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Book
xii, 382 pages : illustrations ; 24 cm
  • CHAPTER 1 BOND-LINE DRAWINGS 1 1.1 How to Read Bond-Line Drawings 1 1.2 How to Draw Bond-Line Drawings 5 1.3 Mistakes to Avoid 7 1.4 More Exercises 7 1.5 Identifying Formal Charges 9 1.6 Finding Lone Pairs that are Not Drawn 13 CHAPTER 2 RESONANCE 18 2.1 What is Resonance? 18 2.2 Curved Arrows: The Tools for Drawing Resonance Structures 19 2.3 The Two Commandments 21 2.4 Drawing Good Arrows 24 2.5 Formal Charges in Resonance Structures 26 2.6 Drawing Resonance Structures Step by Step 30 2.7 Drawing Resonance Structures by Recognizing Patterns 34 2.8 Assessing the Relative Importance of Resonance Structures 43 CHAPTER 3 ACID BASE REACTIONS 49 3.1 Factor 1 What Atom is the Charge On? 50 3.2 Factor 2 Resonance 53 3.3 Factor 3 Induction 56 3.4 Factor 4 Orbitals 59 3.5 Ranking the Four Factors 60 3.6 Other Factors 63 3.7 Quantitative Measurement (pKa Values) 64 3.8 Predicting the Position of Equilibrium 65 3.9 Showing a Mechanism 66 CHAPTER 4 GEOMETRY 69 4.1 Orbitals and Hybridization States 69 4.2 Geometry 72 4.3 Lone Pairs 76 CHAPTER 5 NOMENCLATURE 77 5.1 Functional Group 78 5.2 Unsaturation 80 5.3 Naming the Parent Chain 81 5.4 Naming Substituents 84 5.5 Stereoisomerism 88 5.6 Numbering 90 5.7 Common Names 95 5.8 Going from a Name to a Structure 96 CHAPTER 6 CONFORMATIONS 97 6.1 How to Draw a Newman Projection 98 6.2 Ranking the Stability of Newman Projections 102 6.3 Drawing Chair Conformations 105 6.4 Placing Groups On the Chair 108 6.5 Ring Flipping 112 6.6 Comparing the Stability of Chairs 119 6.7 Don t Be Confused by the Nomenclature 122 CHAPTER 7 CONFIGURATIONS 123 7.1 Locating Stereocenters 123 7.2 Determining the Configuration of a Stereocenter 126 7.3 Nomenclature 134 7.4 Drawing Enantiomers 138 7.5 Diastereomers 143 7.6 Meso Compounds 144 7.7 Drawing Fischer Projections 147 7.8 Optical Activity 152 CHAPTER 8 MECHANISMS 154 8.1 Introduction to Mechanisms 154 8.2 Nucleophiles and Electrophiles 154 8.3 Basicity vs. Nucleophilicity 157 8.4 Arrow-Pushing Patterns for Ionic Mechanisms 159 8.5 Carbocation Rearrangements 164 8.6 Information Contained in a Mechanism 169 CHAPTER 9 SUBSTITUTION REACTIONS 173 9.1 The Mechanisms 173 9.2 Factor 1 The Electrophile (Substrate) 175 9.3 Factor 2 The Nucleophile 178 9.4 Factor 3 The Leaving Group 180 9.5 Factor 4 The Solvent 183 9.6 Using All Four Factors 185 9.7 Substitution Reactions Teach Us Some Important Lessons 186 CHAPTER 10 ELIMINATION REACTIONS 188 10.1 The E2 Mechanism 188 10.2 The Regiochemical Outcome of an E2 Reaction 189 10.3 The Stereochemical Outcome of an E2 Reaction 191 10.4 The E1 Mechanism 194 10.5 The Regiochemical Outcome of an E1 Reaction 195 10.6 The Stereochemical Outcome of an E1 Reaction 196 10.7 Substitution vs. Elimination 196 10.8 Determining the Function of the Reagent 197 10.9 Identifying the Mechanism(s) 199 10.10 Predicting the Products 202 CHAPTER 11 ADDITION REACTIONS 206 11.1 Terminology Describing Regiochemistry 206 11.2 Terminology Describing Stereochemistry 208 11.3 Adding H and H 216 11.4 Adding H and X, Markovnikov 219 11.5 Adding H and Br, Anti-Markovnikov 226 11.6 Adding H and OH, Markovnikov 230 11.7 Adding H and OH, Anti-Markovnikov 233 11.8 Synthesis Techniques 238 11.9 Adding Br and Br-- Adding Br and OH 245 11.10 Adding OH and OH, ANTI 250 11.11 Adding