynes Aromatic Hydrocarbons. Naming Aromatic Compounds Chemistry in Focus: Termite Mothballing. Functional Groups. Alcohols Properties and Uses of Alcohols Aldehydes and

Ketones. Naming Aldehydes and Ketones. Carboxylic Acids and Esters Polymers Chemistry in Focus: The Chemistry of Music. Chemistry in Focus: Polymers Are Tacky. B21 BIOCHEMISTRY. Proteins Primary Structure of Proteins. Secondary Structure of Proteins Tertiary Structure of Proteins. Functions of Proteins Enzymes. Chemistry in Focus: Urine Farming Carbohydrates. Chemistry in Focus: Great Expectations? The Chemistry of Placebos. Nucleic Acids. LipidsAPPENDIXUsing Your Calculator Basic Algebra. Scientific (Exponential) Notation Graphing Functions. SI Units and Conversion Factors. Solutions to Self-Check Exercises Answers to Even-Numbered End-of-Chapter Questions and Exercises. Answers to Even-Numbered Cumulative Review. Exercises Index/Glossary Photo Credits 2011, 848pp, Paperback, 9780538735438 www.cengageasiacom Source: http://www.doksinet • Several experiments have also been revised to provide clearer direction and more detail in the Procedure section. FEATURES INTRODUCTION TO

CHEMICAL PRINCIPLES, 7E A Laboratory Approach, International Edition Susan A. Weiner, West Valley College ; Blaine Harrison The seventh edition of this superb lab manual offers 36 class-tested experiments, suitable for introductory, preparatory, and health science chemistry courses and texts, including INTRODUCTORY CHEMISTRY: AN ACTIVE LEARNING APPROACH, 4e, INTERNATIONAL EDITION by Cracolice and Peters. Experiments in this lab manual teach students to collect and analyze experimental data and provide them with a strong foundation for further course work in general chemistry. This edition offers instructors a wide variety of experiments to customize their laboratory program, including many microscale experiments. All experiments can be completed in a three-hour laboratory period. As in the Sixth Edition, there are Work Pages for each experiment as well as Report Sheets for students to take notes and record experimental data and results, which facilitate instructor grading of

experiments. NEW TO THIS EDITION • The new edition features 11 worksheets covering the major topics of introductory chemistry. The worksheets can be used to enhance the lab experience or as supplementary homework. Complete solutions are available in the Instructor’s Manual. • The Seventh Edition also features four new experiments: “Experiment 27: Organic Nomenclature,” “Experiment 30: Esters,” “Experiment 34: Lipids,” and “Experiment 36: Enzymes.” • Duplicate Work Pages and Report Sheets for each experiment offer a convenient and efficient way for students to record their data as they work and yield clean, easy-to-grade reports. • Advance Study Assignments, to be completed before performing the experiments, require students to read the experiment before executing the lab, thus enabling them to complete the experiment in a safe and timely fashion. • Sample Calculations are presented to acquaint the student with the type of calculations they will be required

to perform for the experiment. • The lab manual features a variety of experiments for inorganic and organic chemistry so that it may accompany many different chemistry textbooks from introductory inorganic chemistry to allied health chemistry. CONTENTS SAFETY IN THE LABORATORY.LABORATORY PROCEDURES.EXPERIMENTS:1 Properties and Changes of Matter (m).2 The Chemistry of Some Household Products.3 Separation of Cations by Paper Chromatography (m).4 Densities of Liquids and Solids.5 Simplest Formula of a Compound (m).6 Hydrates (m)7 Percentage of Oxygen in Potassium Chlorate.8 Calorimetry.9 Chemical Names and Formulas: A Study Assignment.10 Chemical Equations: A Study Assignment.11 Mole Ratio for a Chemical Reaction (m).12 Types of Chemical Reactions (m).13 Qualitative Analysis of Some Common Ions (m).14 Separation of Cations15 Molecular Models: A Study Assignment.16 Molar Volume of a Gas (m).17 Molar Mass Determination by Freezing-Point Depression.18 The Conductivity of Solutions: A

Demonstration.19 Net Ionic Equations: A Study Assignment.20 Titration of Acids and BasesI.21 Titration of Acids and BasesII22 Determination of a Chemical Equation.23 A Study of Reaction Rates.24 Chemical Equilibrium (m)25 Measurement of pH with Indicators.26 Introduction to Oxidation-Reduction Reactions (m).27 Organic www.cengageasiacom 101 Source: http://www.doksinet Nomenclature.28 Hydrocarbons and Alcohols29 Aldehydes, Ketones, and Carboxylic Acids.30 Esters.31 Preparation of Aspirin32 Preparation and Properties of a Soap.33 Carbohydrates34 Lipids.35 Amino Acids and Proteins36 Enzymes WORKSHEETS:1. Significant Figures2 Dimensional Analysis.3 Avogrado’s NumberMoles4 Formula Writing5 Equation BalancingTypes of Reactions6 Stoichiometry7 Atomic Structure.8 Gases9 Solutions10 OxidationReduction11 Acids and BasesAppendix • • 2010, 480pp, Paperback, 9781439046647 • • and Equations highlight and clarify introductory chemistry issues for students, helping them to focus

on essential information and to maximize their study time. Sample Exercises: Providing step-by-step instruction, Sample Exercises include detailed explanations that guide students in gaining a solid understanding of chemistry concepts and principles. Avoiding Pitfalls: Included throughout the text, Caution icons alert students to common mistakes and help them avoid such missteps, making chemistry more accessible and easier to understand. Tips and Tools: Problem Solving Tips give students additional insight for successfully working through exercises and strengthening their analytical skills. You can order the SURVIVAL GUIDE FOR INTRODUCTORY CHEMISTRY in a convenient, money-saving package with either of these newer texts: Zumdahl/Zumdahl, INTRODUCTORY CHEMISTRY, 6E or Craccolice/Peters, INTRODUCTORY CHEMISTRY: AN ACTIVE LEARNING APPROACH, 4E. CONTENTS SURVIVAL GUIDE FOR INTRODUCTORY CHEMISTRY Charles H. Atwood, University of Georgia Straightforward, thorough, packed with examples and

exercises, and modeled after Atwood’s widely popular CHEMISTRY SURVIVAL GUIDE, the new SURVIVAL GUIDE FOR INTRODUCTORY CHEMISTRY is everything your students need to survive and thrive in an introductory course. Designed as a reader’s guide to an introductory textbook, the SURVIVAL GUIDE offers detailed step-by-step problem-solving sequences, giving students the competencyand confidencethey need to master the material and achieve optimal exam results. Coupled with a complementary math review, this brief but powerful resource covers the most fundamental aspects of introductory chemistry in a succinct series of essential modules. Module 1. An Approach to Problem SolvingModule 2. Metric System, Significant Figures, Dimensional Analysis, and Density.Module 3 Matter and Energy Module 4. Elements, Atoms and the Periodic Table Module 5. Chemical NomenclatureModule 6 Understanding Chemical Formulas and Using the Mole Concept.Module 7 Understanding Chemical Reaction Equations.Module 8

Chemical Reactions in Aqueous Solutions.Module 9 Chemical Reaction Stoichiometry.Module 10 Electronic Structure of Atoms.Module 11 Periodic Trends in Chemistry Module 12. Chemical BondingModule 13 Molecular Shapes and Polarity.Module 14 GasesModule 15 Liquids and Solids.Module 16 SolutionsModule 17 Acids and Bases.Module 18 Chemical Equilibrium Module 19. Oxidation-Reduction Reactions and Electrochemistry.Module 20 Nuclear Chemistry Math Review. 2009, 192pp, Paperback, 9780495828266 FEATURES • Student-friendly content: Key Terms, Concepts, 102 www.cengageasiacom Source: http://www.doksinet LIBERAL ARTS CHEMISTRY SURVIVAL GUIDE FOR GENERAL CHEMISTRY WITH MATH REVIEW, 2E Charles H. Atwood, University of Georgia Available for packaging with any CENGAGE textbook, this survival guide focuses on helping students practice for exams by showing them how to solve difficult problems by dissecting them into manageable chunks. The guide includes three levels of proficiency questions –

A, B, and minimal – to quickly build student confidence as they master the knowledge needed to succeed in the course. This book is also available for students to purchase separately at www.CENGAGEbraincom CONTENTS Module 1: Metric System, Dimensional Analysis, Significant Figures, and Density.Module 2: Understanding Chemical Formulas.Module 3: Chemical Nomenclature.Module 4: The Mole Concept.Module 5: Chemical Reaction Stoichiometry Module 6: Types of Chemical Reactions.Module 7: Electronic Structure of Atoms.Module 8: Chemical Periodicity.Module 9: Chemical BondingModule 10: Molecular Shapes.Module 11: Hybridization and Polarity of Molecules.Module 12: Acids and Bases.Module 13: States of MatterModule 14: Solutions.Module 15: Heat Transfer, Calorimetry, and Thermodynamics.Module 16: Chemical Kinetics.Module 17: Gas Phase EquilibriaModule 18: Aqueous Equilibria.Module 19: Electrochemistry Module 20: Nuclear Chemistry.Math Review 2008, 216pp, Paperback, 9780495387510 CHEM 2, 2E

Chemistry in Your World (with OWLv2 24-Months Printed Access Card) John L. Hogg, Texas A&M University Created by the continuous feedback of a “studenttested, faculty-approved” process, CHEM2 delivers a visually appealing, succinct print component, tear-out review cards for students and instructors, and a consistent online offering with OWLv2 that includes an eBook in addition to a set of interactive digital tools -- all at a value-based price and proven to increase retention and outcomes. CHEM2 also offers Go Chemistry and Thinkwell mini-video lectures, as well as online homework available through the OWL learning system. NEW TO THIS EDITION • END-OF-CHAPTER QUESTIONS have been added to nearly every chapter. • POWERPOINT LECTURE SLIDES, completely customizable to your specific classroom needs, help you prep for class faster and more efficiently. • NEW DETACHABLE EQUATION-SPECIFIC CARDS show students how to properly set up conversion and stoichiometric equations while

they do their homework. Each card features a “skeleton version” of the equation as well as an example. • A MORE USER-FRIENDLY, CHEMISTRYSPECIFIC DESIGN reflects the needs of today’s liberal arts students. • The #1 online homework and learning system for chemistry, OWLv2, is available for this text-- www.cengageasiacom 103 Source: http://www.doksinet • • • • • now with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader™, a new eBook withh apps and embedded video, audio, annotations, and activities. OWLv2 courses for Gen Chem, GOB, and Liberal Arts now include Quick Prep essential skills assignments that can be taken

before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text, 45 new visual exercises, and new iPad-compatible visualizations, tutorials, and simulations. EXTENSIVELY REORGANIZED CHAPTERS 2 AND 16 provide a better flow of subjects to enhance student understanding. THE UPDATED ART PROGRAM offers new and more relevant instructive images. DETACHABLE “CHAPTER IN REVIEW” CARDS, revised to match the text’s narrative, give students a portable study tool packed with pertinent information they can use to prepare for class. DETACHABLE “INSTRUCTOR PREP” CARDS -now including a list of the major revisions in each chapter -- make class prep quick and easy and include a quick map of chapter content, a list of corresponding PowerPoint and video resources, additional examples, and suggested assignments and discussion questions. RELEVANT, REAL LIFE

APPLICATIONS have been updated to reflect up-to-date issues affecting the chemical world. CONTENTS 1. Living in a World of Chemistry2 The Chemical View of Matter.3 Atoms and the Periodic Table4 The Air We Breathe.5 Chemical Bonding and States of Matter.6 Carbon Dioxide and the Greenhouse Effect.7 Chlorofl uorocarbons and the Ozone Layer.8 Chemical Reactivity: Chemicals in Action9 Acid--Base Reactions.10 Oxidation--Reduction 104 Reactions.11 Water, Water Everywhere but Not a Drop to Drink?12. Energy and Hydrocarbons13 Nuclear Changes and Nuclear Power.14 Organic Chemicals and Polymers.15 The Chemistry of Life.16 Nutrition: The Basis of Healthy Living17 Chemistry and Medicine.18 The Chemistry of Useful Materials.19 Feeding the WorldAppendices (Answers to Try Its & Answers to Selected Problems).Index 2015, 496pp, Paperback, 9781133962984 CHEM Melvin Joesten, Vanderbilt University ; John L. Hogg, Texas A&M University; Donald R. Neu, Saint Cloud State University CHEM delivers

exactly what today’s students need --and want. Based on student and faculty feedback from nationwide interviews and focus groups, CHEM was developed through a “student-tested, faculty-approved” process. The result is a concise, engaging, and accessible textbook that presents the basic chemical principles faculty require within a framework of relevant, real world applications that liberal arts students can relate to. Delivered at a value price, CHEM accommodates the diverse lifestyles of today’s learners, features a modern, open page design, and includes a wide array of print and online learning aids, including chapterby-chapter study cards, self-quizzes, interactive flash cards, Go Chemistry and Thinkwell mini-video lectures, and online homework available through the OWL learning system. FEATURES • Shorter, comprehensive chapters in a modern design, along with a wealth of print and online www.cengageasiacom Source: http://www.doksinet • • • • teaching and

learning aids, make this book ideal for today’s students. Detachable “Chapter in Review” cards give students a portable study tool packed with pertinent information they can use to prepare for class. Detachable “Instructor Prep” cards make class prep quick and easy and include a quick map of chapter content, a list of corresponding PowerPoint and video resources, additional examples, and suggested assignments and discussion questions. Learning tools designed to meet a wide range of learning styles include interactive quizzes, animations, videos, interactive and printable flashcards, and additional essays. Relevant, real- life applications feature such topics as the nutritional basis of healthy living, medicines and drugs, pollution & the conservation of natural resources, and the agricultural production of food for an ever-expanding world population. CONTENTS 1. Living in a World of Chemistry 2 The Chemical View of Matter. 3 Atoms and the Periodic Table 4 The Air We

Breathe and Some Major Atmospheric Pollutants. 5 Chemical Bonding and States of Matter. 6 Carbon Dioxide and the Greenhouse Effect. 7 Chlorofluorocarbons and the Ozone Layer. 8 Chemical Reactivity: Chemicals in Action 9. Acid-Base Reactions 10 Oxidation-Reduction Reactions. 11 Water, Water Everywhere, but Not a Drop to Drink? 12. Energy and Hydrocarbons 13 Nuclear Changes and Nuclear Power. 14 Organic Chemicals and Polymers. 15 The Chemistry of Life. 16 Nutrition: The Basis of Healthy Living 17. Chemistry and Medicine 18 The Chemistry of Useful Materials. 19 Feeding the World 2011, 448pp, Paperback, 9780538738217 ORGANIC CHEMISTRY A SMALL SCALE APPROACH TO ORGANIC LABORATORY TECHNIQUES, 4E Donald L. Pavia, Western Washington University; George S. Kriz, Western Washington University; Gary M Lampman, Western Washington University; Randall G. Engel, North Seattle Community College Featuring new experiments, a new essay, and new coverage of nanotechnology, this organic chemistry

laboratory textbook offers a comprehensive treatment of laboratory techniques including small-scale and some microscale methods that use standard-scale (“macroscale”) glassware and equipment. The book is organized based on essays and topics of current interest and covers a large number of traditional organic reactions and syntheses, as well as experiments with a biological or health science focus. Seven introductory technique-based experiments, thirteen project-based experiments, and sections on green chemistry and biofuels spark students’ interest and engage them in the learning process. Instructors may choose to offer Cengage Learning’s optional Premium Website, which contains videos on basic organic laboratory techniques. NEW TO THIS EDITION • This edition includes a new OWLv2 LabSkills program that can be bundled with the textbook. LabSkills provides students the opportunity to practice skills and prepare for real laboratory classes in a safe environment. Students work

through the assignments in advance of the lab www.cengageasiacom 105 Source: http://www.doksinet so they can actively rehearse common practical techniques by engaging with simulations, videos and quizzes. Because LabSkills focuses on techniques, instructors can customize assignments to align with the experiments that students will perform in any given lab session. The online course will also offer assessment specific to this edition’s experiments, and include a MindTap Reader. • New experiments in this edition: Experiment 24 - Preparation of Soap; Experiment 31 - A new green oxidation reaction using Oxone ® in An Oxidation-Reduction Scheme: Borneol, Camphor, Isoborneol; Experiment 44 - Preparation of Methyl Orange; Experiment 45 - Preparation of Indigo; Experiment 46 - Formulation of a Paint and Art Project. • New essays in this edition: Soap; Dyes. FEATURES • OWLv2 is the most trusted online learning solution for chemistry. Featuring chemist-developed content, OWLv2 is

the only system designed to elevate thinking through Mastery Learning, allowing students to work at their own pace until they understand each concept and skill. Each time a student tries a problem, OWLv2 changes the chemistry, values, and sometimes even the wording of the question to ensure students are learning the concepts and not cheating the system. With detailed, instant feedback and interactive learning resources, students get the help they need when they need it. Now with improved student and instructor tools and greater functionality, OWLv2 is more robust than ever. Discover the power of OWLv2 and take learning to a higher level. • The textbook contains a variety of well-written, comprehensive, and pre-tested small-scale experiments using standard-scale (macroscale) glassware and equipment. • Essays and examples on contemporary topics, such as biofuels and nanotechnology are provided to spark student interest and engage them in the learning process. • Green chemistry is

now better integrated due to its importance as a topic for students. • Infrared, proton NMR, and 13C NMR spectroscopy 106 is incorporated into many experiments. Some experiments also have an option to use gas chromatography-mass spectrometry. • The authors include introductory, techniquesbased experiments first to meet the needs of instructors who do not want to jump immediately into advanced material. CONTENTS Introduction.WELCOME TO ORGANIC CHEMISTRY.Laboratory Safety Organization of the Textbook. Advance Preparation Budgeting Time Purpose.PART I: INTRODUCTION TO BASIC LABORATORY TECHNIQUES.Experiment 1 Solubility.Experiment 2 CrystallizationExperiment 3. ExtractionExperiment 4 A Separation and Purification Scheme.Experiment 4A Extractions with a Separatory Funnel.Experiment 4B Extractions with a Screw-Cap Centrifuge TubeExperiment 5. Chromatography.Experiment 5A Thin-Layer Chromatography.Experiment 5B Selecting the Correct Solvent for Thin-Layer Chromatography. Experiment 5C.

