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Book
1241, A-17, G-19, C-2, I-34 pages : illustrations (some color) ; 29 cm
Science Library (Li and Ma)
CHEM-35-01, CHEM-35-01, CHEM-35-01, CHEM-35-01
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
Book
vii, 387 pages : illustrations ; 24 cm
  • Chapter 1 Aromaticity 1.1 Introduction to Aromatic Compounds 1.2 Nomenclature of Aromatic Compounds 1.3 Criteria for Aromaticity 1.4 Lone Pairs Chapter 2 IR Spectroscopy 2.1 Vibrational Excitation 2.2 IR Spectra 2.3 Wavenumber 2.4 Signal Intensity 2.5 Signal Shape 2.6 Analyzing an IR Spectrum Chapter 3 NMR Spectroscopy 3.1 Chemical Equivalence 3.2 Chemical Shift (Benchmark Values) 3.3 Integration 3.4 Multiplicity 3.5 Pattern Recognition 3.6 Complex Splitting 3.7 No Splitting 3.8 Hydrogen Deficiency Index (Degrees of Unsaturation) 3.9 Analyzing a Proton NMR Spectrum 3.10 13C NMR Spectroscopy Chapter 4 Electrophilic Aromatic Substitution 4.1 Halogenation and the Role of Lewis Acids 4.2 Nitration 4.3 Friedel-Crafts Alkylation and Acylation 4.4 Sulfonation 4.5 Activation and Deactivation 4.6 Directing Effects 4.7 Identifying Activators and Deactivators 4.8 Predicting and Exploiting Steric Effects 4.9 Synthesis Strategies Chapter 5 Nucleophilic Aromatic Substitution 5.1 Criteria for Nucleophilic Aromatic Substitution 5.2 SNAr Mechanism 5.3 Elimination-Addition 5.4 Mechanism Strategies Chapter 6 Ketones and Aldehydes 6.1 Preparation of Ketones and Aldehydes 6.2 Stability and Reactivity of CO Bonds 6.3 H-Nucleophiles 6.4 O-Nucleophiles 6.5 S-Nucleophiles 6.6 N-Nucleophiles 6.7 C-Nucleophiles 6.8 Some Important Exceptions to the Rule 6.9 How to Approach Synthesis Problems Chapter 7 Carboxylic Acid Derivatives 7.1 Reactivity of Carboxylic Acid Derivatives 7.2 General Rules 7.3 Acid Halides 7.4 Acid Anhydrides 7.5 Esters 7.6 Amides and Nitriles 7.7 Synthesis Problems Chapter 8 Enols and Enolates 8.1 Alpha Protons 8.2 Keto-Enol Tautomerism 8.3 Reactions Involving Enols 8.4 Making Enolates 8.5 Haloform Reaction 8.6 Alkylation of Enolates 8.7 Aldol Reactions 8.8 Claisen Condensation 8.9 Decarboxylation 8.10 Michael Reactions Chapter 9 Amines 9.1 Nucleophilicity and Basicity of Amines 9.2 Preparation of Amines through SN2 Reactions 9.3 Preparation of Amines through Reductive Amination 9.4 Acylation of Amines 9.5 Reactions of Amines with Nitrous Acid 9.6 Aromatic Diazonium Salts Chapter 10 Diels-Alder Reactions 10.1 Introduction and Mechanism 10.2 The Dienophile 10.3 The Diene 10.4 Other Pericyclic Reactions Answer Key Index.
  • (source: Nielsen Book Data)9781119110651 20160704
Readers continue to turn to Klein's Organic Chemistry As a Second Language: Second Semester Topics, 4th Edition because it enables them to better understand fundamental principles, solve problems, and focus on what they need to know to succeed. The fourth edition explores the major principles in the field and explains why they are relevant. It is written in a way that clearly shows the patterns in organic chemistry so that readers can gain a deeper conceptual understanding of the material. Topics are presented clearly in an accessible writing style along with numerous hands-on problem solving exercises.
(source: Nielsen Book Data)9781119110651 20160704
Science Library (Li and Ma)
CHEM-35-01

4. 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
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
1270 p. : ill. (chiefly col.) ; 29 cm.
  • Preface Structure and Bonding in Organic Molecules Structure and Reactivity: Acids and Bases, Polar and Nonpolar Molecules Reactions of Alkanes: Bond-Dissociation Energies, Radical Halogenation, and Relative Reactivity Cycloalkanes Stereoisomers Properties and Reactions of Haloalkanes: Bimolecular Nucleophilic Substitution Further Reactions of Haloalkanes: Unimolecular Substitution and Pathways of Elimination Hydroxy Functional Group: Alcohols: Properties, Preparation, and Strategy of Synthesis Further Reactions of Alcohols and the Chemistry of Ethers Using Nuclear Magnetic Resonance Spectroscopy to Deduce Structure Alkenes-- Infrared Spectroscopy and Mass Spectrometry Reactions of Alkenes Alkynes: The Carbon-Carbon Triple Bond Delocalized Pi Systems: Investigation by Ultraviolet and Visible Spectroscopy Benzene and Aromaticity: Electrophilic Aromatic Substitution Electrophilic Attack on Derivatives of Benzene: Substituents Control Regioselectivity Aldehydes and Ketones: The Carbonyl Group Enols, Enolates and the Aldol Condensation: I , beta-Unsaturated Aldehydes and Ketones Carboxylic Acids Carboxylic Acid Derivatives Amines and Their Derivatives: Functional Groups Containing Nitrogen Chemistry of Benzene Substituents: Alkylbenzenes, Phenols, and Benzenamines Ester Enolates and the Claisen Condensation: Synthesis of beta-Dicarbonyl Compounds-- Acyl Anion Equivalents Carbohydrates: Polyfunctional Compounds in Nature Heterocycles: Heteroatoms in Cyclic Organic Compounds Amino Acids, Peptides, Proteins, and Nucleic Acids: Nitrogen-Containing Polymers in Nature MCAT Questions Answers to Exercises Photograph Credits Index.
  • (source: Nielsen Book Data)9781429239240 20160604
With authors who are both accomplished researchers and educators, Vollhardt and Schore's Organic Chemistry has proven effective for making contemporary organic chemistry accessible, introducing cutting-edge research in a fresh, student-friendly way. A wealth of unique study tools help students organize and understand the substantial information presented in this course. In the sixth edition, the themes of understanding reactivity, mechanisms, and synthetic analysis to apply chemical concepts to realistic situations has been strengthened. New applications of organic chemistry in the life sciences, industrial practices, green chemistry, and environmental monitoring and clean-up are incorporated to keep the book up to date on these increasingly important topics. The book is supported by a companion website (www.whfreeman.com/vollhardtschore6e), which offers students a range of tools for problem-solving and chemical exploration, including molecular modelling questions, online quizzes, animations, and lecture videos from Peter Vollhardt.
(source: Nielsen Book Data)9781429239240 20160604
Science Library (Li and Ma)
CHEM-35-01, CHEM-35-01, CHEM-35-01, CHEM-35-01
Book
x, 519 p. : ill. ; 28 cm.
  • Works alongside the content of the main text (ISBN 978-1-4292-3924-0).
  • (source: Nielsen Book Data)9781429231367 20160605
The study guide provides extra study support for students using Organic Chemistry, sixth edition, by Vollhardt and Schore. It contains chapter outlines, detailed comments and new material for each section, a full glossary and reasoned solutions to the end-of-chapter questions.
(source: Nielsen Book Data)9781429231367 20160605
Science Library (Li and Ma)
CHEM-35-01, CHEM-35-01, CHEM-35-01, CHEM-35-01