OH and OH, SYN 253 11.12 Oxidative Cleavage of an Alkene 255 CHAPTER 12 ALKYNES 258 12.1 Structure and Properties of Alkynes 258 12.2 Preparation of Alkynes 261 12.3 Alkylation of Terminal Alkynes 262 12.4 Reduction of Alkynes 264 12.5 Hydration of Alkynes 268 12.6 Keto-Enol Tautomerization 273 12.7 Ozonolysis of Alkynes 278 CHAPTER 13 ALCOHOLS 280 13.1 Naming and Designating Alcohols 280 13.2 Predicting Solubility of Alcohols 281 13.3 Predicting Relative Acidity of Alcohols 283 13.4 Preparing Alcohols: A Review 286 13.5 Preparing Alcohols via Reduction 287 13.6 Preparing Alcohols via Grignard Reactions 294 13.7 Summary of Methods for Preparing Alcohols 298 13.8 Reactions of Alcohols: Substitution and Elimination 300 13.9 Reactions of Alcohols: Oxidation 303 13.10 Converting an Alcohol Into an Ether 305 CHAPTER 14 ETHERS AND EPOXIDES 308 14.1 Introduction to Ethers 308 14.2 Preparation of Ethers 310 14.3 Reactions of Ethers 313 14.4 Preparation of Epoxides 314 14.5 Ring-Opening Reactions of Epoxides 316 CHAPTER 15 SYNTHESIS 323 15.1 One-Step Syntheses 324 15.2 Multistep Syntheses 336 15.3 Retrosynthetic Analysis 337 15.4 Creating Your Own Problems 338 Answer Key 339 Index 000.
  • (source: Nielsen Book Data)9781119110668 20160704
* Helps develop the skills needed to solve a variety of problem types. * Presents the fundamental topics clearly with an informal, friendly tone. * Describes the how-to of problem solving, including approaching problems strategically. * Discusses the relationship between concepts and puts topics in context. * Covers important areas such as resonance, nomenclature, conformations, substitution reactions, synthesis and more.
(source: Nielsen Book Data)9781119110668 20160704
Science Library (Li and Ma)
CHEM-33-01, CHEM-33-01, CHEM-33-01, CHEM-33C-01, CHEM-35-01, CHEM-35-01, CHEM-35-01, CHEM-35-01

2. Organic chemistry [2016]

Book
xxx, 1054, 59, 34 pages : illustrations ; 26 cm
  • 1. Structure and Bonding. 2. 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. Practice Your Scientific Analysis and Reasoning I: The Chiral Drug Thalidomide 8. Alkenes: Reactions and Synthesis. 9. 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 Mustard Gas to Alkylating Anticancer Drugs 12. 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 Alpha-Substitution Reactions. 23. Carbonyl Condensation Reactions. Practice Your Scientific Analysis and Reasoning V: Thymine in DNA 24. Amines and Heterocycles. 25. Biomolecules: Carbohydrates. 26. Biomolecules: Amino Acids, Peptides, and Proteins. Practice Your Scientific Analysis and Reasoning VI: Melatonin and Serotonin 27. Biomolecules: Lipids. 28. 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.
  • (source: Nielsen Book Data)9781305080485 20160618
Master organic chemistry with the help of this proven best-seller! John McMurry's Organic Chemistry is consistently praised as the most clearly written book available for the course. In John McMurry's words: "I wrote this book because I love writing. I get great pleasure and satisfaction from taking a complicated subject, turning it around until I see it clearly from a new angle, and then explaining it in simple words." Through his lucid writing and ability to show the beauty and logic of organic chemistry, McMurry makes learning enjoyable. The highest compliment that can be given to a chemistry book applies to McMurry: It works!.