Monitoring a Reaction with Thin Layer Chromatography.Experiment 5D Column Chromatography.Experiment 6 Simple and Fractional DistillationExperiment 7. Infrared Spectroscopy and Boiling-Point DeterminationEssay. Aspirin.Experiment 8 Acetylsalicylic AcidEssay Analgesics.Experiment 9 AcetaminophenEssay Identification of Drugs.Experiment 10TLC Analysis of Analgesic Drugs.Essay CaffeineExperiment 11 Isolation of Caffeine.Experiment 11A Extraction of Caffeine from Tea.Experiment 11B Isolation of Caffeine from a Tea Bag.Essay Esters--Flavors and Fragrances.Experiment 12: Isopentyl Acetate (Banana Oil).Essay, Terpenes and Phenylpropanoids Experiment 13. Isolation of Eugenol from Cloves Essay. Stereochemical Theory of OdorExperiment 14. Spearmint and Caraway Oil: (+)- and (-)CarvonesEssayThe Chemistry of Vision Experiment 15. Isolation of Chlorophyll and Carotenoid Pigments from Spinach.Essay: Ethanol and Fermentation Chemistry.Experiment 16 Ethanol from Sucrose.PART II: INTRODUCTION TO

MOLECULAR MODELING.Essay: Molecular Modeling and Molecular Mechanics.Experiment 17 An Introduction to Molecular Modeling.Experiment 17A. The Conformations of n-Butane: Local Minima www.cengageasiacom Source: http://www.doksinet Experiment 17B. Cyclohexane Chair and Boat Conformations.Experiment 17C Substituted Cyclohexane Rings (Critical Thinking Exercise). Experiment 17D. cis- and trans-2-ButeneEssay: Computational Chemistry - Ab initio and Semiempirical Methods.Experiment 18 Computational Chemistry.Experiment 18A Heats of Formation: Isomerism, Tautomerism, and Regioselectivity.Experiment 18B Heats of Reactions: SN1 Reaction Rates.Experiment 18C Density-Electrostatic Potential. Maps: Acidities of Carboxylic Acids.Experiment 18D Density -Electrostatic Potential Maps: Carbocations. Experiment 18E. Density -LUMO Maps: Reactivities of Carbonyl Groups.PART III: PREPARATIONS AND REACTIONS OF ORGANIC COMPOUNDS. Experiment 19. Reactivities of Some Alkyl Halides Experiment 20. Nucleophilic

Substitution Reactions: Competing NucleophilesExperiment 20A. Competing Nucleophiles with 1-Butanol or 2-Butanol.Experiment 20B. Competing Nucleophiles with 2-Methyl-2PropanolExperiment 20C AnalysisExperiment 21 Synthesis of n-Butyl Bromide and t-Pentyl Chloride. Experiment 21A. n-Butyl BromideExperiment 21B t-Pentyl Chloride.Experiment 22 4-MethylcyclohexenEssay. Fats and OilsExperiment 23. Methyl Stearate from Methyl OleateEssay: SoapExperiment 24. Preparation of SoapEssay: Petroleum and Fossil Fuels.Experiment 25 Gas Chromatographic Analysis of Gasolines.Essay: Biofuels.Experiment 26 BiodieselExperiment 26A Biodiesel from Coconut Oil.Experiment 26B Biodiesel from Other Oils.Experiment 26C Analysis of Biodiesel.Essay: Green ChemistryExperiment 27. Chiral Reduction of Ethyl Acetoacetate; Optical Purity Determination.Experiment 27A Chiral Reduction of Ethyl Acetoacetate.Experiment 27B NMR Determination of the Optical Purity of Ethyl (S)-3-Hydroxybutanoate.Experiment 28 Nitration of

Aromatic Compounds Using a Recyclable Catalyst. Experiment 29. Reduction of Ketones Using Carrots as Biological Reducing AgentsExperiment 30. Resolution of (+/-)-alpha-Phenylethylamine and Determination of Optical Purity.Experiment 30A Resolution of (+/-)-alpha-Phenylethylamine. Experiment 30B. Determination of Optical Purity Using NMR and a Chiral Resolving Agent.Experiment 31. An Oxidation-Reduction Scheme: Borneol, Camphor, Isoborneol.Experiment 32 Multistep Reaction Sequences: The Conversion of Benzaldehyde to Benzilic Acid.Experiment 32A Preparation of Benzoin by Thiamine Catalysis. Experiment 32B. Preparation of BenzilExperiment 32C. Preparation of Benzilic AcidExperiment 33 Triphenylmethanol and Benzoic Acid.Experiment 33A. TriphenylmethanolExperiment 33B Benzoic Acid.Experiment 34 Aqueous-Based Organozinc Reactions.Experiment 35 Sonogashira Coupling of Iodosubstituted Aromatic Compounds with Alkynes Using a Palladium Catalyst.Experiment 36 Grubbs Catalyzed Metathesis of

Eugenol with 1,4-Butenediol to Prepare a Natural Product.Experiment 37 The Aldol Condensation Reaction: Preparation of Benzalacetophenones (Chalcones).Experiment 38 A Green Enantioselective Aldol Condensation Reaction.Experiment 39 Preparation of an ,Unsaturated Ketone via Michael and Aldol Condensation Reactions.Experiment 40 Preparation of Triphenylpyridine.Experiment 41 1,4-Diphenyl1,3-ButadieneExperiment 42 Relative Reactivities of Several Aromatic Compounds.Experiment 43 Nitration of Methyl Benzoate.Essay: Synthetic Dyes Experiment 44. Preparation of Methyl Orange Experiment 45. Preparation of IndigoExperiment 46. Formulation of a Paint and Art ProjectEssay Local Anesthetics.Experiment 47 Benzocaine Essay. Pheromones: Insect Attractants and Repellants.Experiment 48 N,N-Diethyl-mtoluamide: The Insect Repellent “OFF”Essay: Sulfa Drugs.Experiment 49 Sulfa Drugs: Preparation of Sulfanilamide.Essay: Polymers and Plastics Experiment 50. Preparation and Properties of Polymers:

Polyester, Nylon, and Polystyrene. Experiment 50A. PolyestersExperiment 50B Polyamide (Nylon).Experiment 50C Polystyrene Experiment 50D. Infrared Spectra of Polymer Samples.Experiment 51 Ring-Opening Metathesis Polymerization (ROMP) Using a Grubbs Catalyst: A Three Step Synthesis of a Polymer.Experiment 51A. Diels-Adler ReactionExperiment 51B Conversion of the Diels-Adler Adduct to the Diester. Experiment 51C. Synthesizing the Polymer by RingOpening Metathesis Polymerization ROMP)Essay Diels–Alder Reaction and Insecticides.Experiment www.cengageasiacom 107 Source: http://www.doksinet 52. The Diels–Alder Reaction of Cyclopentadiene with Maleic Anhydride.Experiment 53 Diels-Adler Reaction with Anthracine-9-Methanol.Experiment 54. Photoreduction of Benzophenone and Rearrangement of Benzpinacol to Benzopinacolone. Experiment 54A. Photoreduction of Benzophenone Experiment 54B. Synthesis of -Benzopinacolone: The Acid-Catalyzed Rearrangement of Benzpinacol. Essay. Fireflies and

PhotochemistryExperiment 55 Luminol.Essay The Chemistry of Sweeteners Experiment 56. CarbohydratesExperiment 57 Analysis of a Diet Soft Drink by HPLC.Part IV: IDENTIFICATION OF ORGANIC SUBSTANCES. Experiment 58. Identification of Unknowns Experiment 58A. Solubility TestsExperiment 58B Tests for the Elements (N, S, X).Experiment 58C Tests for Unsaturation.Experiment 58D Aldehydes and Ketones.Experiment 58E Carboxylic Acids Experiment 58F. PhenolsExperiment 58G Amines Experiment 58H. AlcoholsExperiment 58I Esters PART V: PROJECT-BASED EXPERIMENTS. Experiment 59. Preparation of a C-4 or C-5 Acetate Ester.Experiment 60 Competing Nucleophiles in SN1 and SN2 Reactions: Investigations Using 2-Pentanol and 3-Pentanol.Experiment 61 FriedelCrafts AcylationExperiment 62 The Analysis of Antihistamine Drugs by Gas Chromatography-Mass Spectrometry.Experiment 63 Carbonation of an Unknown Aromatic Halide.Experiment 64 The Aldehyde Enigma.Experiment 65 Synthesis of Substituted Chalcones: A

Guided-Inquiry Experience.Experiment 66 Green Epoxidation of Chalcones.Experiment 67 Cyclopropanation Reactions of Chalcones.Experiment 68 Michael and Aldol Condensation Reactions.Experiment 69 Esterification Reactions of Vanillin: The Use of NMR to Determine a Structure.PART VI: THE TECHNIQUES.Technique 1 Laboratory Safety Technique 2. The Laboratory Notebook, Calculations, and Laboratory Records.Technique 3 Laboratory Glassware: Care and Cleaning.Technique 4 How to Find Data for Compounds: Handbooks and Catalogues.Technique 5 Measurement of Volume and Weight.Technique 6 Heating and Cooling Methods.Technique 7 Reaction MethodsTechnique 8. FiltrationTechnique 9 Physical Constants of Solids: The Melting Point.Technique 10 Solubility 108 Technique 11. Crystallization: Purification of Solids Technique 12. Extractions, Separations, and Drying Agents.Technique 13 Physical Constants of Liquids: The Boiling Point and Density.Technique 14. Simple DistillationTechnique 15 Fractional

Distillation, Azeotropes.Technique 16 Vacuum Distillation, Manometers.Technique 17 Sublimation Technique 18. Steam DistillationTechnique 19 Column Chromatography.Technique 20 Thin-Layer Chromatography.Technique 21 High-Performance Liquid Chromatography (HPLC).Technique 22 Gas Chromatography.Technique 23 Polarimetry Technique 24. RefractometryTechnique 25 Infrared Spectroscopy.Technique 26 Nuclear Magnetic Resonance Spectroscopy (Proton NMR). Technique 27. Carbon-13 Nuclear Magnetic Resonance Spectroscopy.Technique 28 Mass Spectrometry.Technique 29 Guide to the Chemical LiteratureAppendix 1: Tables of Unknowns and Derivatives.Appendix 2: Procedure for Preparing Derivatives.Appendix 3: Index of Spectra 2016, 1024pp, Hardback, 9781305253926 www.cengageasiacom Source: http://www.doksinet EXPERIMENTAL ORGANIC CHEMISTRY, 6E A Miniscale & Microscale Approach John C. Gilbert, Santa Clara University, Santa Clara, CA; Stephen F. Martin, University of Texas at Austin Providing even

more emphasis on inquiry-based learning and student collaboration and featuring three new green experiments and more than a dozen newly developed experiments, this Sixth Edition of Gilbert and Martin’s proven EXPERIMENTAL ORGANIC CHEMISTRY contains procedures for both miniscale (also known as small scale) and microscale users. The book offers an early focus on equipment, record keeping, and safety in the laboratory, and then guides students step by step through the theoretical and mechanistic principles underlying the experiments and the laboratory techniques needed to perform them with confidence. Students learn how to use a range of experimental techniques to synthesize compounds and analyze their properties, complete multi-step syntheses of organic compounds, and solve structures of unknown compounds. New experiments in Chapter 17 and 18 demonstrate the potential of chiral agents in fostering enantioselectivity and of performing solvent-free reactions. The bioorganic experiment in

Chapter 24 reflects the increasing emphasis on bioorganic chemistry in the course and gives students an opportunity to accomplish a mechanistically interesting and synthetically important coupling of two -amino acids to produce a dipeptide. NEW TO THIS EDITION • With three new green experiments and over a dozen newly developed experiments (in chapters 3, 10, and 14-20) this edition is considerably enhanced to provide a comprehensive lab experience for students. • To make room for new experiments, Chapters 25 (Identifying Organic Compounds) and 26 (The Literature of Organic Chemistry) have been moved online. • All images have been checked, with many revised and updated as needed. • New spectra have been added and are available online. • OWLv2 with LabSkills and MindTap Reader: Featuring chemist-developed content, OWLv2 with LabSkills is the only system designed to elevate thinking through Mastery Learning. Developed to prepare students for their lab sessions through

pre-lab assignments, this new OWLv2 course includes LabSkills pre-lab techniques, a MindTap Reader of the lab manual, and pre and postlab content specific to the experiments. With detailed, instant feedback and interactive learning resources, students get the help they need when they need it. FEATURES • Safety is emphasized through “Safety Alerts” and “Wrapping It Up” sections that highlight possible hazards and proper disposal of spent chemicals. • Fascinating “Historical Highlights” familiarize students with the lives of chemical pioneers who have advanced the field of chemistry. • Accurately drawn art shows students how to set up an experiment with confidence. • Margin drawings of equipment remind students about the set up for such techniques as distillation and reflux. • Each experiment begins with a thorough discussion of the theory and procedures involved and lays out experimental procedures in a clear format to enhance student understanding. CONTENTS 1.

Introduction, Record Keeping, and Laboratory Safety.2 Techniques and Apparatus3 Solids: Recrystallization and Melting Points.4 Liquids: Distillation and Boiling Points.5 Extraction6 www.cengageasiacom 109 Source: http://www.doksinet Chromatography.7 Stereoisomers8 Spectral Methods.9 Alkanes10 Alkenes11 Alkynes12 Dienes: The Diels-Alder Reaction.13 Kinetic and Thermodynamic Control of a Reaction.14 Nucleophilic Aliphatic Substitution: Preparation of Alkyl Halides.15 Electrophilic Aromatic Substitution.16 Oxidation of Alcohols and Carbonyl Compounds.17 Reduction Reactions of Double Bonds: Alkenes, Carbonyl Compounds, and lmines.18 Reactions of Carbonyl Compounds19 Organometallic Chemistry.20 Carboxylic Acids and Their Derivatives.21 Multistep Organic Synthesis.22 Polymers23 Carbohydrates24 Amino Acids and Peptides.25 Identifying Organic Compounds (ONLINE ONLY).26 The Literature of Organic Chemistry (ONLINE ONLY). 2016, 960pp, Hardback, 9781305080461 ORGANIC CHEMISTRY, 9E John E.

McMurry, Cornell University The most trusted and best-selling text for organic chemistry just got better! Updated with more coverage of nuclear magnetic resonance spectroscopy, expanded with new end-of-chapter mechanism problems and Practice Your Scientific Reasoning and Analysis questions, and enhanced with OWLv2, the latest version of the leading online homework and learning system for chemistry, John McMurry’s ORGANIC CHEMISTRY continues to set the standard for the course. The Ninth Edition also retains McMurry’s hallmark qualities: comprehensive, authoritative, and clear. McMurry has developed a reputation for crafting precise 110 and accessible texts that speak to the needs of instructors and students. More than a million students worldwide from a full range of universities have mastered organic chemistry through his trademark style, while instructors at hundreds of colleges and universities have praised his approach time and time again. NEW TO THIS EDITION • Discussions

of NMR spectroscopy and opportunities to practice mechanism problems have been expanded substantially for this 9th edition. • Mechanism problems at the ends of chapters are now grouped together so that they are easily located and recognized. • More than 200 new end-of-chapter problems have been added, with a particular emphasis on mechanism-drawing practice. • Nomenclature in many figures has been updated for consistency, so that infix numerical bonding positions appear immediately before the suffix. • Seven new Practice Your Scientific Analysis and Reasoning essays and corresponding MCATstyle questions, with topics focused on the latest developments in the medical, pharmaceutical or biological application of organic chemistry. • The most powerful online learning solution for chemistry is better than ever. OWLv2 now has more flexible student and instructor functionality, new personalized study tools, enhanced integration with learning management systems, and improved

analytics. For this course, OWLv2 also includes Quick Prep (a short course to review key chemistry concepts and essential skills), hundreds of new interactive versions of the endof-chapter questions from the text with hints and directed feedback, and Mechanism Activities, Tutors, Visualizations and Simulations that have been converted from Flash to HTML, allowing for easier navigation and streamlined grading. FEATURES • OWLv2 is the most trusted online learning solution for chemistry. Featuring chemist-developed content, OWLv2 is the only system designed to elevate thinking through Mastery Learning, allowing students to work at their own pace until www.cengageasiacom Source: http://www.doksinet they understand each concept and skill. Each time a student tries a problem, OWLv2 changes the, chemistry, values, and sometimes even the wording of the question to ensure students are learning the concepts and not cheating the system. With detailed, instant feedback and interactive

learning resources, students get the help they need when they need it. Now with improved student and instructor tools and greater functionality, OWLv2 is more robust than ever. Discover the power of OWLv2 and take learning to a higher level. • IMPROVED CHAPTER-ENDING PROBLEM ORGANIZATION. End-of-chapter problems are now grouped by type to assist professors in assigning problems and students in solving them. Mechanism-type problems have now been given their own section in chapters containing mechanism problems. • UNIQUE “VISUALIZING CHEMISTRY” PROBLEMS. These problems challenge students to make the essential connection between typical line-bond drawings and computer-generated molecular models. “Visualizing Chemistry” problems enhance your students’ ability to bridge the gap between the microscopic level of molecules and the macroscopic level of daily life. • HOLISTIC OVERVIEWS. At two key points, McMurry provides an “Overview” to help students grasp the subject

matter more holistically. The first “Overview” offers a review of organic mechanisms, while the second discusses the cohesiveness of carbonyl group reactions. Mustard Gas to Alkylating Anticancer Drugs12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy.13 Structure Determination: Nuclear Magnetic Resonance Spectroscopy.14 Conjugated Compounds and Ultraviolet Spectroscopy.15 Benzene and Aromaticity Practice Your Scientific Analysis and Reasoning III: Photodynamic Therapy (PDT)16. Chemistry of Benzene: Electrophilic Aromatic Substitution.17 Alcohols and Phenols.18 Ethers and Epoxides; Thiols and Sulfides.Preview of Carbonyl Chemistry.19 Aldehydes and Ketones: Nucleophilic Addition Reactions.Practice Your Scientific Analysis and Reasoning IV: SSRIs 20. Carboxylic Acids and Nitriles.21 Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions.22 Carbonyl AlphaSubstitution Reactions23 Carbonyl Condensation Reactions.Practice Your Scientific Analysis and

Reasoning V: Thymine in DNA24. Amines and Heterocycles.25 Biomolecules: Carbohydrates26 Biomolecules: Amino Acids, Peptides, and Proteins. Practice Your Scientific Analysis and Reasoning VI: Melatonin and Serotonin27. Biomolecules: Lipids28 Biomolecules: Nucleic Acids.29 The Organic Chemistry of Metabolic Pathways.30 Orbitals and Organic Chemistry: Pericyclic Reactions.31 Synthetic Polymers.Practice Your Scientific Analysis and Reasoning VII: The Potent Antibiotic of Endiandric Acid C. 2016, 1416pp, Hardback, 9781305080485 CONTENTS 1. Structure and Bonding2 Polar Covalent Bonds; Acids and Bases.3 Organic Compounds: Alkanes and Their Stereochemistry.4 Organic Compounds: Cycloalkanes and Their Stereochemistry5. Stereochemistry at Tetrahedral Centers.6 An Overview of Organic Reactions.7 Alkenes: Structure and Reactivity.Practice Your Scientific Analysis and Reasoning I: The Chiral Drug Thalidomide8. Alkenes: Reactions and Synthesis9 Alkynes: An Introduction to Organic Synthesis.10

