Produktbild: Organic Chemistry

Organic Chemistry An Acid-Base Approach, Third Edition

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Beschreibung

Produktdetails

Einband

Taschenbuch

Erscheinungsdatum

09.10.2024

Abbildungen

schwarz-weiss Illustrationen, farbige Illustrationen, Raster, schwarz-weiss, Raster, farbig, Zeichnungen, schwarz-weiss, Zeichnungen, farbig, Tabellen, schwarz-weiss

Verlag

Taylor & Francis

Seitenzahl

694

Maße (L/B/H)

28/21/3,9 cm

Gewicht

1748 g

Auflage

3. Auflage

Sprache

Englisch

ISBN

978-1-03-200616-1

Beschreibung

Produktdetails

Einband

Taschenbuch

Erscheinungsdatum

09.10.2024

Abbildungen

schwarz-weiss Illustrationen, farbige Illustrationen, Raster, schwarz-weiss, Raster, farbig, Zeichnungen, schwarz-weiss, Zeichnungen, farbig, Tabellen, schwarz-weiss

Verlag

Taylor & Francis

Seitenzahl

694

Maße (L/B/H)

28/21/3,9 cm

Gewicht

1748 g

Auflage

3. Auflage

Sprache

Englisch

ISBN

978-1-03-200616-1

Herstelleradresse

Libri GmbH
Europaallee 1
36244 Bad Hersfeld
DE

Email: gpsr@libri.de

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  • Produktbild: Organic Chemistry
  • Chapter 1: Introduction

    1.1. A Brief History of Organic Chemistry

    1.2. The Variety and Beauty of Organic Molecules

    Chapter 2: Why Is an Acid-Base Theme Important?

    2.1. Traditional Acid and Base Theory

    2.2. There are Two Acid-Base Definitions: How Are They Related?

    2.3. Acid-Base Equilibria and Equilibrium Constants

    2.4. Electronegativity and Atom Size

    2.4.A. Electronegativity

    2.4. B. Atom Size

    2.5. Atom Size and Electronegativity Arguments Applied to Acids and Bases

    2.6. Resonance, Electron Dispersion and Base Strength

    2.7. Lewis Acids and Bases

    2.8. Why Is Acid-Base Chemistry a Theme for Organic Chemistry?

    2.9. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 3: Bonding

    3.1. Atomic orbitals and Electrons

    3.1.A. Atomic Orbitals

    3.1.B. Electronic Configuration

    3.2. Ionic versus Covalent Chemical Bonds

    3.3. Covalent Bonds

    3.4. Linear Combination of Atomic Orbital (LCAO) Model

    3.5. Tetrahedral Carbons and sp3 Hybridization

    3.5.A. The Experimentally Determined Structure of Methane

    3.5.B. Electron Promotion and sp3 Hybridization

    3.5.C. The Hybrid Carbon Model of sp3-Hybrid Orbitals

    3.6. The Valence Shell Electron Pair Repulsion (VSEPR) Model

    3.7. Breaking Covalent Bonds

    3.8. Carbon Bonded to Heteroatoms

    3.8.A. A Covalent Bond Between Carbon and a Heteroatom: Bond Polarization

    3.8.B. Bond Polarity, Bond Moments, and Bond Strength

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 4: Alkanes, Isomers, and an Introduction to Nomenclature

    4.1. Alkanes

    4.2. Structural Variations of Alkane Hydrocarbons

    4.2.A. Straight-chain and Branched Alkanes

    4.2.B. Isomers

    4.3. The IUPAC Rules of Nomenclature

    4.3.A. Prefixes and Simple Alkanes

    4.3.B. Common Names

    4.3.C. Halogens are Substituents

    4.3.D. Multiple Substituents

    4.3.E. Complex Substituents

    4.4. Rings Made of Carbon: Cyclic Compounds

    4.5. The Acid or Base Properties of Alkanes

    4.6. Combustion Analysis and Empirical Formulas

    4.7. Commercial and Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 5: Functional Groups

    5.1. -Bonds. The C=C Unit and Alkenes

    5.2. -Bonds. The CºC Unit and Alkynes

    5.3. Hydrocarbons With Several -Bonds

    5.4. Terpenes

    5.5. Heteroatom Functional Groups

    5.5.A. Alcohols and Thiols

    5.5.B. Ethers and Dithioethers (Sulfides)

    5.5.C. Amines

    5.6. Functional Groups With Polarized -Bonds

    5.6.A. The Carbonyl Functional Group, C=O

    5.6.B. Ketones and Aldehydes

    5.6.C. Carboxylic Acids, Carboxylic Anions and Resonance

    5.6.D. Double and Triple Bonds to Nitrogen

    5.7. Acid-Base Properties of Functional Groups

    5.8. Physical Properties and Intermolecular Forces

    5.8.A. Boiling Point

    5.8.B. Solubility

    5.8.C. Melting Point

    5.9. Benzene: A Special Cyclic Hydrocarbon

    5.10. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 6: Acids, Bases, and Nucleophiles