(source: Nielsen Book Data)9781305080485 20160618
Science Library (Li and Ma)
CHEM-33-01, CHEM-33-01, CHEM-33-01, CHEM-33C-01
Book
vi, 1116, [1] pages : illustrations ; 28 cm
Science Library (Li and Ma)
CHEM-33-01, CHEM-33-01, CHEM-33-01, CHEM-33C-01

4. Organic chemistry [2014]

Book
1 v. (various pagings) : ill. (some col.) ; 29 cm
  • Preface Prologue Chapter 1 Structure and Bonding Chapter 2 Acids and Bases Chapter 3 Introduction to Organic Molecules and Functional Groups Chapter 4 Alkanes Chapter 5 Stereochemistry Chapter 6 Understanding Organic Reactions Chapter 7 Alkyl Halides and Nucleophilic Substitution Chapter 8 Alkyl Halides and Elimination Reactions Chapter 9 Alcohols, Ethers, and Epoxides Chapter 10 Alkenes Chapter 11 Alkynes Chapter 12 Oxidation and Reduction Chapter 13 Mass Spectrometry and Infrared Spectroscopy Chapter 14 Nuclear Magnetic Resonance Spectroscopy Chapter 15 Radical Reactions Chapter 16 Conjugation, Resonance, and Dienes Chapter 17 Benzene and Aromatic Compounds Chapter 18 Reactions of Aromatic Compounds Chapter 19 Carboxylic Acids and Acidity of the O-H Bond Chapter 20 Introduction to Carbonyl Chemistry: Organometallic Reagents-- Oxidation and Reduction Chapter 21 Aldehydes and Ketones-Nucleophilic Addition Chapter 22 Carboxylic Acids and Their Derivatives-Nucleophilic Acyl Substitution Chapter 23 Substitution Reactions of Carbonyl Compounds at the a-Carbon Chapter 24 Carbonyl Condensation Reactions Chapter 25 Amines Chapter 26 Carbon-Carbon Bond-Forming Reactions in Organic Synthesis Chapter 27 Pericyclic Reactions Chapter 28 Carbohydrates Chapter 29 Amino Acids and Proteins Chapter 30 Lipids Chapter 31 Synthetic Polymers Appendices Glossary Credits Index.
  • (source: Nielsen Book Data)9789814581882 20160613
Serious Science with an Approach Built for Today's Students Smith's Organic Chemistry continues to breathe new life into the organic chemistry world. This new fourth edition retains its popular delivery of organic chemistry content in a student-friendly format. Janice Smith draws on her extensive teaching background to deliver organic chemistry in a way in which students learn: with limited use of text paragraphs, and through concisely written bulleted lists and highly detailed, well-labeled "teaching" illustrations. Don't make your text decision without seeing Organic Chemistry, 4th edition by Janice Gorzynski Smith!.
(source: Nielsen Book Data)9789814581882 20160613
Science Library (Li and Ma)
CHEM-33-01, CHEM-33-01, CHEM-33-01, CHEM-33C-01

5. Organic chemistry [2015]

Book
xxxvii, 1247 pages : illustrations (chiefly color) ; 29 cm
Written by two expert teachers, the Fifth Edition of Organic Chemistry is written to support all kinds of learners whether students read the book, or use it as a reference. New Visualize, Understand, Draw sections help students draw molecules well, visualize how they are formed, and understand why reactions occur. The Fifth Edition has been revised to be more accessible, with a focus on the basics and more opportunities for problem-solving practice, while the robust media package helps students visualize organic chemistry.".
(source: Nielsen Book Data)9780393913033 20160617
Science Library (Li and Ma)
CHEM-33-01, CHEM-33-01, CHEM-33-01, CHEM-33C-01, CHEM-35-01, CHEM-35-01, CHEM-35-01, CHEM-35-01
Book
xxxiv, 1223, A-58, C-2, I-22 pages : illustrations ; 29 cm
  • 1. Structure and Bonding in Organic Molecules 2. Structure and Reactivity 3. Reactions of Alkanes 4. Cycloalkanes 5. Stereoisomers 6. Properties and Reactions of Haloalkanes 7. Further Reactions of Haloalkanes 8. Hydroxy Functional Group: Alcohols 9. Further Reactions of Alcohols and the Chemistry of Ethers 10. Using Nuclear Magnetic Resonance Spectroscopy to Deduce Structure 11. Alkenes: Infrared Spectroscopy and Mass Spectrometry 12. Reactions of Alkenes 13. Alkynes 14. Delocalized Pi Systems 15. Benzene and Aromaticity 16. Electrophilic Attack on Derivatives of Benzene 17. Aldehydes and Ketones 18. Enols, Enolates and the Aldol Condensation 19. Carboxylic Acids 20. Carboxylic Acid Derivatives 21. Amines and Their Derivatives 22. Chemistry of Benzene Substituents 23. Ester Enolates and the Claisen Condensation 24. Carbohydrates: Polyfunctional Compounds in Nature 25. Heterocycles: Heteroatoms in Cyclic Organic Compounds 26. Amino Acids, Peptides, Proteins, and Nucleic Acids: Nitrogen-Containing Polymers in Nature.
  • (source: Nielsen Book Data)9781464120275 20160618
With authors who are accomplished researchers and educators, Organic Chemistry helps students understand the connection between structure and function to prepare them to understand mechanisms and solve practical problems in organic chemistry. The new edition brings in the latest research breakthroughs and includes expanded problem-solving help.