Organohalides.11 Reactions of Alkyl Halides: Nucleophilic Substitutions and Eliminations.Practice Your Scientific Analysis and Reasoning II: From www.cengageasiacom 111 Source: http://www.doksinet CHEMICAL PRINCIPLES FOR ORGANIC CHEMISTRY ORGANIC CHEMISTRY, 3E Robert Boikess, Rutgers, the State University of New Jersey To help students succeed in the much tougher and more rigorous Organic Chemistry class, CHEMICAL PRINCIPLES FOR ORGANIC CHEMISTRY presents all of the necessary topics from General Chemistry in the way that organic chemists use them. The book helps students “unlearn” some of the approaches they learned in General Chemistry, learn new or different ones, and successfully apply concepts from General Chemistry to Organic Chemistry. FEATURES • This relatively short ancillary text presents all of the necessary topics from General Chemistry in the way organic chemists use them. • This book greatly simplifies the task of getting students up to speed in the Organic

Chemistry course by teaching them how to apply concepts from General Chemistry to Organic Chemistry. CONTENTS 1. Valence Bond Theory2 Molecular Orbital Theory.3 Acids and Bases4 Thermochemistry and Thermodynamics.5 Chemical Kinetics 2015, 224pp, Paperback, 9781285457697 112 With Biological Applications, Hybrid Edition (with OWLv2 24-Months Printed Access Card) John E. McMurry, Cornell University Renowned for its student-friendly writing style and fresh perspective, this fully updated Third Edition of John McMurry’s ORGANIC CHEMISTRY WITH BIOLOGICAL APPLICATIONS provides full coverage of the foundations of organic chemistry--enhanced by biological examples throughout. In addition, McMurry discusses the organic chemistry behind biological pathways. New problems, illustrations, and essays have been added. Media integration with OWL for Organic Chemistry, a customizable online learning system, and assessment tool, reduces faculty workload, facilitates instruction, and helps students

master concepts through tutorials, simulations, and algorithmically-generated homework questions. NEW TO THIS EDITION • WHY THIS CHAPTER? now begins each chapter; it is a brief introduction about the material being covered, why it is important and how the organic chemistry in the chapter relates to biological chemistry. • Figure and table references in the text are now in color to help reference them. All figure legends now begin with a boldface title to help students easily identify their content. • SOMETHING EXTRA essays end each chapter and tie the chapter content to relevant real-world material. Some new essays include, “Organic Foods,” and “Dental Anesthetics.” www.cengageasiacom Source: http://www.doksinet • Many new problems have been included at the end of chapters. • Some new content includes: Mercury-catalyzed alkyne hydration (Chapter 8); Enols and tautomerization (Chapter 8); Conversion of alcohols to alkyl fluorides (Chapter 12); Organic coupling

reactions (Chapter 12); Base-induced epoxide cleavage (Chapter 13); Killiani-Fischer and Whol degradation (Chapter 21); Prostaglandins and other eicosanoids (Chapter 23). • An increase in the number of Organic OWL questions for the online homework system. • The #1 online homework and learning system for chemistry, OWLv2, is available for this text-now with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader™, a new eBook with apps and embedded video. OWLv2 courses for Gen Chem, GOB, Organic, and Liberal Arts now include Quick Prep essential skills assignments that can be taken before the semester begins or during the first few weeks, to help

students succeed in the course. For this course, OWLv2 also includes new interactive versions of the endof-chapter questions from the text and new iPadcompatible visualizations and tutorials. FEATURES step in a reaction without having to jump back and forth between the text and structures. CONTENTS 1. Structure and Bonding2 Polar Covalent Bonds; Acids and Bases.3 Organic Compounds: Alkanes and Their Stereochemistry.4 Organic Compounds: Cycloalkanes and Their Stereochemistry.5 Stereochemistry at Tetrahedral Centers.6 An Overview of Organic Reactions.7 Alkenes and Alkynes.8 Reactions of Alkenes and Alkynes9 Aromatic Compounds.10 Structure Determination: Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet Spectroscopy.11 Structure Determination: Nuclear Magnetic Resonance Spectroscopy.12 Organohalides: Nucleophilic Substitutions and Eliminations.13 Alcohols, Phenols, and Thiols; Ethers and Sulfides: A Preview of Carbonyl Chemistry 14. Aldehydes and Ketones: Nucleophilic Addition

Reactions.15 Carboxylic Acids and Nitriles.16 Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions.17 Carbonyl AlphaSubstitution and Condensation Reactions18 Amines and Heterocycles.19 Biomolecules: Amino Acids, Peptides, and Proteins.20 Amino Acid Metabolism.21 Biomolecules: Carbohydrates22 Carbohydrate Metabolism.23 Biomolecules: Lipids and Their Metabolism.24 Biomolecules: Nucleic Acids and Their Metabolism.e25 Secondary Metabolites: An Introduction to Natural Products Chemistry.e26 Orbitals and Organic Chemistry: Pericyclic Reactions.e27 Synthetic Polymers 2015, 992pp, Paperback, 9781285867847 • EARLIER COVERAGE OF STEREOCHEMISTRY AND SPECTROSCOPY. Chirality and stereochemistry at tetrahedral centers, a topic crucial to understanding biological chemistry, appears early in Chapter 5. • ENHANCED PROBLEMS. To enhance problemsolving and visualization skills, McMurry uses many multi-step problems and reduces the number of drill-type problems. • VERTICAL FORMAT

FOR CHEMICAL AND BIOCHEMICAL REACTION MECHANISMS. Mechanisms are printed with action steps vertically, alongside annotations for each step next, so students can see what is occurring at each www.cengageasiacom 113 Source: http://www.doksinet • • CTE ORGANIC CHEMISTRY WITH CB COURSESMART EBOOK, 7E William H. Brown, Beloit College; Brent L Iverson, University of Texas, Austin; Eric Anslyn, University of Texas at Austin; Christopher S. Foote, University of California, Los Angeles Please note that the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies.Succeed in the course with this student-friendly, proven text. Designed throughout to help you master key concepts and improve your problem-solving skills, CHEMISTRY, Seventh

Edition includes a running margin glossary, end-of-chapter in-text mini study guides, a focus on “how to” skills, and more in-chapter examples and problems than any text on the market. To help you understand reaction mechanisms, the authors offset them in a stepwise fashion and emphasize similarities between related mechanisms using just four different characteristics: breaking a bond, making a new bond, adding a proton, and taking a proton away. Thoroughly updated throughout, the book offers numerous biological examples for premed students, unique roadmap problems, a wide range of in-text learning tools, and integration with an online homework and tutorial system, which now includes an interactive multimedia eBook. NEW TO THIS EDITION • MCAT PROBLEMS: To better prepare students for the upcoming new MCAT exam, the new edition 114 • • includes MCAT PRACTICE: PASSAGE AND PROBLEMS throughout the text. First students read the organic chemistry-related essay and then answer a

series of multiple-choice questions. NEW PRIMERS: Two new primers (Developing a Reaction Mechanism before Chapter 6 and Carboxylic Acid Derivative Reaction Mechanisms before Chapter 18) set key and possibly difficult concepts apart for easy reference to enhance student understanding. NEWLY-DRAWN ORGANIC CHEMISTRY REACTION ROADMAPS: Creating a cumulative, graphical representation of the different reactions students encounter in the context of important functional groups, the organic chemistry roadmaps help students visualize how to interconvert different functional groups (which often require different reactions from different chapters) by simply identifying the most direct path on the roadmap. New pull‐out cards show the roadmaps in sequential order. REVISED REACTION ROADMAP PROBLEMS: These unique problems relate to the authors’ organic chemistry roadmap (see above), which compares organic chemistry to a roadmap, with functional groups analogous to cities and reactions analogous to

the roads between them. FIVE NEW “HOW TO” BOXES: Integrated throughout the text at strategic points, the new boxes show students: “How To: Quickly Figure Out Formal Charge,” “How To: Quickly Recognize the Hybridization and Geometry of Atoms,” “How To: Quickly Draw and Recognize Enantiomers and Diastereomers,” “How To: Retrosynthetically Dissect an Amine into the Proper Starting Materials for a Reductive Amination,” and “How To: Recognize Aromatic Compounds: Criteria and Caveats.” CONTENTS 1. Covalent Bonding and Shapes of Molecules2 Alkanes and Cycloalkanes.3 Stereochemistry and Chirality.4 Acids and Bases5 AlkenesPrimer I: Reaction Mechanisms6. Reactions of Alkenes7 Alkynes.8 Haloalkanes, Halogenation, and Radical Reactions.9 Nucleophilic Substitution and B-Elimination.10 Alcohols11 Ethers, Sulfides, and Epoxides.12 Infrared Spectroscopy13 Nuclear www.cengageasiacom Source: http://www.doksinet Magnetic Resonance Spectroscopy.14 Mass Spectrometry.15

Introduction to Organometallic Compounds.16 Aldehydes and Ketones17 Carboxylic Acids.Primer II: Carboxylic Acid Derivative Reaction Mechanisms.18 Functional Derivatives of Carboxylic Acids.19 Enolate Anions and Enamines.20 Dienes, Conjugated Systems, and Pericyclic Reactions.21 Benzene and the Concept of Aromaticity.22 Reactions of Benzene and Its Derivatives.23 Amines24 Catalytic Carbon– Carbon Bond Formation.25 Carbohydrates26: Lipids.27 Amino Acids and Proteins28 Nucleic Acids.29 Organic Polymer ChemistryAppendices:1 Thermodynamics and the Equilibrium Constant.2 Major Classes of Organic Acids.3 Bond Dissociation Enthalpies.4 Characteristic 1H-NMR Chemical Shifts.5 Characteristic 13C Chemical Shifts6 Characteristic IR Absorption Frequencies.7 Electrostatic Potential Maps.8 Summary of Stereochemical Terms.9 Summary of the Rules of Nomenclature.10 Common Mistakes in Arrow Pushing.11 Organic Chemistry Roadmaps GLOSSARY G-1.INDEX I-1 2014, 920pp, Paperback, 9789814617833 ORGANIC

CHEMISTRY, HYBRID EDITION (WITH OWLV2 24-MONTHS PRINTED ACCESS CARD), 7E William H. Brown, Beloit College; Brent L Iverson, University of Texas, Austin; Eric Anslyn, University of Texas at Austin; Christopher S. Foote, University of California, Los Angeles Providing a modern introduction to organic chemistry for students majoring in chemistry, health, and the biological sciences, this revised and updated edition of ORGANIC CHEMISTRY is both student-friendly and cutting-edge and incorporates the latest advances in the field. Professors Brown, Iverson, and Anslyn have all won teaching awards at their respective schools, and they use their skills to build upon the text’s hallmarks of unified mechanistic themes, focused problem-solving, use of applied problems from the pharmaceutical field, and unrivaled visuals. Thoroughly updated throughout, the book offers numerous biological examples for pre-med students, a wide range of in-text learning tools, and integration with both a homework

and tutorial system and an interactive multimedia eBook. To help students understand reaction mechanisms, the authors offset them in a stepwise fashion and emphasize similarities between related mechanisms using just four different characteristics: breaking a bond, making a new bond, adding a proton and taking a proton away. Organic chemistry reaction roadmaps take a center stage in this edition with new pull-out maps designed in a stepwise manner by chapter. These roadmaps will help students to devise their own reaction pathways.Numerous resources help ensure student success in the course, including a www.cengageasiacom 115 Source: http://www.doksinet running margin glossary, a mini end-of-chapter intext study guide, and more in-chapter examples than any other text on the market. Emphasizing “howto” skills, this edition is packed with challenging synthesis problems, medicinal chemistry problems, and unique roadmap problems. NEW TO THIS EDITION • MCAT PROBLEMS: To better

prepare students for the upcoming new MCAT exam, the new edition includes MCAT PRACTICE: PASSAGE AND PROBLEMS throughout the text. First students read the organic chemistry-related essay and then answer a series of multiple-choice questions. • NEW PRIMERS: Two new primers (Developing a Reaction Mechanism before Chapter 6 and Carboxylic Acid Derivative Reaction Mechanisms before Chapter 18) set key and possibly difficult concepts apart for easy reference to enhance student understanding. • NEWLY-DRAWN ORGANIC CHEMISTRY REACTION ROADMAPS: Creating a cumulative, graphical representation of the different reactions students encounter in the context of important functional groups, the organic chemistry roadmaps help students visualize how to interconvert different functional groups (which often require different reactions from different chapters) by simply identifying the most direct path on the roadmap. New pull‐out cards show the roadmaps in sequential order. • REVISED REACTION

ROADMAP PROBLEMS: These unique problems relate to the authors’ organic chemistry roadmap (see above), which compares organic chemistry to a roadmap, with functional groups analogous to cities and reactions analogous to the roads between them. • FIVE NEW “HOW TO” BOXES: Integrated throughout the text at strategic points, the new boxes show students: “How To: Quickly Figure Out Formal Charge,” “How To: Quickly Recognize the Hybridization and Geometry of Atoms,” “How To: Quickly Draw and Recognize Enantiomers and Diastereomers,” “How To: Retrosynthetically Dissect an Amine into the Proper Starting Materials for a Reductive Amination,” and “How To: Recognize Aromatic Compounds: Criteria and Caveats.” 116 FEATURES • PRESENTATION OF MECHANISMS: Mechanisms are presented in a clear, stepwise fashion with written commentary accompanying each mechanistic step so verbal learners can learn alongside more visually oriented learners. Many mechanisms have been broken

into more steps to increase student understanding. In addition, the authors emphasize similarities between related mechanisms using just four different characteristics: breaking a bond, making a new bond, adding a proton, and taking a proton away. A new primer (right before Chapter 6) on Developing a Reaction Mechanism sets this material apart for easy reference. • VISUAL IMPACT: This text is distinguished by its striking, full-color art program (250 pieces of numbered art and over 1,000 pieces of in-text art). The Seventh Edition paints a detailed picture of the orbital nature of electron density in Chapter 1 by focusing on the interplay between the two complementary approaches to orbital descriptions: valence bond theory and molecular orbital theory. High-quality photos show organic chemistry as it occurs in the laboratory and in everyday life; electrostatic potential maps illustrate structure and reactivity; the spectra in the book reflects the latest imagery; and the book

includes state-of-the-art, mathematically accurate molecular models. • “HOW-TO” BOXES: To facilitate student success in the course, insightful “How-To” boxes highlight the survival skills necessary to learn and master organic chemistry. Integrated throughout the text at key points, these essential skills include “How To: Draw Curved Arrows and Push Electrons,” “How To: Draw Chiral Molecules,” “How To: Solve NMR Spectral Problems,” and many more. Five new How To boxes to this edition are, “How To: Quickly Figure Out Formal Charge,” “How To: Quickly Recognize the Hybridization and Geometry of Atoms,” “How To: Quickly Draw and Recognize Enantiomers and Diastereomers,” “How To: Retrosynthetically Dissect an Amine into the Proper Starting Materials for a Reductive Amination,” and “How To: Recognize Aromatic Compounds: Criteria and Caveats.” • BIOLOGY CONNECTION: Although still a www.cengageasiacom Source: http://www.doksinet predominantly

synthetic organic chemistry text, the book explicitly links concepts to biological chemistry topics--drawing in biology majors, pre-med students, and others who will soon go on to biochemistry. “Connections to Biological Chemistry” boxes discuss the applications of organic chemistry to biology to a wide range of topics. • REACTIONS IN CONTEXT: These problems apply organic chemistry to medicinal chemistry and the pharmaceutical sciences. CONTENTS 1. Covalent Bonding and Shapes of Molecules2 Alkanes and Cycloalkanes.3 Stereochemistry and Chirality.4 Acids and Bases5 AlkenesPrimer I: Reaction Mechanisms6. Reactions of Alkenes7 Alkynes.8 Haloalkanes, Halogenation, and Radical Reactions.9 Nucleophilic Substitution and B-Elimination.10 Alcohols11 Ethers, Sulfides, and Epoxides.12 Infrared Spectroscopy13 Nuclear Magnetic Resonance Spectroscopy.14 Mass Spectrometry.15 Introduction to Organometallic Compounds.16 Aldehydes and Ketones17 Carboxylic Acids.Primer II: Carboxylic Acid

Derivative Reaction Mechanisms.18 Functional Derivatives of Carboxylic Acids.19 Enolate Anions and Enamines.20 Dienes, Conjugated Systems, and Pericyclic Reactions.21 Benzene and the Concept of Aromaticity.22 Reactions of Benzene and Its Derivatives.23 Amines24 Catalytic Carbon–Carbon Bond Formation.25 Carbohydrates.26: Lipids27 Amino Acids and Proteins.28 Nucleic Acids29 Organic Polymer Chemistry.Appendices:1 Thermodynamics and the Equilibrium Constant.2 Major Classes of Organic Acids. 3 Bond Dissociation Enthalpies4 Characteristic 1H-NMR Chemical Shifts. 5 Characteristic 13C Chemical Shifts.6 Characteristic IR Absorption Frequencies.7 Electrostatic Potential Maps. 8 Summary of Stereochemical Terms9 Summary of the Rules of Nomenclature.10 Common Mistakes in Arrow Pushing.11 Organic Chemistry Roadmaps. GLOSSARY G-1INDEX I-1 2014, 1072pp, Paperback, 9781285426501 PUSHING ELECTRONS, 4E Daniel P. Weeks, Northwestern University This brief supplemental guidebook assists students in

mastering the difficult concept of pushing electrons that is essential to success in Organic Chemistry. With an investment of only 12 to 16 hours of self-study your students will have a better understanding of how to write resonance structures and will become comfortable with bond-making and bond-breaking steps in organic mechanisms. The low-tech, paper-on-pencil approach uses active involvement and repetition to teach students to properly push electrons to generate resonance structures and write organic mechanisms with a minimum of memorization. Compatible with any organic chemistry textbook. NEW TO THIS EDITION • All structures redrawn with attention to correcting all bond lengths and angles. • Updated and enhanced figures throughout the book. • A new chapter added on the mechanisms for making synthetic polymers. • A new section added on constitutional isomers. • A new section added on correcting common mechanistic mistakes. • Textual revisions to clarify some sections.

FEATURES • The key to the success of this book is that it knows its place. It is a supplement that should be assigned alongside a textbook, not as a textbook replacement or a standalone product. www.cengageasiacom 117 Source: http://www.doksinet The best way to market this book would be to convince ochem instructors that this will be a terrific 8-10 hr supplement that will be a great investment for getting their students up to speed with mechanisms. This step-by-step mechanistic approach fills an important hole that textbooks don’t cover. • Helps students master to critical concept of pushing electrons. • Entire program requires only 12 to 16 hours of students time through self-study. • A paper-on-pencil approach uses active involvement and repetition to teach the student. CONTENTS 1. Lewis Structures2 Resonance Structures3 Mechanisms.4 On Solving Mechanism Problems5 Some Reactiosn from Biochemistry. 2014, 224pp, Paperback, 9781133951889 A MICROSCALE APPROACH TO

ORGANIC LABORATORY TECHNIQUES, INTERNATIONAL EDITION, 5E Donald L. Pavia, Western Washington University; George S. Kriz, Western Washington University; Gary M Lampman, Western Washington University; Randall G. Engel, North Seattle Community College From biofuels, green chemistry, and nanotechnology, this proven laboratory textbook provides the up-todate coverage students need in their coursework and future careers. The book’s experiments, all designed to utilize microscale glassware and equipment, cover traditional organic reactions and syntheses, the isolation of natural products, and 118 molecular modeling and include project-based experiments and experiments that have a biological or health science focus. Updated throughout with new and revised experiments, new and revised essays, and revised and expanded techniques, the Fifth Edition is organized based on essays and topics of current interest. NEW TO THIS EDITION • A new essay on Biofuels enhances this edition’s “in the

news” topics. • Two new Green Chemistry experiments involve techniques such as solid phase extraction and the use of a microwave reaction system. • In two experiments, chiral gas chromatography is now included in the analysis of the products obtained. • Eight new experiments have been added: Experiment 2, Solubility; Experiment 27, Biodiesel; Experiment 34, Sonogashira Coupling of Iodosubstituted Aromatic Compounds with Alkynes Using a Palladium Catalyst; Experiment 35, Grubbs-Catalyzed Metathesis of Eugenol with 1,4-Butanediol to Prepare a Natural Product; Experiment 48: Diels-Alder Reaction with Anthracene-9-methanol; Experiment 59, Synthesis of Naproxen (Aleve®) by Palladium Catalysis; Experiment 62, Green Epoxidation of Chalcones; and Experiment 63, Cyclopropanation of Chalcones. • Four experiments have been revised: Experiment 31, An Oxidation-Reduction Scheme: Borneol, Camphor, Isoborneol; Experiment 44, N,NDiethyl-m-toluamide: The Insect Repellant “OFF”;

Experiment 52, Identification of Unknowns; and Experiment 56, Friedel-Crafts Acylation. • Essays on Petroleum and Fossil Fuels and The Chemistry of Sweeteners have been revised. • Four Techniques have been revised and expanded: Technique 7, Reaction Methods, has been extensively revised to include information on working under an inert atmosphere; Technique 12, Extractions, Separations, and Drying Agents, now includes new material on instructions on drawing separation schemes; Technique 25, Infrared Spectroscopy, now includes the use of ATR for infrared analysis of solids; and Technique 26, Nuclear Magnetic Resonance Spectroscopy, www.cengageasiacom Source: http://www.doksinet includes new material on analysis of diastereotopic protons. • A new method of obtaining boiling points and monitoring distillations using a temperature probe with one of the Vernier devices or a digital thermometer has been introduced. • The Cengage YouBook, an interactive, electronic version of the

lab manual, allows students to print and bring to the lab bench only the parts of the book they need, as well as to watch videos showing how each technique is executed. Quizzes in the YouBook test whether students understand the technique, and results of the quiz can be submitted to the instructor prior to entering the lab. FEATURES • Open-ended experiments allow students to “write” their own experimental procedures and make their own discoveries. CONTENTS PART I: INTRODUCTION TO BASIC LABORATORY TECHNIQUES.Experiment 1: Introduction to Microscale Laboratory.Experiment 2: Solubility Experiment 3: Crystallization.Experiment 4: Extraction.Experiment 5: A Separation and Purification Scheme.Experiment 6: Chromatography Experiment 7: Simple and Fractional Distillation. Experiment 8: Infrared Spectroscopy and Boiling Point Determination.ESSAY: AspirinExperiment 9: Acetylsalicylic Acid.ESSAY: Analgesics Experiment 10: Isolation of the Active Ingredient in an Analgesic Drug.Experiment

11: Acetaminophen ESSAY: Identification of Drugs.Experiment 12: TLC Analysis of Analgesic Drugs.ESSAY: Caffeine Experiment 13: Isolation of Caffeine.ESSAY: Esters -- Flavors and Fragrances.Experiment 14: Isopentyl Acetate (Banana Oil).ESSAY: Terpenes and Phenylpropanoids.Experiment 15: Essential Oils: Extraction of Oil of Cloves by Steam Distillation.Essay: Stereochemical Theory of Odor Experiment 16: Spearmint and Caraway Oil: (+)The Chemistry and (-)- Carvones.Essay: of Vision.Experiment 17: Isolation of Chlorophyll and Carotenoid Pigments from Spinach.Essay: Ethanol and Fermentation Chemistry.Experiment 18 Ethanol from Sucrose.PART II: INTRODUCTION TO MOLECULAR MODELING.ESSAY: Molecular Modeling and Molecular Mechanics.Experiment 19: An Introduction to Molecular Modeling. ESSAY: Computational Chemistry -- Ab initio and Semiempirical Methods.Experiment 20: Computational Chemistry.PART III: PROPERTIES AND REACTIONS OF ORGANIC COMPOUNDS. Experiment 21: Reactivities of Some Alkyl

Halides. Experiment 22: Nucleophilic Substitution Reactions: Competing Nucleophiles.Experiment 23: Synthesis of n-Butyl Bromide and t-Pentyl Chloride.Experiment 24: 4-Methylcyclohexene.ESSAY: Fats and Oils Experiment 25: Methyl Stearate from Methyl Oleate.ESSAY: Petroleum and Fossil Fuels Experiment 26: Gas Chromatographic Analysis of Gasolines.ESSAY: BiofuelsExperiment 27: Biodiesel.ESSAY: Green ChemistryExperiment 28: Chiral Reduction of Ethyl Acetoacetate; Optical Purity Determination Using a Chiral Shift Reagent. Experiment 29: Nitration of Aromatic Compounds Using a Recyclable Catalyst.Experiment 30: Resolution of (Phenylethylamine and Determination of Optical Purity.Experiment 31: An Oxidation-Reduction Scheme: Borneol, Camphor, Isoborneol.Experiment 32: Multi-Step Reaction Sequences: The Conversion of Benzaldehyde to Benzilic Acid.Experiment 33: Triphenylmethanol and Benzoic Acid.Experiment 34: Sonogashira Coupling of Iodosubstituted Aromatic Compounds with

Alkynes Using a Palladium Catalyst.Experiment 35: Grubbs-Catalyzed Metathesis of Eugenol with 1,4-Butanediol to Prepare a Natural Product. Experiment 36: Aqueous-based Organozinc Reactions.Experiment 37: The Aldol Condensation Reaction: Preparation of Benzalacetophenones (Chalcones).Experiment 38: Preparation of an -Unsaturated Ketone via Michael and Aldol Condensation Reactions.Experiment 39: The Wittig Reaction: Preparation of 1,4-Diphenyl-1,3butadiene.Experiment 40: Relative Reactivities of Several Aromatic Compounds.Experiment 41: Nitration of Methyl Benzoate.ESSAY: Local Anesthetics.Experiment 42: BenzocaineExperiment 43: Methyl Salicylate (Oil of Wintergreen).ESSAY: Pheromones: Insect Attractants and Repellents. Experiment 44: N,N-Diethyl-m-toluamide: The Insect Sulfa Drugs. Repellent “OFF.”ESSAY: Experiment 45: Sulfa Drugs: Preparation of www.cengageasiacom 119 Source: http://www.doksinet Sulfanilamide.Essay: Polymers and Plastics Experiment 46: Preparation and

Properties of Polymers: Polyester, Nylon, and Polystyrene.Essay: Diels-Alder Reactions and Insecticides.Experiment 47: The Diels-Alder Reaction of Cyclopentadiene with Maleic Anhydride.Experiment 48: Diels-Alder Reaction with Anthracene-9-methanol.Experiment 49: Photoreduction of Benzophenone and Rearrangement of Benzpinacol to Benzopinacolone. ESSAY:Fireflies and Photochemistry.Experiment 50: Luminol.ESSAY: The Chemistry of Sweeteners Experiment 51: Analysis of a Diet Soft Drink by HPLC.PART IV: IDENTIFICATION OF ORGANIC SUBSTANCES.Experiment 52: Identification of Unknowns.PART V: PROJECT-BASED EXPERIMENTS.Experiment 53: Preparation of a C-4 or C-5 Acetate Ester.Experiment 54: Isolation of Essential Oils from Allspice, Cloves, Cumin, Caraway, Cinnamon, Fennel, or Star Anise. Experiment 55: Competing Nucleophiles in SN1 and SN2 Reactions: Investigations using 2-Pentanol and 3-Pentanol.Experiment 56: Friedel-Crafts Acylation Experiment 57: The Analysis of Antihistamine Drugs by Gas

Chromatography-Mass Spectrometry. Experiment 58: The Use of Organozinc Reagents in Synthesis: An Exercise in Synthesis and Structure Proof by Spectroscopy.Experiment 59: Synthesis of Naproxen by Palladium Catalysis.Experiment 60: The Aldehyde Enigma.Experiment 61: Synthesis of Substituted Chalcones: A Guided-Inquiry Experience.Experiment 62: Green Epoxidation of Chalcones.Experiment 63: Cyclopropanation of Chalcones.Experiment 64: Michael and Aldol Condensation Reactions.Experiment 65: Esterification Reactions of Vanillin: The Use of NMR to Solve a Structure Proof Problem.Experiment 66: An Oxidation Puzzle.PART VI: THE TECHNIQUES Technique 1: Laboratory Safety.Technique 2: The Laboratory Notebook, Calculations, and Laboratory Records.Technique 3: Laboratory Glassware: Care and Cleaning.Technique 4: How to Find Data for Compounds: Handbooks and Catalogues. Technique 5: Measurement of Volume and Weight. Technique 6: Heating and Cooling Methods. Technique 7: Reaction Methods.Technique 8:

Filtration.Technique 9: Physical Constants of Solids: The Melting Point.Technique 10: Solubility 120 Technique 11: Crystallization: Purification of Solids. Technique 12: Extractions, Separations, and Drying Agents.Technique 13: Physical Constants of Liquids: The Boiling Point and Density.Technique 14: Simple Distillation.Technique 15: Fractional Distillation, Azeotropes.Technique 16: Vacuum Distillation, Manometers.Technique 17: Sublimation Technique 18: Steam Distillation.Technique 19: Column Chromatography.Technique 20: Thin-Layer Chromatography.Technique 21: High-Performance Liquid Chromatography (HPLC).Technique 22: Gas Chromatography.Technique 23: Polarimetry Technique 24: Refractometry.Technique 25: Infrared Spectroscopy.Technique 26: Nuclear Magnetic Resonance Spectroscopy.Technique 27: Carbon-13 Nuclear Magnetic Resonance SpectroscopyTechnique 28: Mass Spectrometry. Technique 29: Guide to the Chemical Literature. APPENDICES:Appendix 1: Tables of Unknowns and

Derivatives.Appendix 2: Procedures for Preparing Derivatives.Appendix 3: Index of Spectra 2013, 1040pp, Paperback, 9781133107415 www.cengageasiacom Source: http://www.doksinet ORGANIC CHEMISTRY Guided Inquiry for Recitation, Volume 2, International Edition Andrei Straumanis, College of Charleston Add the power of guided inquiry to your course without giving up lecture with ORGANIC CHEMISTRY: A GUIDED INQUIRY FOR RECITATION, Volume II, International Edition. Slim and affordable, the book covers key Organic 2 topics using POGIL (Process Oriented Guided Inquiry Learning), a proven teaching method that increases learning in organic chemistry. Containing everything you need to energize your teaching assistants and students during supplemental sessions, the workbook builds critical thinking skills and includes once-a-week, student-friendly activities that are designed for supplemental sessions, but can also be used in lab, for homework, or as the basis for a hybrid POGILlecture

approach. you. Each activity contains “The Big Picture” and “Common Points of Confusion” sections that steer students away from common pitfalls and toward an expert understanding of organic chemistry. • PROVEN EFFECTIVE IN INCREASING STUDENT LEARNING. Students learn best when they are actively engaged and thinking in class and working to solve problems and understand concepts the way real scientists do, by analyzing data and asking questions. The workbook activities improve student understanding of lectures and textbook reading and help them do better on exams. Special “To the Student” sections cover the nuts and bolts of using the workbook effectively. CONTENTS 1. Aromaticity2 Introduction to EAS 3 EAS Resonance Effects.4 EAS Competing Effects5 EAS Synthesis Workshop.6 Grignard and Lithium Reagents.7 Nucleophilic Addition-Elimination 8 Carboxylic Acids and Derivatives.9 Acid Halides and Anhydrides.10 Enol and Enolate Nucleophiles11 Aldol Reactions.12 Aldol

Condensations13 Claisen & Michael Reactions.14 Amines15 Carbon (13C) NMR.16 Proton (1H) NMRAppendixNW3: Naming Aromatic Compounds.NW4: Naming Carbonyl Compounds. 2012, 224pp, Paperback, 9781111578305 FEATURES • EASILY ADAPTABLE TO ANY ORGANIC CHEMISTRY COURSE. This workbook makes it easy for you to take advantage of the benefits of Process Oriented Guided Inquiry Learning (POGIL) without giving up lecture. • PERFECT FOR TEACHING ASSISTANTS OR UNDERGRADUATE PEER LEADERS. Designed to help you get more out of your TA or peer-led supplemental sessions, this workbook includes special “To the TA” sections that cover the nuts and bolts of a successful implementation. • A WIDE RANGE OF FLEXIBLE ACTIVITIES. Choose from among the diverse set of C”hemActivities “that cover key Organic 2 topics and use them in whatever order works best for www.cengageasiacom 121 Source: http://www.doksinet ORGANIC CHEMISTRY A Guided Inquiry for Recitation, Volume 1, International Edition

Andrei Straumanis, College of Charleston Confusion” sections that steer students away from common pitfalls and toward an expert understanding of organic chemistry. • PROVEN EFFECTIVE IN INCREASING STUDENT LEARNING. Students learn best when they are actively engaged and thinking in class and working to solve problems and understand concepts the way real scientists do, by analyzing data and asking questions. The workbook activities improve student understanding of lectures and textbook reading and help them do better on exams. Special “To the Student” sections cover the nuts and bolts of using the workbook effectively. CONTENTS Add the power of guided inquiry to your course without giving up lecture with ORGANIC CHEMISTRY: A GUIDED INQUIRY FOR RECITATION, Volume I, International Edition. Slim and affordable, the book covers key Organic 1 topics using POGIL (Process Oriented Guided Inquiry Learning), a proven teaching method that increases learning in organic chemistry.

Containing everything you need to energize your teaching assistants and students during supplemental sessions, the workbook includes once-a-week, student-friendly activities that are designed for supplemental sessions, but can also be used in lab, for homework, or as the basis for a hybrid POGIL-lecture approach. 1. Lewis Structures2 Resonance3 Constitutional Isomers.4 Cycloalkane Stereoisomers5 Alkene Stereoisomers.6 Addition to Alkenes7 Radical Halogenation.8 Chiral Centers9 Absolute Configuration (R/S).10 One-Step Nucleophilic Substitution (SN2).11 Two-Step Nucleophilic Substitution (SN1).12 Two-Step Elimination (E1).13 One-Step Elimination (E2)14 Sorting out E1, E2, SN1, SN2.15 Retrosynthesis16 Carbon (13C) NMR.17 Proton (1H) NMRAppendixNW1Nomenclature of AlkanesNW2-Introduction to Naming Functional Groups. 2012, 224pp, Paperback, 9781111578299 FEATURES • EASILY ADAPTABLE TO ANY ORGANIC CHEMISTRY COURSE. This workbook makes it easy for you to take advantage of the benefits of

Process Oriented Guided Inquiry Learning (POGIL) without giving up lecture. • PERFECT FOR TEACHING ASSISTANTS OR UNDERGRADUATE PEER LEADERS. Designed to help you get more out of your TA or peer-led supplemental sessions, this workbook includes special “To the TA” sections that cover the nuts and bolts of a successful implementation. • A WIDE RANGE OF FLEXIBLE ACTIVITIES. Choose from among 18 “ChemActivities” covering key Organic 1 topics and use them in whatever order works best for you. Each activity contains “The Big Picture” and “Common Points of 122 www.cengageasiacom Source: http://www.doksinet ORGANIC CHEMISTRY, 13E A Brief Course, International Edition Harold Hart, Michigan State University; Christopher M. Hadad, Ohio State University; Leslie E. Craine, Central Connecticut State University; David J. Hart, The Ohio State University The only textbook designed specifically for the onesemester short course in organic chemistry, this market leader appeals to

a range of non-chemistry science majors through its emphasis on practical, real-life applications, coverage of basic concepts, and engaging visual style. In contrast to other texts for the course that are streamlined versions of fullyear texts, this text was created from the ground up to offer a writing style, approach, and selection of topics that uniquely meet the needs of the short course. The Thirteenth Edition builds on the strengths of previous editions through an updated, dynamic art programonline, on CD, and in the textnew content that keeps students current with developments in the organic chemistry field, and a revised lab manual. NEW TO THIS EDITION • OWL INTEGRATION. Improve student learning outcomes with OWL, the #1 online homework and learning system for chemistry. Developed by chemistry instructors for teaching chemistry, OWL includes course management tools that make homework management a breeze, as well as advanced reporting and grade book features that save time in

grading homework and tracking student progress. OWL enables you to address students’ different learning styles through tutorials, simulations, visualization exercises, and algorithmically-generated homework questions with answer-specific feedback. With OWL’s mastery learning approach, students work at their own pace until they understand each concept/ skill. OWL includes an eBook, enhanced with multimedia learning tools. • UPDATED ART PROGRAM. The text’s updated, visually dynamic art program is enhanced online, on CD, and in the text. • UPDATED “A WORD ABOUT” ESSAYS. These engaging essaysnow assignable and accompanied by pedagogy motivate students by demonstrating how chemistry relates to other branches of science and to their everyday lives. Many of these essays examine emerging issues in green chemistry while others cover interesting topics such as Quinones and the Bombadier Beetle, Alkaloids and the Dart Poison Frog, Prostaglandins, and Aspirin and Pain. • UPDATED

“A CLOSER LOOK AT” BOXES. These updated boxes encourage students to develop their Web research skills by exploring topics ranging from mass spectrometry and carbon dating to Nobel laureates and protein chemistry to the polymerase chain reaction. Instructors may assign these activities, using them as a basis for class discussion or as a springboard for projects. FEATURES • VISUALLY DYNAMIC ART PROGRAM. The art program offers beautifully designed electrostatic potential maps to aid discussions of acid-base chemistry, as well as ball-and-stick structures that help students visualize molecules in three dimensions. • USE OF ARROW PUSHING FORMALISM. This assists professors teaching reaction mechanisms. • WORKED OUT EXAMPLES AND PRACTICE PROBLEMS. These exercises and problems guide students through learning and mastering chapter concepts. End-of-chapter problems gradually increase in difficulty, reinforcing basic principles and problem-solving skills before moving on to more

challenging ones. • ACCOMPANYING LABORATORY MANUAL. Developed with the assistance of co-author T.K Vinod at Western Illinois University, the lab manual includes an experiment on green chemistry, prelaboratory exercises, and safety instructions to students. www.cengageasiacom 123 Source: http://www.doksinet CONTENTS 1. Bonding and Isomerism2 Alkanes and Cyclalkanes; Conformational and Geometric Isomerism.3 Alkenes and Alkynes4 Aromatic Compounds.5 Stereoisomerism6 Organic Halogen Compounds; Substitution and Elimination Reactions.7 Alcohols, Phenols, and Thiols8 Ethers and Epoxides.9 Aldehydes and Ketones10 Carboxylic Acids and Their Derivatives.11 Amines and Related Nitrogen Compounds.12 Spectroscopy and Structure Determination.13 Heterocyclic Compounds.14 Synthetic Polymers15 Lipids and Detergents.16 Carbohydrates17 Amino Acids, Peptides, and Proteins.18 Nucleotides and Nucleic Acids. 2012, 608pp, Paperback, 9781111426248 ORGANIC CHEMISTRY, INTERNATIONAL EDITION, 8E John E.