(source: Nielsen Book Data)9781464120275 20160618
Science Library (Li and Ma)
CHEM-33-01, CHEM-33-01, CHEM-33-01, CHEM-33C-01, CHEM-35-01, CHEM-35-01, CHEM-35-01, CHEM-35-01
Book
1 volume (various pagings) : illustrations ; 28 cm
Science Library (Li and Ma)
CHEM-33-01, CHEM-33-01, CHEM-33-01, CHEM-33C-01
Book
x, 521 pages : illustrations ; 28 cm
  • Preface: A User's Guide to Organic Chemistry: Structure and Function 1. Structure and Bonding in Organic Molecules 2. Structure and Reactivity 3. Reactions of Alkanes 4. Cycloalkanes 5. Stereoisomers 6. Properties and Reactions of Haloalkanes 7. Further Reactions of Haloalkanes 8. Hydroxy Functional Group: Alcohols: Properties, Preparation, and Strategy of Synthesis 9. Further Reactions of Alcohols and the Chemistry of Ethers 10. Using Nuclear Magnetic Resonance Spectroscopy to Deduce Structure 11. Alkenes: Infrared Spectroscopy and Mass Spectrometry 12. Reactions of Alkenes 13. Alkynes 14. Delocalized Pi Systems 15. Benzene and Aromaticity 16. Electrophilic Attack on Derivatives of Benzene 17. Aldehydes and Ketones 18. Enols, Enolates and the Aldol Condensation 19. Carboxylic Acids 20. Carboxylic Acid Derivatives 21. Amines and Their Derivatives 22. Chemistry of Benzene Substituents 23. Ester Enolates and the Claisen Condensation 24. Carbohydrates: Polyfunctional Compounds in Nature 25. Heterocycles: Heteroatoms in Cyclic Organic Compounds 26. Amino Acids, Peptides, Proteins, and Nucleic Acids: Nitrogen-Containing.
  • (source: Nielsen Book Data)9781464162251 20160618
This manual includes chapter introductions that highlight new materials, chapter outlines, detailed comments for each chapter section, a glossary, and solutions to the problems, presented in a way that shows students how to reason their way to the answer.
(source: Nielsen Book Data)9781464162251 20160618
Science Library (Li and Ma)
CHEM-33-01, CHEM-33-01, CHEM-33-01, CHEM-33C-01, CHEM-35-01, CHEM-35-01, CHEM-35-01, CHEM-35-01
Book
vi, 950 pages : ill. ; 28 cm
Science Library (Li and Ma)
CHEM-33-01, CHEM-33-01, CHEM-33-01, CHEM-33C-01, CHEM-35-01, CHEM-35-01, CHEM-35-01, CHEM-35-01
Book
xxiv, 1038, 83, 35 p. : col. ill. ; 26 cm.
  • 1. The Atomic Nature of Matter. 2. Stoichiometry. 3. Chemical Periodicity and the Formation of Simple Compounds. 4. Types of Chemical Reactions. 5. The Gaseous State. 6. Condensed Phases and Phase Transitions. 7. Chemical Equilibrium. 8. Acid?Base Equilibria. 9. Dissolution and Precipitation Equilibria. 10. Thermochemistry. 11. Spontaneous Change and Equilibrium. 12. Redox Reactions and Electrochemistry. 13. Electrochemistry and Cell Voltage. 14. Chemical Kinetics. 15. Nuclear Chemistry. 16. Quantum Mechanics and the Hydrogen Atom. 17. Many-electron Atoms and Chemical Bonding. 18. Molecular Orbitals, Spectroscopy, and Atmospheric Chemistry. 19. Coordination Complexes. 20. Structure and Bonding in Solids. 21. Silicon and Solid-State Materials. 22. Chemical Processes. 23. Chemistry of the Halogens. 24. From Petroleum to Pharmaceuticals. 25. Synthetic and Biological Polymers.
  • (source: Nielsen Book Data)9780030331886 20160528
The organization of the text treats chemistry as an experimental subject by beginning with observable, macroscopic chemistry and later moving to the quantum mechanical theory that provides the underpinning of modern chemistry.
(source: Nielsen Book Data)9780030331886 20160528
Science Library (Li and Ma)
CHEM-33-01, CHEM-33-01, CHEM-33-01, CHEM-33C-01
Book
331 p. : ill. ; 26 cm.
Science Library (Li and Ma)
CHEM-33-01, CHEM-33-01, CHEM-33-01, CHEM-33C-01