McMurry, Cornell University The most trusted and best-selling text for organic chemistry just got better! Updated with the latest developments, expanded with more end-of-chapter problems, reorganized to cover stereochemistry earlier, and enhanced with OWL, the leading online homework and learning system for chemistry, John McMurry’s ORGANIC CHEMISTRY, 8e, International Edition continues to set the standard for the course. The Eighth Edition also retains McMurry’s hallmark qualities: comprehensive, authoritative, and clear. McMurry has developed a reputation for crafting precise and accessible texts that speak to the needs of instructors and students. More than a million students worldwide 124 from a full range of universities have mastered organic chemistry through his trademark style, while instructors at hundreds of colleges and universities have praised his approach time and time again. NEW TO THIS EDITION • IMPROVED CHAPTER-ENDING PROBLEM ORGANIZATION. End-of-chapter

problems are now grouped by type to assist professors in assigning problems and students in solving them. • EARLIER COVERAGE OF STEREOCHEMISTRY. Stereochemistry now appears earlier in the book (Chapter 5) to get to this important topic sooner in the course. In addition, Cahn–Ingold–Prelog sequence rules are now introduced in Section 5.5 • REVISISED COVERAGE OF FUNDAMENTAL TOPICS. The revision of activation energies in multistep reactions and the update of all bond dissociation energies in Chapter 6 helps students to better understand this fundamental topic. • REVISED END-OF-CHAPTER QUESTIONS IN OWL. The integrated OWL online learning system now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes an interactive e-version of the textbook, enhanced with rich multimedia learning tools

and available 24/7 in OWL. • REVISED “FOCUS ON” BOXES. These end-ofchapter boxes now present interesting applications of organic chemistry relevant to the particular chapter. • UPDATED FIGURES. To better coordinate legends with art, step numbers have been added to the legends of all mechanism figures. In addition, all figure references have been more clearly keyed to illustrations via color. • NEW SUPPLEMENT. SPARTAN MODEL: AN ELECTRONIC MODEL KIT is now available to package with the Eighth Edition for those who want to use this advanced technology resource. FEATURES • VERTICAL FORMAT FOR REACTION MECHANISMS. McMurry’s hallmark vertical format is used to explain reaction mechanisms. www.cengageasiacom Source: http://www.doksinet The mechanisms are printed vertically while explanations of the changes taking place in each step are printed next to the reaction arrow. This allows students to easily see what is occurring at each step in a reaction without having to jump

back and forth between the text and structures. • UNIQUE COVERAGE. McMurry emphasizes organic synthesis as a teaching device to help students organize and work with the large body of factual information that makes up organic chemistry. He also offers an unusually complete treatment of the organic chemistry of nucleic acids and an integrated treatment of polymer chemistry. • PROBLEM-SOLVING FOCUS. Each chapter contains many worked out examples with “Strategy Statements” that illustrate how to solve problems. Each practice problem and solution is then followed by a similar problem for the student to solve. This provides immediate problem-solving reinforcement for the student. CONTENTS 1. Structure and Bonding2 Polar Covalent Bonds; Acids and Bases.3 Organic Compounds: Alkanes and Their Stereochemistry.4 Organic Compounds: Cycloalkanes and Their Stereochemistry.5 Stereochemistry at Tetrahedral Centers.6 An Overview of Organic Reactions.7 Alkenes: Structure and Reactivity.8

Alkenes: Reactions and Synthesis.9 Alkynes: An Introduction to Organic Synthesis.10 Organohalides11 Reactions of Alkyl Halides: Nucleophilic Substitutions and Eliminations. 12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy.13 Structure Determination: Nuclear Magnetic Resonance Spectroscopy.14 Conjugated Compounds and Ultraviolet Spectroscopy.15 Benzene and Aromaticity16 Chemistry of Benzene: Electrophilic Aromatic Substitution.17 Alcohols and Phenols18 Ethers and Epoxides; Thiols and Sulfides.Preview of Carbonyl Chemistry.19 Aldehydes and Ketones: Nucleophilic Addition Reactions.20 Carboxylic Acids and Nitriles.21 Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions.22 Carbonyl Alpha-Substitution Reactions.23 Carbonyl Condensation Reactions.24 Amines and Heterocycles.25 Biomolecules: Carbohydrates26 Biomolecules: Amino Acids, Peptides, and Proteins.27 Biomolecules: Lipids28 Biomolecules: Nucleic Acids.29 The Organic Chemistry of Metabolic

Pathways.30 Orbitals and Organic Chemistry: Pericyclic Reactions.31 Synthetic Polymers. 2012, 1376pp, Paperback, 9780840054531 TECHNIQUES LABS FOR MACROSCALE AND MICROSCALE ORGANIC EXPERIMENTS (WITH COURSEMATE 2-SEMESTER PRINTED ACCESS CARD), 6E Kenneth L. Williamson, Mount Holyoke College, Emeritus; Katherine M. Masters, Pennsylvania State University Succeed in your organic laboratory course with TECHNIQUES LABS FOR MACROSCALE AND MICROSCALE ORGANIC EXPERIMENTS, Sixth Edition. This proven, authoritative manual emphasizes safety and features new experiments that stress greener chemistry, as well as updated NMR spectra and a Premium Website that includes glassware-specific videos with pre-lab, gradable exercises. Using the manual’s mix of macroscale and microscale experiments, you’ll gain the knowledge and confidence you need to perform a wide variety of experiments, as well as experience working with conventionally-sized glassware. NEW TO THIS EDITION • UPDATED NMR SPECTRA.

The authors have fully updated NMR spectra throughout the manual. • NEW AND UPDATED LABS AND EXPERIMENTS. Many labs have been updated, and new lab experiments include “A Diels-Alder Reaction www.cengageasiacom 125 Source: http://www.doksinet Puzzle: The Reaction of 2,4-Hexadien-1-ol with Maleic Anhydride” and “Multicomponent Reactions: The Aqueous Passerini Reaction, and Virstatin, a Possible Treatment for Cholera.” • NEW FOCUS ON GREEN CHEMISTRY. In addition to providing 10 new experiments that stress green chemistry, the authors offer tips on how to “think green” when doing the labs. • PREMIUM WEBSITE. A new Premium Website includes glassware-specific videos with pre-lab, gradable exercises. • ADDITIONAL EXPERIMENTS ON THE COMPANION WEBSITE. Experiments from the author’s best-selling MACROSCALE AND MICROSCALE ORGANIC EXPERIMENTS not included in this print manual are all available for download on the companion website of Analgesics and Isolating Lycopene

from Tomato Paste.9 Column Chromatography: Fluorenone, Cholesteryl Acetate, Acetylferrocene, and Plant Pigments.10 Gas Chromatography: Analysis of Alkene Isomers.11 Infrared Spectroscopy12 Nuclear Magnetic Resonance Spectroscopy.13 Mass Spectroscopy.14 Ultraviolet Spectroscopy, Refractive Indices, and Qualitative Instrumental Organic Analysis.15 Computational Chemistry 2012, 336pp, Paperback, 9781111430412 FEATURES • GREENER CHEMISTRY. Experiments that stress greener chemistry appear throughout the manual and are identified with a green chemistry icon. For example, the use of household bleach is explored as an alternative to the toxic chromium ion as an oxidizing agent for cyclohexanol. • AN EMPHASIS ON LABORATORY SAFETY. The laboratory safety chapter includes material on working with closed systems and laboratory courtesy. • A STRONG MASS SPECTROMETRY CHAPTER. The chapter on mass spectrometry describes time-of-flight and mass quadrupole analyzers and includes sections on GC-MS

and computer-aided spectral identification, as well as ESI and MALDI ionization. • BIOASSAY EXPERIMENTS. The manual’s bioassay experiments include a bioassay of eugenol isolated from cloves. • COMPREHENSIVE COVERAGE. Material is offered on diffuse reflectance IR analysis, capillary GC, and temperature programming. CONTENTS 1. Introduction2 Laboratory Safety, Courtesy, and Waste Disposal.3 Melting Points and Boiling Points.4 Recrystallization5 Distillation6 Steam Distillation, Vacuum Distillation, and Sublimation.7 Extraction.8 Thin-Layer Chromatography: Analysis 126 EXPERIMENTAL ORGANIC CHEMISTRY, 5E A Miniscale and Microscale Approach, International Edition Stephen F. Martin, University of Texas at Austin; John C Gilbert, Santa Clara University, Santa Clara, CA Providing even more emphasis on inquiry-based learning, a new green experiment, and more than a dozen new discovery experiments, this Fifth Edition of Martin and Gilbert’s proven Organic Chemistry Lab Experiments:

Miniscale & Microscale, International Edition contains procedures for both miniscale (also known as small scale) and microscale users. The manual first covers equipment, record keeping, and safety in the laboratory, then walks students step by step through the laboratory techniques they need to perform the book’s experiments with confidence. Chapters show students how to use the book’s techniques to synthesize compounds and analyze their properties, complete multistep syntheses of organic compounds, and solve structures of unknown compounds. A bioorganic experiment in Chapter 24 reflects the increasing emphasis on bioorganic chemistry in the course www.cengageasiacom Source: http://www.doksinet and gives students an opportunity to accomplish a mechanistically interesting and synthetically important coupling of two a-amino acids to produce a dipeptide. NEW TO THIS EDITION • This edition places even more emphasis on inquiry-based learning, with more than a dozen new

discovery experiments. • The fifth edition includes new and updated Historical Highlights on Polymorphs, Performance Enhancing Drugs, Acetylene, and Chiral Drugs. • Offers a new green experiment on the Bromination of (E)-Stilbene. • Includes video demonstrations of key techniques in the book in an optional new Premium Companion Website. The website also contains pre-lab exercises, proton NMR spectra for analyzing chemical shifts, integration, and coupling constants, IR spectra for analyzing functional groups, MSDS (material safety data sheets) tables for checking the safe handling of the materials in each experiment, and derivative tables. Chromatography.7 Stereochemistry8 Spectral Methods.9 Alkanes10 Alkenes11 Alkynes12 Dienes and the Diels-Alder Reaction.13 Kinetic and Thermodynamic Control of a Reaction.14 Nucleophilic Substitution 451.15 Electrophilic Aromatic Substitution.16 Oxidation 52517 Reduction.18 Carbonyl Compounds 58519 Organometallic Chemistry.20 Carboxylic Acids

and Their Derivatives.21 Multistep Synthesis .22 Polymers23 Carbohydrates-Amino Acids and Peptides.24 25 Identifying Organic Compounds.26 The Literature of Organic Chemistry 2011, 960pp, Paperback, 9781439049167 FEATURES • Emphasizes safety through Safety Alerts and Wrapping It Up sections that alert students to possible hazards and proper disposal of spent chemicals. • Includes fascinating Historical Highlights, brief essays that familiarize students with the lives of chemical pioneers who have advanced the field of chemistry. • Includes accurately drawn art to show students how to set up an experiment with confidence. • Includes margin drawings of equipment to remind students about the set up for such techniques as distillation and reflux. • This book helps students understand laboratory techniques by beginning each experiment with a thorough discussion of the theory and procedures involved and laying out experimental procedures in a clear format. CONTENTS 1.

Laboratory Overview2 Techniques and Apparatus.3 Recrystallization and Melting Points4 Distillation and Boiling Points .5 Extraction6 FUNDAMENTALS OF ORGANIC CHEMISTRY, INTERNATIONAL EDITION, 7E John E. McMurry, Cornell University Retaining the concise, to-the-point presentation that has already helped thousands of students move beyond memorization to a true understanding of the beauty and logic of organic chemistry, this Seventh Edition of John McMurry’s FUNDAMENTALS OF ORGANIC CHEMISTRY brings in new, focused content that shows students how organic chemistry applies to their everyday lives. In addition, redrawn chemical structures and artwork help students visualize important chemical concepts, a greater emphasis on biologically-related chemistry (including new problems) helps them grasp the enormous importance of organic chemistry in understanding the reactions that occur in living organisms, and new EOC problems keyed to OWL allow them to work text-specific problems online.

www.cengageasiacom 127 Source: http://www.doksinet Finally, for this edition, John McMurry reevaluated and revised his writing at the sentence level to ensure that the book’s explanations, applications, and examples are more student-friendly, relevant, and motivating than ever before. NEW TO THIS EDITION • The problem sets now include additional biologically-oriented problems in most chapters, shortened and focused “In the Medicine Cabinet’ and “In the Field” end-of-chapter problems, and new End of Chapter problems keyed to OWL that match the text to online homework. • Redrawn art and chemical structures (as well as computer-generated Orbitals) help students visualize chemistry processes and structures. • Titles have been added to Worked Examples to provide students with a frame of reference. • New “Why This Chapter?” explanations in chapter introductions explain the relevance of chapter material to students. • The book’s writing has been revised at the

sentence level to make the presentation even more student-friendly, relevant, and motivating. FEATURES • Clear explanations, thought-provoking examples, and an innovative vertical format for explaining reaction mechanisms make the text relevant and student-friendly. • Applied chapter openers with associated photos and molecular models help students see the relevance of chapter content. • The text’s full color presentation highlights the reacting parts of molecules and uses computergenerated ball-and-stick molecular models to aid students’ three-dimensional perception. • Nearly 100 electrostatic potential maps display the polarity patterns in molecules and the importance of these patterns in determining chemical reactivity. CONTENTS 1. Structure and Bonding; Acids and Bases2 The Nature of Organic Compounds: Alkanes.3 The Nature of Organic Reactions: Alkenes.4 Reactions of Alkenes and Alkynes.5 Aromatic Compounds6 Stereochemistry.7 Alkyl Halides8 Alcohols, 128 Phenols, and

Ethers.9 Aldehydes and Ketones: Nucleophilic Addition Reactions.10 Carboxylic Acids and Derivatives.11 Carbonyl Alpha-Substitution Reactions and Condensation Reactions.12 Amines INTERLUDE: THE ROADMAP OF CHEMICAL REACTIONS.13 Structure Determination14 Biomolecules: Carbohydrates.15 Biomolecules: Amino Acids, Peptides, and Proteins.16 Biomolecules: Lipids and Nucleic Acids.17 The Organic Chemistry of Metabolic Pathways. 2011, 672pp, Paperback, 9781439049730 INTRODUCTION TO ORGANIC LABORATORY TECHNIQUES, 3E A Small-Scale Approach, International Edition Randall G. Engel, North Seattle Community College; George S. Kriz, Western Washington University; Gary M Lampman, Western Washington University; Donald L. Pavia, Western Washington University Featuring new experiments, a new essay, and new coverage of nanotechnology, this organic chemistry laboratory textbook offers a comprehensive treatment of laboratory techniques including small-scale and some microscale methods that use

standard-scale (“macroscale”) glassware and equipment. The book is organized based on essays and topics of current interest and covers a large number of traditional organic reactions and syntheses, as well as experiments with a biological or health science focus. Seven introductory technique-based experiments, thirteen project-based experiments, and sections on green chemistry and biofuels spark students’ interest and engage them in the learning process. Instructors may choose to offer Cengage Learning’s optional www.cengageasiacom Source: http://www.doksinet Premium Website, which contains videos on basic organic laboratory techniques. NEW TO THIS EDITION • The Third Edition features a new essay, “Biofuels,” and two new experiments: Experiment 25, “Biodiesel” and Experiment 26, “Ethanol from Corn.” • Nanotechnology is introduced with a new demonstration in Experiment 1 forming a selfassembled monolayer (SAM). • Coverage of green chemistry is expanded and

revised; and all new spectra are included in Technique 26 “Nuclear Magnetic Resonance Spectroscopy (Proton NMR).” • An expanded section of project-based experiments now includes a new Experiment 64, “Green Epoxidation of Chalcones” and a new Experiment 65, “Cyclopropanation Reactions on Chalcones.” In all of these experiments, students must either solve a significant problem or they must generate all or part of a procedure. Intended to promote critical thinking, these experiments not only challenge students, but also give them a feeling of what it is like to “do” research in chemistry. FEATURES • The textbook contains a variety of well-written, comprehensive, and pre-tested small-scale experiments using standard-scale (macroscale) glassware and equipment. • Essays and examples on contemporary topics, such as biofuels and nanotechnology are provided to spark student interest and engage them in the learning process. • Green chemistry is now better integrated due

to its importance as a topic for students. • Infrared, proton NMR, and 13C NMR spectroscopy is incorporated into many experiments. Some experiments also have an option to use gas chromatography-mass spectrometry. • The authors include introductory, techniquesbased experiments first to meet the needs of instructors who do not want to jump immediately into advanced material. CONTENTS Introduction.WELCOME TO ORGANIC CHEMISTRY.Laboratory Safety Organization of the Textbook. Advance Preparation Budgeting Time Purpose.Part One: The TechniquesTechnique 1: Laboratory Safety.Technique 2: The Laboratory Notebook, Calculations, and Laboratory Records. Technique 3: Laboratory Glassware: Care and Cleaning.Technique 4: How to Find Data for Compounds: Handbooks and Catalogs.Technique 5: Measurement of Volume and Weight.Technique 6: Heating and Cooling Methods.Technique 7: Reaction Methods.Technique 8: FiltrationTechnique 9: Physical Constants of Solids: The Melting Point. Technique 10:

Solubility.Technique 11: Crystallization: Purification of Solids.Technique 12: Extractions, Separations, and Drying Agents. Technique 13: Physical Constants of Liquids: The Boiling Point and Density.Technique 14: Simple Distillation.Technique 15: Fractional Distillation, Azeotropes.Technique 16: Vacuum Distillation, Manometers.Technique 17: SublimationTechnique 18: Steam Distillation.Technique 19: Column Chromatography.Technique 20: Thin-Layer Chromatography.Technique 21: High-Performance Liquid Chromatography (HPLC).Technique 22: Gas Chromatography.Technique 23: Polarimetry Technique 24: Refractometry.Technique 25: Infrared Spectroscopy.Technique 26: Nuclear Magnetic Resonance Spectroscopy (Proton NMR). Technique 27: Carbon-13 Nuclear Magnetic Resonance Spectroscopy.Technique 28: 6 Mass Spectrometry.Technique 29: Guide to the Chemical Literature.Part Two: Introduction to Basic Laboratory Techniques.Experiment 1: SolubilityExperiment 2: Crystallization.Experiment 3:

ExtractionExperiment 4: A Separation and Purification Scheme.Experiment 4A: Extractions with a Separatory Funnel.Experiment 5: Chromatography.Experiment 5A: Thin-Layer Chromatography.Experiment 5B: Selecting the Correct Solvent for Thin-Layer Chromatography. Experiment 5C: Monitoring a Reaction with Thin Layer Chromatography.Experiment 5D: Column Chromatography.Experiment 6: Simple and Fractional Distillation.Experiment 7: Infrared Spectroscopy and Boiling-Point Determination. Experiment 8: Acetylsalicylic Acid.Experiment 9: Acetaminophen.Experiment 10: TLC Analysis of Analgesic Drugs.Experiment 11: Isolation of www.cengageasiacom 129 Source: http://www.doksinet Caffeine.Experiment 11A: Extraction of Caffeine from Tea.Experiment 11B: Isolation of Caffeine from a Tea Bag.Experiment 12: Isopentyl Acetate (Banana Oil).Experiment 13: Isolation of Eugenol from Cloves.Experiment 14: Spearmint and Caraway Oil: (+)- and (-)-Carvones.Experiment 15: Isolation of Chlorophyll and Carotenoid

Pigments from Spinach.Experiment 16: Ethanol from Sucrose Part Three: Introduction to Molecular Modeling. Experiment 17: An Introduction to Molecular Modeling.Experiment 17A: The Conformations of n-Butane: Local Minima.Experiment 17B: Cyclohexane Chair and Boat Conformations. Experiment 17C: Substituted Cyclohexane Rings (Critical Thinking Exercise).Experiment 17D: cisand trans-2-ButeneExperiment 18: Computational Chemistry.Experiment 18A: Heats of Formation: Isomerism, Tautomerism, and Regioselectivity. Experiment 18B: Heats of Reaction: SN1 Reaction Rates.Experiment 18C: Density–Electrostatic Potential Maps: Acidities of Carboxylic Acids. Experiment 18D: Density–Electrostatic Potential Maps: Carbocations.Experiment 18E: Density– LUMO Maps: Reactivities of Carbonyl Groups.Part Four: Preparations and Reactions of Organic Compounds.Experiment 19: Reactivities of Some Alkyl Halides.Experiment 20: Nucleophilic Substitution Reactions: Competing Nucleophiles. Experiment 20A:

Competitive Nucleophiles with 1-Butanol or 2-Butanol.Experiment 20B: Competitive Nucleophiles with 2-Methyl-2-Propanol.Experiment 20C: Analysis.Experiment 21: Synthesis of n-Butyl Bromide and t-Pentyl Chloride.Experiment 21A: n-Butyl Bromide.Experiment 21B: t-Pentyl Chloride Experiment 22: 4-Methylcyclohexene.Experiment 23: Methyl Stearate from Methyl Oleate.Experiment 24: Gas-Chromatographic Analysis of Gasolines. Experiment 25: Biodiesel.Experiment 25A: Biodiesel from Coconut Oil.Experiment 25B: Biodiesel from Other Oils.Experiment 25C: Analysis of Biodiesel Experiment 26: Ethanol from Corn.Experiment 27: Chiral Reduction of Ethyl Acetoacetate; Optical Purity Determination.Experiment 27A: Chiral Reduction of Ethyl Acetoacetate.Experiment 27B: NMR Determination of the Optical Purity of Ethyl (S)-3-Hydroxybutanoate.Experiment 28: Nitration of Aromatic Compounds Using a Recyclable Catalyst. 130 Experiment 29: Reduction of Ketones Using Carrots as Biological Reducing Agents.Experiment

30: Resolution of (±)-a-Phenylethylamine and Determination of Optical Purity.Experiment 30A: Resolution of (±)-a-Phenylethylamine.Experiment 30B: Determination of Optical Purity Using NMR and a Chiral Resolving Agent.Experiment 31: An Oxidation-Reduction Scheme: Borneol, Camphor, Isoborneol.Experiment 32: Multistep Reaction Sequences: The Conversion of Benzaldehyde to Benzilic Acid.Experiment 32A: Preparation of Benzoin by Thiamine Catalysis.Experiment 32B: Preparation of Benzil.Experiment 32C: Preparation of Benzilic Acid.Experiment 33: Triphenylmethanol and Benzoic Acid.Experiment 33A: Triphenylmethanol.Experiment 33B: Benzoic Acid Experiment 34: Aqueous-Based Organozinc Reactions.Experiment 35: Sonogashira Coupling of Iodosubstituted Aromatic Compounds with Alkynes using a Palladium Catalyst.Experiment 36: Grubbs Catalyzed Metathesis of Eugenol with 1,4-Butenediol to Prepare a Natural Product.Experiment 37: The Aldol Condensation Reaction: Preparation of Benzalacetophenones

(Chalcones).Experiment 38: A Green Enantioselective Aldol Condensation Reaction.Experiment 39: Preparation of an a,bUnsaturated Ketone via Michael and Aldol Condensation Reactions.Experiment 40: Preparation of Triphenylpyridine.Experiment 41: 1,4-Diphenyl1,3-ButadieneExperiment 42: Relative Reactivities of Several Aromatic Compounds.Experiment 43: Nitration of Methyl Benzoate.Experiment 44: Benzocaine.Experiment 45: N,N-Diethyl-mtoluamide: The Insect Repellent “OFF”Experiment 46: Sulfa Drugs: Preparation of Sulfanilamide. Experiment 47: Preparation and Properties of Polymers: Polyester, Nylon, and Polystyrene. Experiment 49A: Polyesters.Experiment 49B: Polyamide (Nylon).Experiment 49C: Polystyrene Experiment 49D: Infrared Spectra of Polymer Samples.Experiment 48: Ring-Opening Metathesis Polymerization (ROMP) Using a Grubbs Catalyst: A Three-Step Synthesis of a Polymer.Experiment 48A: Diels-Alder Reaction of Furan and Maleic Anhydride.Experiment 48B: Ring Opening of Anhydride in

Methanol.Experiment 48C: RingOpening Metathesis Polymerization (ROMP) www.cengageasiacom Source: http://www.doksinet Experiment 48A: Diels-Adler Reaction.Experiment 48B: Conversion of the Diels-Adler Adduct to the Diester.Experiment 48C: Synthesizing the Polymer by Ring-Opening Metathesis Polymerization (ROMP).Experiment 49: The Diels–Alder Reaction of Cyclopentadiene with Maleic Anhydride. Experiment 50: Diels-Alder Reaction with Anthracene-9-methanol.Experiment 51: Photoreduction of Benzophenone and Rearrangement of Benzpinacol to Benzopinacolone. Experiment 51A: Photoreduction of Benzophenone. Experiment 51B: Synthesis of b-Benzpinacolone: The Acid-Catalyzed Rearrangement of Benzpinacol. Experiment 52: Luminol.Experiment 53: Analysis of A Diet Soft Drink by HPLC.Experiment 54: Carbohydrates.Part Four: Identification of Organic Substances.Experiment 55: Identification of Unknowns.Experiment 55A: Solubility Tests Experiment 55B: Tests of the Elements (N, S, X).Experiment 55C:

Tests for Unsaturation Experiment 55D: Aldehydes and Ketones. Experiment 55E: Carboxylic Acids.Experiment 55F: Phenols.Experiment 55G: AminesExperiment 55H: Alcohols.Experiment 55I: EstersPart Six: ProjectBased ExperimentsExperiment 56: Preparation of a C-4 or C-5 Acetate Ester.Experiment 57: Isolation of Essential Oils from Allspice, Caraway, Cinnamon, Cloves, Cumin, Fennel, or Star Anise.Experiment 57A: Isolation of Essential Oils by Steam Distillation. Experiment 57B: Identification of the Constituents of Essential Oils by Gas Chromatography–Mass Spectrometry.Experiment 57C: Investigation of the Essential Oils of Herbs and SpicesA MiniResearch Project.Experiment 58: Competing Nucleophiles in SN1 and SN2 Reactions: Investigations Using 2-Pentanol and 3-Pentanol. Experiment 59: Friedel–Crafts Acylation.Experiment 60: The Analysis of Antihistamine Drugs by Gas Chromatography–Mass Spectrometry.Experiment 61: Carbonation of an Unknown Aromatic Halide. Experiment 62 The Aldehyde

Enigma.Experiment 63 Synthesis of Substituted Chalcones: A GuidedInquiry Experience.Experiment 64: Green Epoxidation of Chalcones.Experiment 65: Cyclopropanation Reactions on Chalcones. Experiment 66: Michael and Aldol Condensation Reactions.Experiment 67: Esterification Reactions of Vanillin: The Use of NMR to Determine at Structure.Experiment 68: An Oxidation PuzzlePart Seven: Essays.Essay 1: AspirinEssay 2: Analgesics Essay 3: Identification of Drugs.Essay 4: Caffeine Essay 5: EstersFlavors and Fragrances.Essay 6: Terpenes and Phenylpropanoids.Essay 7: Stereochemical Theory of Odor.Essay 8: The Chemistry of Vision.Essay 9: Ethanol and Fermentation Chemistry.Essay 10: Molecular Modeling and Molecular Mechanics.Essay 11: Computational Chemistryab Intio and Semiempirical Methods.Essay 12: Fats and Oils Essay 13: Petroleum and Fossil Fuels.Essay 14: Biofuels.Essay 15: Green ChemistryEssay 16: Local Anesthetics.Essay 17: Pheromones: Insect Attractants.Essay 18: Sulfa DrugsEssay 19:

Polymers and Plastics.Essay 20: Diels-Alder Reaction and Insecticides.Essay 21: Fireflies and Photochemistry.Essay 22: The Chemistry of Sweeteners.AppendicesAppendix 1: Tables of Unknowns and Derivatives.Appendix 2: Procedures for Preparing Derivatives.Appendix 3 Index of Spectra. 2011, 1024pp, Paperback, 9780538733281 www.cengageasiacom 131 Source: http://www.doksinet FEATURES ORGANIC EXPERIMENTS, 6E Macroscale and Microscale, International Edition Kenneth L. Williamson, Mount Holyoke College, Emeritus; Katherine M. Masters, Pennsylvania State University The market leader for the full-year organic laboratory, this manual derives many experiments and procedures from the classic Feiser lab text, giving it an unsurpassed reputation for solid, authoritative content. The Sixth Edition includes new experiments that stress greener chemistry, as well as updated NMR spectra and a Premium Website that includes glassware-specific videos with pre-lab, gradable exercises. Offering a

flexible mix of macroscale and microscale options for most experiments, this proven manual emphasizes safety and allows instructors to save on the purchase and disposal of expensive, sometimes hazardous, organic chemicals. Macroscale versions can be used for less costly experiments, allowing students to get experience working with conventionally-sized glassware. NEW TO THIS EDITION • UPDATED NMR SPECTRA. The authors have fully updated NMR spectra throughout the manual. • NEW AND UPDATED LABS AND EXPERIMENTS. Many labs have been updated, and new lab experiments include “A Diels-Alder Reaction Puzzle: The Reaction of 2,4-Hexadien-1-ol with Maleic Anhydride” and “Multicomponent Reactions: The Aqueous Passerini Reaction, and Virstatin, a Possible Treatment for Cholera.” • PREMIUM WEBSITE. A new Premium Website includes glassware-specific videos with pre-lab, gradable exercises. 132 • GREENER CHEMISTRY. Experiments that stress greener chemistry appear throughout the manual

and are identified with a green chemistry icon. For example, the use of household bleach is explored as an alternative to the toxic chromium ion as an oxidizing agent for cyclohexanol. • AN EMPHASIS ON LABORATORY SAFETY. The laboratory safety chapter includes material on working with closed systems and laboratory courtesy. • A STRONG MASS SPECTROMETRY CHAPTER. The chapter on mass spectrometry describes time-of-flight and mass quadrupole analyzers and includes sections on GC-MS and computer-aided spectral identification, as well as ESI and MALDI ionization. • BIOASSAY EXPERIMENTS. The manual’s bioassay experiments include a bioassay of eugenol isolated from cloves. • COMPREHENSIVE COVERAGE. Material is offered on diffuse reflectance IR analysis, capillary GC, and temperature programming. CONTENTS 1. Introduction2 Laboratory Safety, Courtesy, and Waste Disposal.3 Melting Points and Boiling Points.4 Recrystallization5 Distillation6 Steam Distillation, Vacuum Distillation, and

Sublimation.7 Extraction.8 Thin-Layer Chromatography: Analyzing Analgesics and Isolating Lycopene from Tomato Paste.9 Column Chromatography: Fluorenone, Cholesteryl Acetate, Acetylferrocene, and Plant Pigments.10 Gas Chromatography: Analyzing Alkene Isomers.11 Infrared Spectroscopy12 Nuclear Magnetic Resonance Spectroscopy.13 Mass Spectrometry.14 Ultraviolet Spectroscopy, Refractive Indices, and Qualitative Instrumental Organic Analysis.15 Computational Chemistry16 The SN2 Reaction: 1-Bromobutane.17 Nucleophilic Substitution Reactions of Alkyl Halides.18 Radical Initiated Chlorination of 1-Chlorobutane.19 Alkenes from Alcohols: Cyclohexene from Cyclohexanol.20 Bromination and Debromination: Purification of Cholesterol.21 Dichlorocarbene22 Oxidation: Cyclohexanol to Cyclohexanone; Cyclohexanone to Adipic Acid.23 The Cannizzaro Reaction: Simultaneous Synthesis of an Alcohol and an www.cengageasiacom Source: http://www.doksinet Acid in the Absence of Solvent.24 Oxidative Coupling of

Alkynes: 2,7-Dimethyl-3,5-octadiyn2,7-diol.25 Catalytic Hydrogenation26 Sodium Borohydride Reduction of 2-Methylcyclohexanone: A Problem in Conformational Analysis.27 Epoxidation of Cholesterol.28 Nitration of Methyl Benzoate.29 Friedel-Crafts Alkylation of Benzene and Dimethoxybenzene; HostGuest Chemistry.30 Alkylation of Mesitylene31 The Friedel-Crafts Reaction: Anthraquinone and Anthracene.32 Friedel-Crafts Acylation of Ferrocene: Acetylferrocene.33 Reactions of Triphenylmethyl Carbocation, Carbanion, and Radical.34 1,2,3,4-Tetraphenylnaphthalene via Benzyne.35 Triptycene via Benzyne36 Aldehydes and Ketones.37 Dibenzalacetone by the Aldol Condensation.38 Grignard Synthesis of Triphenylmethanol and Benzoic Acid.39 The Wittig and Wittig-Horner Reactions.40 Esterification and Hydrolysis.41 Acetylsalicylic Acid (Aspirin).42 Malonic Ester of a Barbiturate43 Amines.44 The Sandmeyer Reaction: 1-Bromo4-chlorobenzene, 2-Iodobenzoic Acid, and 4-Chlorotoluene.45 Synthesis and Bioassay of

Sulfanilamide and Derivatives.46 Dyes and Dyeing.47 Martius Yellow48 Diels-Alder Reaction.49 Ferrocene [Bis(cyclopentadienyl) iron].50 A Diels-Alder Reaction Puzzle: The Reaction of 2,4-Hexadien-1-ol with Maleic Anhydride.51 Tetraphenylcyclopentadienone52 Hexaphenylbenzene and Dimethyl Tetraphenylphthalate.53 The Benzoin Condensation: Catalysis by the Cyanide Ion and Thiamine.54 Nitric Acid Oxidation; Preparation of Benzil from Benzoin; and Synthesis of a .Heterocycle: Diphenylquinoxaline55 The Borohydride Reduction of a Ketone: Hydrobenzoin from Benzil.56 The Synthesis of 2,2-Dimethyl-1,5dioxolane; The Acetonide Derivative of a Vicinal Diol.57 1,4-Addition: Reductive Acetylation of Benzil.58 The Synthesis of an Alkyne from an Alkene; Bromination and Dehydrobromination: Stilbene and Diphenylacetylene.59 The Perkin Reaction: Synthesis of α-Phenylcinnamic Acid and Its Decarboxylation to cis-Stilbene.60 Multicomponent Reactions: The Aqueous Passerini Reaction.61 Chemiluminescence:

Syntheses of Cyalume and Luminol.62 Photochemistry: The Synthesis of Benzopinacol.63 Carbohydrates and Sweeteners.64 Virstatin, a Possible Treatment for Cholera.65 Biosynthesis of Ethanol and Enzymatic Reactions.66 The Synthesis of Natural Products: Pseudopellitierene and Camphor.67 Polymers: Synthesis and Recycling.68 Searching the Chemical Literature. 2011, 880pp, Paperback, 9780538733632 UNDERSTANDING THE PRINCIPLES OF ORGANIC CHEMISTRY A Laboratory Course, Reprint, International Edition Steven F. Pedersen, University of California - Berkeley; Arlyn M. Myers, University of California - Berkeley Class-tested by thousands of students and using simple equipment and green chemistry ideas, UNDERSTANDING THE PRINCIPLES OF ORGANIC CHEMISTRY: A LABORATORY COURSE, International Edition includes 37 experiments that introduce traditional, as well as recently developed synthetic methods. Offering upto-date and novel experiments not found in other lab manuals, this innovative book focuses

on safety, gives students practice in the basic techniques used in the organic lab, and includes microscale experiments, many drawn from the recent literature. An Online Instructor’s Manual available on the book’s instructor’s companion website includes helpful information, including instructors’ notes, prelab meeting notes, experiment completion times, answers to end-of-experiment questions, video clips of techniques, and more. FEATURES www.cengageasiacom 133 Source: http://www.doksinet • SAFETY NOTES in each experiment warn students about potential hazards, CHEMICAL SAFETY NOTES emphasize the proper handling of reagents, and TECHNIQUE TIPS give students guidelines for handling equipment and using proper procedures. • REFERENCES TO TOPICS IN UNDERGRADUATE TEXTBOOKS and/or the primary literature in the experiments reinforce the importance of what students are learning in the lecture course and demonstrate how text material relates to the laboratory. • INTRODUCTORY

ESSAYS in the experiments expose students to the history and practical applications of laboratory science. Within many experiments, “DID YOU KNOW?” boxes provide a brief, interesting fact about one of the chemicals used in the experiment. • A CONSISTENT FORMAT for each experiment includes Background Reading, Prelab Checklist, Experimental Procedure, and Cleanup. • Instructors may choose to offer the optional PREMIUM ORGANIC CHEMISTRY LABORATORY TECHNIQUES WEBSITE, which contains 33 videos on basic organic laboratory techniques. Each video has a series of questions with instant grading and feedback, so students can test their understanding of the concepts and email their assessment results to their instructors. CONTENTS PART I: THE THEORY AND TECHNIQUES.1 Safety in the Chemistry Lab.2 The Laboratory Notebook and the Laboratory Period.3 Where to Find It: Searching the Literature.4 Things You Need to Know Before You Begin.5 Properties of Organic Molecules.6 Characteristic Physical

Properties of Pure Compounds.7 Isolation and Purification of Compounds.8 Structure Determination9 Running a Synthetic Reaction. PART II: THE EXPERIMENTS Experiment 1. Calibrating a Pasteur Pipette Experiment 2. Investigating Solubility and Acid-Base Reactions.Experiment 3 Mixed Melting Points Experiment 4. Whittling Down the Possibilities: Identifying an Unknown Using Molecular Dipole Moment, Solubility, Density and Boiling Point Data.Experiment 5 Recrystallization and Melting Points: Recrystallization of Adipic and Salicylic 134 Acids. Experiment 6 Recrystallization and Melting Points: Recrystallization of an Unknown Solid and the Decolorization of Brown Sugar.Experiment 7 Thin Layer Chromatography (TLC).Experiment 8 Identification of an Adulterated Herb or Spice by Thin Layer Chromatography (TLC).Experiment 9 What Do You Take for Pain? Experiment 10. Nucleophilic Substitution Reactions of Alkyl Halides.Experiment 11. The Isolation of Trimyristin from Nutmeg Experiment 12. The

Magtrieve™ Oxidation of 4-Chlorobenzyl Alcohol.Experiment 13 The Sodium Borohydride Reduction of Benzil and Benzoin. Experiment 14. The Grignard Reaction: The Preparation of 1,1-Diphenylethanol.Experiment 15 The Asymmetric Dihydroxylation of trans-Stilbene.PineneExperiment 16 Some Chemistry of Oxide Experiment 17. A Dehydrogenation/Hydrogenation Reaction.Experiment 18 The Friedel-Crafts Reaction. Experiment 19 Microwave Heating of Organic Compounds.Experiment 20 The Reaction of 1,1-Diphenylethanol on Clay in the Presence of Microwave Radiation.Experiment 21 The Wittig Reaction.Experiment 22 The Suzuki Reaction Experiment 23. The Crossed-Aldol Condensation Experiment 24. Identifying the Structure of an Aldehyde by Qualitative Analysis.Experiment 25 The Benzoin Reaction.Experiment 26 The DielsAlder ReactionExperiment 27 -ß-Unsaturated Carboxylic Acid Derivative.Synthesis of an Experiment 28. The Reaction of 2-Acetylphenyl Benzoate with Potassium Hydroxide.Experiment 29. The

Reaction of 2-Acetylphenyl Benzoate with Potassium Hydroxide. Experiment 30 Synthesis of 1,2,3,4-Tetrahydro-â-Carboline.Experiment 31 Base-Catalyzed Hydrolysis of Nicotinonitrile Using an Anion-Exchange Resin.Experiment 32 Reactions of Salicylamide.Experiment 33 The Hunsdiecker Reaction.Experiment 34 The Investigation of the Mechanism of a Reaction.Experiment 35 Monoterpenes and the Ritter Reaction.Experiment 36. Chemoselectivity in Transfer-Hydrogenation Reactions. 2011, 526pp, Paperback, 9781111428174 www.cengageasiacom Source: http://www.doksinet assisting conceptual learning. • Critical Thinking Questions appear after each Model and ask students to explore the ideas presented in a number of ways, including drawing a molecule, completing a table, or writing an explanation about a topic to another student who missed class that day. This multi-faceted approach addresses different learning styles, reinforces concepts, and can help reveal areas of weak understanding. •

Exercises following each Model and set of Critical Thinking Questions are matched to certain models presented in the chapter, and test students’ ability to solve problem based on that model. ORGANIC CHEMISTRY, 2E A Guided Inquiry Andrei Straumanis, College of Charleston Designed for use as a supplement to a traditional text to encourage active and collaborative learning in the classroom, this activity book incorporates new methods for teaching chemistry that reflect current research on how students learn. The purpose of the guided inquiry approach is to teach you to think analytically and collaboratively in teams, like scientists do, rather than teaching you to memorize important conclusions arrived at by great scientists of the past. By looking carefully at new problems, constructing logical conclusions based on observations, and discussing the merits of your conclusions with peers, you’ll develop a stronger conceptual understanding of and appreciation for the material. Honing

your logical and empirical skills enables you to better pursue not only chemistry, but any other complex sets of ideas. FEATURES • Unique ChemActivities not found in other texts and study guides consist of a series of Models, Critical Thinking Questions, and Skill Development Exercises that guide student groups in their exploration of organic chemistry. • These materials introduce flexibility into a curriculum, enabling instructors to replace a lecture with group work on a ChemActivity. Students work in small groups while the instructor facilitates and leads whole-class discussions. Students deepen their scientific understanding by explaining topics to one another. • Scientific Models are presented throughout the chapters in bulleted and illustrated formats, CONTENTS Intro Organic Chemistry: a Guided Inquiry.1 Bond Angles and Shape.2 Lewis Structures3 Electron Orbitals.4 Polar Bonds, Polar Reactions5 Resonance.6 Alkanes & Alkenes7 Cycloalkanes8 Addition via Carbocation.9

Addition via Cyclic Intermediate.10 Oxidation and Reduction11 Addition to Alkynes.12 Chirality13 Substitution14 Elimination.15 Radical Reactions16 Synthesis Workshop 1.17 Conjugation and Molecular Orbital (MO) Theory.18 Aromaticity19 EAS: Electrophilic Aromatic Substitution.20 Acidity and pKa of Phenols.21 NAS: Nucleophilic Aromatic Substitution.22 Synthesis Workshop 223 Addition to a Carbonyl.24 Carboxylic Acids & Derivatives25 Enolate & Enol Nucleophiles.26 Aldol and Claisen Reactions.27 AminesSummary of Synthetic Transformations.IndexTable of pKa Values by Structure. 2009, 528pp, Paperback, 9780618974122 www.cengageasiacom 135 Source: http://www.doksinet • • • CTE ORGANIC CHEMISTRY WITH BIOLOGICAL APPLICATIONS WITH CB COURSESMART EBOOK, 3E John E. McMurry, Cornell University • Please note that the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has

arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies.Renowned for its studentfriendly writing style and fresh perspective, this fully updated Third Edition of John McMurry’s ORGANIC CHEMISTRY WITH BIOLOGICAL APPLICATIONS provides full coverage of the foundations of organic chemistry--enhanced by biological examples throughout. In addition, McMurry discusses the organic chemistry behind biological pathways. New problems, illustrations, and essays have been added. Media integration with OWL for Organic Chemistry, a customizable online learning system and assessment tool, reduces faculty workload, facilitates instruction, and helps students master concepts through tutorials, simulations, and algorithmically-generated homework questions. • NEW TO THIS EDITION • WHY THIS CHAPTER? now begins each chapter; it is a brief introduction about the material being covered, why it is important and

how the organic chemistry in the chapter relates to biological chemistry. • Figure and table references in the text are now in color to help reference them. All figure legends 136 now begin with a boldface title to help students easily identify their content. SOMETHING EXTRA essays end each chapter and tie the chapter content to relevant real-world material. Some new essays include, “Organic Foods,” and “Dental Anesthetics.” Many new problems have been included at the end of chapters. Some new content includes: Mercury-catalyzed alkyne hydration (Chapter 8); Enols and tautomerization (Chapter 8); Conversion of alcohols to alkyl fluorides (Chapter 12); Organic coupling reactions (Chapter 12); Base-induced epoxide cleavage (Chapter 13); Killiani-Fischer and Whol degradation (Chapter 21); Prostaglandins and other eicosanoids (Chapter 23). An increase in the number of Organic OWL questions for the online homework system. The #1 online homework and learning system for chemistry,

OWLv2, is available for this text-now with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader™, a new eBook with apps and embedded video. OWLv2 courses for Gen Chem, GOB, Organic, and Liberal Arts now include Quick Prep essential skills assignments that can be taken before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the endof-chapter questions from the text and new iPadcompatible visualizations and tutorials. CONTENTS 1. Structure and Bonding2 Polar Covalent Bonds; Acids and Bases.3 Organic Compounds: Alkanes and Their

Stereochemistry.4 Organic Compounds: Cycloalkanes and Their Stereochemistry.5 Stereochemistry at Tetrahedral Centers.6 An Overview of Organic Reactions.7 Alkenes and Alkynes.8 Reactions of Alkenes and Alkynes9 Aromatic Compounds.10 Structure Determination: www.cengageasiacom Source: http://www.doksinet Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet Spectroscopy.11 Structure Determination: Nuclear Magnetic Resonance Spectroscopy.12 Organohalides: Nucleophilic Substitutions and Eliminations.13 Alcohols, Phenols, and Thiols; Ethers and Sulfides: A Preview of Carbonyl Chemistry 14. Aldehydes and Ketones: Nucleophilic Addition Reactions.15 Carboxylic Acids and Nitriles.16 Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions.17 Carbonyl AlphaSubstitution and Condensation Reactions18 Amines and Heterocycles.19 Biomolecules: Amino Acids, Peptides, and Proteins.20 Amino Acid Metabolism.21 Biomolecules: Carbohydrates22 Carbohydrate Metabolism.23 Biomolecules:

Lipids and Their Metabolism.24 Biomolecules: Nucleic Acids and Their Metabolism.e25 Secondary Metabolites: An Introduction to Natural Products Chemistry.e26 Orbitals and Organic Chemistry: Pericyclic Reactions.e27 Synthetic Polymers 2015, 816pp, Paperback, 9789814624886 CTE ORGANIC CHEMISTRY WITH CB COURSESMART EBOOK, 7E William H. Brown, Beloit College; Brent L Iverson, University of Texas, Austin; Eric Anslyn, University of Texas at Austin; Christopher S. Foote, University of California, Los Angeles Please note that the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies.Succeed in the course with this student-friendly, proven text. Designed throughout to help you master key concepts and improve your problem-solving skills,

CHEMISTRY, Seventh Edition includes a running margin glossary, end-of-chapter in-text mini study guides, a focus on “how to” skills, and more in-chapter examples and problems than any text on the market. To help you understand reaction mechanisms, the authors offset them in a stepwise fashion and emphasize similarities between related mechanisms using just four different characteristics: breaking a bond, making a new bond, adding a proton, and taking a proton away. Thoroughly updated throughout, the book offers numerous biological examples for premed students, unique roadmap problems, a wide range of in-text learning tools, and integration with an online homework and tutorial system, which now includes an interactive multimedia eBook. NEW TO THIS EDITION • MCAT PROBLEMS: To better prepare students for the upcoming new MCAT exam, the new edition includes MCAT PRACTICE: PASSAGE AND www.cengageasiacom 137 Source: http://www.doksinet • • • • PROBLEMS throughout the

text. First students read the organic chemistry-related essay and then answer a series of multiple-choice questions. NEW PRIMERS: Two new primers (Developing a Reaction Mechanism before Chapter 6 and Carboxylic Acid Derivative Reaction Mechanisms before Chapter 18) set key and possibly difficult concepts apart for easy reference to enhance student understanding. NEWLY-DRAWN ORGANIC CHEMISTRY REACTION ROADMAPS: Creating a cumulative, graphical representation of the different reactions students encounter in the context of important functional groups, the organic chemistry roadmaps help students visualize how to interconvert different functional groups (which often require different reactions from different chapters) by simply identifying the most direct path on the roadmap. New pull‐out cards show the roadmaps in sequential order. REVISED REACTION ROADMAP PROBLEMS: These unique problems relate to the authors’ organic chemistry roadmap (see above), which compares organic chemistry to

a roadmap, with functional groups analogous to cities and reactions analogous to the roads between them. FIVE NEW “HOW TO” BOXES: Integrated throughout the text at strategic points, the new boxes show students: “How To: Quickly Figure Out Formal Charge,” “How To: Quickly Recognize the Hybridization and Geometry of Atoms,” “How To: Quickly Draw and Recognize Enantiomers and Diastereomers,” “How To: Retrosynthetically Dissect an Amine into the Proper Starting Materials for a Reductive Amination,” and “How To: Recognize Aromatic Compounds: Criteria and Caveats.” Spectrometry.15 Introduction to Organometallic Compounds.16 Aldehydes and Ketones17 Carboxylic Acids.Primer II: Carboxylic Acid Derivative Reaction Mechanisms.18 Functional Derivatives of Carboxylic Acids.19 Enolate Anions and Enamines.20 Dienes, Conjugated Systems, and Pericyclic Reactions.21 Benzene and the Concept of Aromaticity.22 Reactions of Benzene and Its Derivatives.23 Amines24 Catalytic Carbon–

Carbon Bond Formation.25 Carbohydrates26: Lipids.27 Amino Acids and Proteins28 Nucleic Acids.29 Organic Polymer ChemistryAppendices:1 Thermodynamics and the Equilibrium Constant.2 Major Classes of Organic Acids.3 Bond Dissociation Enthalpies.4 Characteristic 1H-NMR Chemical Shifts.5 Characteristic 13C Chemical Shifts6 Characteristic IR Absorption Frequencies.7 Electrostatic Potential Maps.8 Summary of Stereochemical Terms.9 Summary of the Rules of Nomenclature.10 Common Mistakes in Arrow Pushing.11 Organic Chemistry Roadmaps GLOSSARY G-1.INDEX I-1 2014, 920pp, Paperback, 9789814617833 CONTENTS 1. Covalent Bonding and Shapes of Molecules2 Alkanes and Cycloalkanes.3 Stereochemistry and Chirality.4 Acids and Bases5 AlkenesPrimer I: Reaction Mechanisms6. Reactions of Alkenes7 Alkynes.8 Haloalkanes, Halogenation, and Radical Reactions.9 Nucleophilic Substitution and B-Elimination.10 Alcohols11 Ethers, Sulfides, and Epoxides.12 Infrared Spectroscopy13 Nuclear Magnetic Resonance

Spectroscopy.14 Mass 138 www.cengageasiacom Source: http://www.doksinet PHYSICAL CHEMISTRY reinforces students’ conceptual understanding. • New two-column in-text examples, where appropriate, provide students with more explanation on how to work problems and apply key concepts. • An increased number of end-of-chapter problems provide a wider variety of difficulty. • A stronger thermochemistry presence appears throughout the entire book, not just in Chapters 1-8. FEATURES CTE PHYSICAL CHEMISTRY WITH CB COURSESMART EBOOK, 2E David W. Ball, Cleveland State University Please note that the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies.With its easy-toread approach and focus on core topics, PHYSICAL CHEMISTRY, 2e

provides a concise, yet thorough examination of calculus-based physical chemistry. The Second Edition, designed as a learning tool for students who want to learn physical chemistry in a functional and relevant way, follows a traditional organization and now features an increased focus on thermochemistry, as well as new problems, new two-column examples, and a dynamic new four-color design. Written by a dedicated chemical educator and researcher, the text also includes a review of calculus applications as applied to physical chemistry. NEW TO THIS EDITION • Chapters 1-8 have been completely revised for a better examination of the principles of thermochemistry. • Design and art have been upgraded from a static 2-color display to a dynamic 4-color design. This edition’s dynamic, four-color art and photo program fully complements the text and visually • Chapter 9, “Pre-Quantum Mechanics,” a unique preview to Quantum Mechanics, allows students to develop a better understanding

of the importance, conclusions, and necessity of the subject by putting the state of classical science into a historical context. CONTENTS 1. Gases and the Zeroth Law of Thermodynamics2 The First Law of Thermodynamics.3 The Second and Third Laws of Thermodynamics.4 Free Energy and Chemical Potential.5 Introduction to Chemical Equilibrium.6 Equilibria in SingleComponent Systems7 Equilibria in MultipleComponent Systems8 Electrochemistry and Ionic Solutions.9 Pre-Quantum Mechanics10 Introduction to Quantum Mechanics.11 Quantum Mechanics: Model Systems and the Hydrogen Atom.12 Atoms and Molecules13 Introduction to Symmetry in Quantum Mechanics.14 Rotational and Vibrational Spectroscopy.15 Introduction to Electronic Spectroscopy and Structure.16 Introduction to Magnetic Spectroscopy.17 Statistical Thermodynamics: Introduction.18 More Statistical Thermodynamics.19 The Kinetic Theory of Gases.20 Kinetics21 The Solid State: Crystals.22 SurfacesAppendixesAnswers to Selected Exercises.Index

2015, 576pp, Paperback, 9789814624015 www.cengageasiacom 139 Source: http://www.doksinet NEW TO THIS EDITION SPECTROSCOPY • NEWEST SPECTRA TECHNIQUES: You can easily provide students with the latest spectra techniques, found in Appendix 10, “Index of Spectra”. FEATURES CTE INTRODUCTION TO SPECTROSCOPY WITH CB COURSESMART EBOOK, 5E Donald L. Pavia, Western Washington University; Gary M Lampman, Western Washington University; George S. Kriz, Western Washington University; James A. Vyvyan, Western Washington University Please note that the digital access code that comes with the print book is valid for use in a specific Asia territory only.CB CourseSmart eBook – The ultimate eBook experience has arrived! Easily access our eBooks with features that will improve your reading experience, and tools to help you take notes and organize your studies.Gain an understanding of the latest advances in spectroscopy with INTRODUCTION TO SPECTROSCOPY. This proven book provides a

systematic introduction to spectra and basic theoretical concepts in spectroscopic methods and includes up-to-date spectra; a modern presentation of one-dimensional nuclear magnetic resonance (NMR) spectroscopy; an introduction to biological molecules in mass spectrometry; and coverage of modern techniques alongside DEPT, COSY, and HECTOR. 140 • A TRUSTED, PROVEN RESOURCE: For more than 30 years, this text has proven to be an excellent resource for spectroscopy students and those seeking a solid introductory reference text on spectroscopy. • MODERN COVERAGE: The book provides a modern presentation on one-dimensional NMR spectroscopy. • DETAILED COVERAGE: The mass spectrometry material in Chapter 8 provides a detailed look at biological molecules for the latest coverage on this important topic. • NEWEST SPECTRA TECHNIQUES: The latest spectra techniques are provided in Appendix 10, “Index of Spectra”. • UP-TO-DATE SPECTROGRAPHS: Throughout the text, spectrographs are

created with the latest techniques to ensure accuracy. CONTENTS 1. Molecular Formulas and What Can Be Learned from Them.2 Infrared Spectroscopy3 Nuclear Magnetic Resonance Spectroscopy Part One: Basic Concepts.4 Nuclear Magnetic Resonance Spectroscopy Part Two: Carbon-13 Spectra, Including Heteronuclear Coupling with Other Nuclei.5 Nuclear Magnetic Resonance Spectroscopy Part Three: Spin-Spin Coupling.6 Nuclear Magnetic Resonance Spectroscopy Part Four: Other Topics in One-Dimensional NMR.7 Ultraviolet Spectroscopy.8 Mass Spectrometry9 Combined Structure Problems.10 Nuclear Magnetic Resonance Spectroscopy Part Five: Advanced NMR Techniques.Answers to Selected ProblemsAppendix 1: Infrared Absorption Frequencies of Functional Groups.Appendix 2: Some Representative Chemical Shift Values for Various Types of Protons.Appendix 3: Typical Proton Coupling Constants.Appendix 4: Calculation of Proton (1H) Chemical Shifts. Appendix 5: Calculation of Carbon-13 Chemical Shifts.Appendix 6: 13C

Coupling Constants www.cengageasiacom Source: http://www.doksinet Appendix 7: Tables of Precise Masses and Isotopic Abundance Ratios for Molecular Ions Under Mass 100 Containing Carbon, Hydrogen, Nitrogen, and Oxygen.Appendix 8: Common Fragment Ions Under Mass 105.Appendix 9: Handy-Dandy Guide to Mass Spectral Fragmentation Patterns.Appendix 10: Index of Spectra. 2015, 504pp, Paperback, 9789814624206 www.cengageasiacom 141 Source: http://www.doksinet Combined Author/Title Index A A Beginner’s Guide to Scientific Method, International Edition, 4e p.78/p95 A Microscale Approach to Organic Laboratory Techniques, International Edition, 5e p.118 Applications of Microsoft® Excel in Analytical Chemistry, 2e p.36 Armstrong, General, Organic, and Biochemistry p.28 Armstrong, General, Organic, and Biochemistry, 2e p.8 Armstrong, General, Organic, and Biochemistry, Hybrid Edition (with OWLv2 24-Months Printed Access Card), 2e p.10 A Small Scale Approach to Organic Laboratory

Techniques, 4e p.106 Atwood, Lab Manual for Zumdahl/Zumdahl’s Chemistry: An Atoms First Approach, 2nd, 2e p.59 Atwood, Survival Guide for General Chemistry with Math Review, 2e p.86/p103 Atwood, Survival Guide for Introductory Chemistry p.102 B Ball, CTE Physical Chemistry with CB CourseSmart eBook, 2e p.139 Basic Laboratory Experiments for General, Organic, and Biochemistry p.28 Basic Laboratory Experiments for General, Organic, and Biochemistry, 2e p.7 Bauer/Birk/Sawyer, Laboratory Inquiry in Chemistry, 3e p.85 Bettelheim/Brown/Campbell/Farrell, Introduction to General, Organic and Biochemistry, 11e p.5 Bettelheim/Brown/Campbell/Farrell, Introduction to General, Organic and Biochemistry, International Edition, 10e p.25 Bettelheim/Landesberg, Laboratory Experiments for Introduction to General, Organic and Biochemistry, International Edition, 8e p.26 Biochemistry, International Edition, 5e p.38 Boikess, Chemical Principles for Organic Chemistry p.112 Brown/Holme, CTE Chemistry for

Engineering Students with CB CourseSmart eBook, 3e p.42 Brown/Iverson/Anslyn/Foote, CTE Organic Chemistry with CB CourseSmart eBook, 7e p.114/p138 Brown/Iverson/Anslyn/Foote, Organic Chemistry, Hybrid Edition (with OWLv2 24-Months Printed Access Card), 7e p.116 C Campbell/Farrell, CTE Biochemistry with CB CourseSmart eBook, 8e p.40 Carey, A Beginner’s Guide to Scientific Method, International Edition, 4e p.78/p95 Chem p.105 Chem 2, 2e p.104 Chemical Principles for Organic Chemistry p.112 Chemistry p.79 Chemistry, 2e p.57 Chemistry, 3e p.82 Chemistry, 5e p.64/p66 142 Chemistry, 7e p.81 Chemistry, 8e p.58 Chemistry, 9e p.71 Chemistry & Chemical Reactivity, Hybrid Edition (with OWLv2 24-Months Printed Access Card), 9e p.67 Chemistry for Today, 8e p.13/p14 Chemistry, Hybrid Edition (with OWLv2 24-Months Printed Access Card), 9e p.74 Chemistry, Hybrid Edition (with OWLv2 24-Months Printed Access Card), 10e p.72 Cracolice/Peters, Introductory Chemistry, 5e p.93 Cracolice/Peters,

Introductory Chemistry, Hybrid Edition (with OWLv2 Printed Access Card), 6e p.88 CTE Biochemistry with CB CourseSmart eBook, 8e p.40 CTE Chemical Principles with CB CourseSmart eBook, 7e p.54 CTE Chemistry and Chemical Reactivity with CB CourseSmart eBook, 9e p.50/p55 CTE Chemistry for Engineering Students with CB CourseSmart eBook, 3e p.42 CTE Chemistry with CB CourseSmart eBook, 9e p.43 CTE Chemistry with CB CourseSmart eBook, 10e p.48 CTE Fundamentals of Analytical Chemistry with CB CourseSmart eBook, 9e p.37 CTE General Chemistry with CB CourseSmart eBook, 10e p.47 CTE Introduction to Spectroscopy with CB CourseSmart eBook, 5e p.140 CTE Organic Chemistry with Biological Applications with CB CourseSmart eBook, 3e p.136 CTE Organic Chemistry with CB CourseSmart eBook, 7e p.114/p138 CTE Physical Chemistry with CB CourseSmart eBook, 2e p.139 D Descriptive Inorganic, Coordination, and Solid State Chemistry, 3e p.87 E Ebbing/Gammon, CTE General Chemistry with CB CourseSmart eBook, 10e

p.47 Engel/Kriz/Lampman/Pavia, Introduction to Organic Laboratory Techniques, 3e p.129 Experimental Organic Chemistry, 5e p.127 Experimental Organic Chemistry, 6e p.109 Experiments in General Chemistry, 2e p.84 Experiments in General Chemistry, 6e p.69 Experiments in General Chemistry: Inquiry and Skill Building, 2e p.76 Experiments in General Chemistry, Lab Manual, 10e p.78 F Fundamentals of Organic Chemistry, International Edition, 7e p.128 G Garrett/Grisham, Biochemistry, International Edition, 5e p.38 www.cengageasiacom Source: http://www.doksinet Combined Author/Title Index General Chemistry (with MindTap Chemistry 24-Months Printed Access Card) p.52 General, Organic, and Biochemistry p.28 General, Organic, and Biochemistry, 2e p.8 General, Organic, and Biochemistry, Hybrid Edition (with OWLv2 24-Months Printed Access Card), 2e p.10 General, Organic, and Biological Chemistry, 7e p.2 General, Organic, and Biological Chemistry, Hybrid (with OWLv2 Quick Prep for General

Chemistry Printed Access Card), 7e p.3 General, Organic, and Biological Chemistry, International Edition, 6e p.20 Gilbert/Martin, Experimental Organic Chemistry, 6e p.109 H Hart/Hadad/Craine/Hart, Organic Chemistry, 13e p.123 Hogg, Chem 2, 2e p.104 Holler/Crouch, Applications of Microsoft® Excel in Analytical Chemistry, 2e p.36 I Introduction to Basic Chemistry, International Edition, 7e p.96 Introduction to Chemical Principles, 7e p.101 Introduction to Chemistry, 7e p.98 Introduction to General, Organic and Biochemistry, 11e p.5 Introduction to General, Organic and Biochemistry, International Edition, 10e p.25 Introduction to Organic Laboratory Techniques, 3e p.129 Introductory Chemistry, 5e p.93 Introductory Chemistry, 8e p.90/p91 Introductory Chemistry for Today, International Edition, 7e p.31 Introductory Chemistry for Today, International Edition, 8e p.16 Introductory Chemistry, Hybrid Edition (with OWLv2 Printed Access Card), 6e p.88 J Joesten/Hogg/Donald R. Neu, Chem p105 K

Kotz/Treichel/Townsend/Treichel, Chemistry & Chemical Reactivity, Hybrid Edition (with OWLv2 24-Months Printed Access Card), 9e p.67 Kotz/Treichel/Townsend/Treichel, CTE Chemistry and Chemical Reactivity with CB CourseSmart eBook, 9e p.50/p55 L Lab Manual for Stoker’s General, Organic, and Biological Chemistry, 7th, 7e p.6 Lab Manual for Zumdahl/DeCoste’s Introductory Chemistry: A Foundation, 8th, 8e p.93 Lab Manual for Zumdahl/Zumdahl’s Chemistry, 9th, 9e p.77 Lab Manual for Zumdahl/Zumdahl’s Chemistry: An Atoms First Approach, 2nd, 2e p.59 Laboratory Experiments for Introduction to General, Organic and Biochemistry, International Edition, 8e p.26 Laboratory Inquiry in Chemistry, 3e p.85 Landesberg, Basic Laboratory Experiments for General, Organic, and Biochemistry p.28 Landesberg, Basic Laboratory Experiments for General, Organic, and Biochemistry, 2e p.7 Little, Lab Manual for Zumdahl/DeCoste’s Introductory Chemistry: A Foundation, 8th, 8e p.93 M Martin/Gilbert,

Experimental Organic Chemistry, 5e p.127 Masterton/Hurley, Chemistry, 8e p.58 Masterton/Hurley/Neth, Chemistry, 7e p.81 McMurry, CTE Organic Chemistry with Biological Applications with CB CourseSmart eBook, 3e p.136 McMurry, Fundamentals of Organic Chemistry, International Edition, 7e p.128 McMurry, Organic Chemistry, 3e p.113 McMurry, Organic Chemistry, 9e p.110 McMurry, Organic Chemistry, International Edition, 8e p.124 Moore/Stanitski, Chemistry, 5e p.64/p66 Morrison/Atwood/Caughran, Survival Guide for General, Organic and Biochemistry p.35 Murov, Experiments in General Chemistry, 6e p.69 O Organic and Biochemistry for Today, International Edition, 7e p.32 Organic and Biochemistry for Today, International Edition, 8e p.17 Organic Chemistry p.121/p122 Organic Chemistry, 2e p.135 Organic Chemistry, 3e p.113 Organic Chemistry, 9e p.110 Organic Chemistry, 13e p.123 Organic Chemistry, Hybrid Edition (with OWLv2 24-Months Printed Access Card), 7e p.116 Organic Chemistry, International

Edition, 8e p.124 Organic Experiments, 6e p.132 Oxtoby/Gillis/Butler, Principles of Modern Chemistry, 8e p.60 Oxtoby/Gillis/Butler, Principles of Modern Chemistry, Hybrid Edition (with OWLv2 Printed Access Card), 8e p.62 P Pavia/Kriz/Lampman/Engel, A Microscale Approach to Organic Laboratory Techniques, International Edition, 5e p.118 Pavia/Kriz/Lampman/Engel, A Small Scale Approach to Organic Laboratory Techniques, 4e p.106 Pavia/Lampman/Kriz/Vyvyan, CTE Introduction to Spectroscopy with CB CourseSmart eBook, 5e p.140 Pedersen/Myers, Understanding the Principles of Organic Chemistry p.134 Principles of Modern Chemistry, 8e p.60 Principles of Modern Chemistry, Hybrid Edition (with www.cengageasiacom 143 Source: http://www.doksinet Combined Author/Title Index V OWLv2 Printed Access Card), 8e p.62 Pushing Electrons, 4e p.118 R Reger/Goode/Ball, Chemistry, 3e p.82 Rodgers, Descriptive Inorganic, Coordination, and Solid State Chemistry, 3e p.87 Rosen, The Guide to Surviving

General Chemistry, 2e p.53 S Safety-Scale Laboratory Experiments for Chemistry for Today, 7e p.34 Safety-Scale Laboratory Experiments for Chemistry for Today, 8e p.19 Seager/Slabaugh, Chemistry for Today, 8e p.13/p14 Seager/Slabaugh, Introductory Chemistry for Today, International Edition, 7e p.31 Seager/Slabaugh, Introductory Chemistry for Today, International Edition, 8e p.16 Seager/Slabaugh, Organic and Biochemistry for Today, International Edition, 7e p.32 Seager/Slabaugh, Organic and Biochemistry for Today, International Edition, 8e p.17 Seager/Slabaugh, Safety-Scale Laboratory Experiments for Chemistry for Today, 7e p.34 Seager/Slabaugh, Safety-Scale Laboratory Experiments for Chemistry for Today, 8e p.19 Skoog/West/Holler/Crouch, CTE Fundamentals of Analytical Chemistry with CB CourseSmart eBook, 9e p.37 Stanton/Zhu/Atwood, Experiments in General Chemistry, 2e p.84 Stoker, General, Organic, and Biological Chemistry, 7e p.2 Stoker, General, Organic, and Biological Chemistry,

Hybrid (with OWLv2 Quick Prep for General Chemistry Printed Access Card), 7e p.3 Stoker, General, Organic, and Biological Chemistry, International Edition, 6e p.20 Stoker, Lab Manual for Stoker’s General, Organic, and Biological Chemistry, 7th, 7e p.6 Straumanis, Organic Chemistry p.121/p122 Straumanis, Organic Chemistry, 2e p.135 Survival Guide for General Chemistry with Math Review, 2e p.86/p103 Survival Guide for General, Organic and Biochemistry p.35 Survival Guide for Introductory Chemistry p.102 Vining/Young/Day/Botch, General Chemistry (with MindTap Chemistry 24-Months Printed Access Card) p.52 W Weeks, Pushing Electrons, 4e p.118 Weiner/Harrison, Introduction to Chemical Principles, 7e p.101 Wentworth/Munk, Experiments in General Chemistry, Lab Manual, 10e p.78 Whitten/Davis/Peck/Stanley, Chemistry, Hybrid Edition (with OWLv2 24-Months Printed Access Card), 10e p.72 Whitten/Davis/Peck/Stanley, CTE Chemistry with CB CourseSmart eBook, 10e p.48 Williamson/Masters, Organic

Experiments, 6e p.132 Williamson/Masters, Techniques Labs for Macroscale and Microscale Organic Experiments (with CourseMate 2-Semester Printed Access Card), 6e p.126 Williamson/Peck, Experiments in General Chemistry: Inquiry and Skill Building, 2e p.76 Z Zumdahl/DeCoste, CTE Chemical Principles with CB CourseSmart eBook, 7e p.54 Zumdahl/DeCoste, Introduction to Basic Chemistry, International Edition, 7e p.96 Zumdahl/DeCoste, Introduction to Chemistry, 7e p.98 Zumdahl/DeCoste, Introductory Chemistry, 8e p.90/p91 Zumdahl/Zumdahl, Chemistry p.79 Zumdahl/Zumdahl, Chemistry, 2e p.57 Zumdahl/Zumdahl, Chemistry, 9e p.71 Zumdahl/Zumdahl, Chemistry, Hybrid Edition (with OWLv2 24-Months Printed Access Card), 9e p.74 Zumdahl/Zumdahl, CTE Chemistry with CB CourseSmart eBook, 9e p.43 Zumdahl/Zumdahl, Lab Manual for Zumdahl/Zumdahl’s Chemistry, 9th, 9e p.77 T Techniques Labs for Macroscale and Microscale Organic Experiments (with CourseMate 2-Semester Printed Access Card), 6e p.126 The Guide to

Surviving General Chemistry, 2e p.53 U Understanding the Principles of Organic Chemistry p.134 144 www.cengageasiacom Source: http://www.doksinet ORDER FORM / PRICE LIST QTY YEAR ISBN NO. AUTHOR TITLE/EDITION PAGE NO. PRICE(USD) A 2012 9781111726010 Carey A Beginner’s Guide to Scientific Method, International Edition, 4e p.78/p95 89.95 2013 9781133107415 Pavia A Microscale Approach to Organic Laboratory Techniques, International Edition, 5e p.118 341.95 2016 9781305253926 Pavia A Small Scale Approach to Organic Laboratory Techniques, 4e p.106 329.95 2014 9781285087955 Holler Applications of Microsoft® Excel in Analytical Chemistry, 2e p.36 82.95 2012 9781111426613 Landesberg Basic Laboratory Experiments for General, Organic, and Biochemistry p.28 89.95 2015 9781285459653 Landesberg Basic Laboratory Experiments for General, Organic, and Biochemistry, 2e p.7 89.95 2013 9781133108795 Garrett Biochemistry,

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