    6.1. Acid-Base Equilibria

    6.2. Carboxylic Acids and Sulfonic Acids

    6.2.A. Carboxylic Acids

    6.2.B Sulfonic Acids

    6.3. Factors That Influence the Strength of a Carboxylic Acid

    6.3.A. Stability of the Conjugate Base

    6.3.B. Inductive Effects

    6.3.C. Solvent Effects

    6.4. Alcohols Are Amphoteric

    6.5. Amines

    6.6. Carbon Acids

    6.6.A. Terminal Alkynes Are Weak Acids

    6.6.B. -Hydrogen Atoms and Carbonyls

    6.7. Organic Bases

    6.7.A. Amines

    6.7.B. Alcohols Are Bases

    6.7.C. Ethers Are Bases

    6.7.D. Carbonyl Compounds Are Bases

    6.7.E. Alkenes and Alkynes Are Bases

    6.8. Lewis Acids and Bases

    6.9. Nucleophiles

    6.10. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 7. Chemical Reactions, Bond Energy, and Kinetics

    7.1. A Chemical Reaction

    7.2. Reactive Intermediates

    7.2.A. Carbocations (Carbenium ions)

    7.2.B. Carbanions

    7.2.C. Radicals

    7.3 Formal Charge

    7.4. Free Energy: Enthalpy and Entropy

    7.5. Bond Dissociation Enthalpy and Reactions

    7.6. Transition States

    7.7. Competing Reactions

    7.8. Reversible Chemical Reactions

    7.9. Reaction Curves and Intermediates

    7.10. Mechanisms

    7.11. Kinetics

    7.11.A. Reaction Rate and First-Order Reactions

    7.11.B. Second-Order Reactions

    7.11.C. Half Life

    7.11.D. No Reaction

    7.12. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 8: Conformations

    8.1. Rotation Around C-C Bonds

    8.1.A. Staggered and Eclipsed Rotamers

    8.1.B. Torsional Strain: Steric Hindrance and Energy Barriers

    8.2. Longer Chain Alkanes

    8.3. Influence of Heteroatoms on the Rotamer Population

    8.3.A. Halogen Substituents

    8.3.B. OH or NH Groups in Alcohols or Amines

    8.4. Introducing -Bonds

    8.5. Cyclic Alkanes

    8.5.A. Strain and Steric Hindrance in Cyclic Alkanes

    8.5.B. Conformations of C3-C5 Cycloalkanes

    8.5.C. Conformationally Mobile Cyclohexane

    8.6. Substituted Cyclohexanes. A1,3-Strain

    8.7. Large Rings

    8.8 Cyclic Alkenes

    8.9. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 9: Stereoisomers: Chirality, Enantiomers, and Diastereomers

    9.1. Stereogenic Carbons and Stereoisomers

    9.2. Absolute Configuration [(R) and (S) Nomenclature]

    9.3. Specific Rotation: A Physical Property

    9.4. Circular Dichroism

    9.5. Diastereomers

    9.6. Alkenes

    9.7. Cis and Trans Substituents Attached to Rings

    9.8. Stereogenic Centers in Cyclic Molecules

    9.9. Stereogenic Centers in Bicyclic Molecules

    9.10. Optical Resolution

    9.11. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 10: Acid-Base Reactions of -Bonds: Addition Reactions

    10.1. Carbocation Stability

    10.2. Alkenes React With Brønsted-Lowry Acids

    10.3. Carbocation Rearrangements

    10.4. Hydration Reactions of Alkenes

    10.5. Alkenes React With Dihalogens

    10.5.A Dihalogenation

    10.5.B. Diastereoselectivity in the Dihalogenation Reaction of Alkenes

    10.5.C. Reaction With Aqueous Solutions of Halogens (Hypohalous Acids)

    10.6. Alkenes React With Borane

    10.7. Alkenes React With Mercury(II) Compounds

    10.8. Alkynes React as Bases

    10.8.A. Reaction With Brønsted-Lowry Acids

    10.8.B. Hydration of Alkynes

    10.8.C. Dihalogenation of Alkynes

    10.8.D. Hydroboration of Alkynes

    10.8.E. Oxymercuration of Alkynes

    10.9. Metathesis

    10.10. Non-Ionic Reactions: Radical Reactions

    10.11. Polymerization

    10.12. Organization of Reaction Types

    10.13. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 11: Substitution Reactions

    11.1. Alkyl Halides, Sulfonate Esters, and the Electrophilic C-X Bond

    11.2. The SN2 Reaction

    11.2.A. Nucleophilic Approach to an Electrophilic Carbon

    11.2.B. Reaction Rate and Energy Requirements

    11.2.C. The Role of the Solvent

    11.3. Functional Group Transformations Via the SN2 Reaction

    11.4. The SN1 Reaction

    11.5. Substitution Reactions of Alcohols

    11.5.A. Alcohols React With Mineral Acids

    11.5.B. Sulfur and Phosphorous Halide Reagents

    11.5.C. Mitsunobu Reaction

    11.6. Reactions of Ethers

    11.6.A. Ethers React as Brønsted-Lowry Bases

    11.6.B. Reactions of Epoxides

    11.7. Free Radical Halogenation of Alkanes

    11.8. C-H Substitution

    11.9. Organization of Reaction Types

    11.10. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 12: Elimination and p-Bond-Forming Reactions

    12.1. Bimolecular Elimination

    12.2. Stereochemical Consequences of the E2 Reaction

    12.3. The E2 Reaction in Cyclic Molecules

    12.4. Unimolecular Elimination: The E1 Reaction

    12.5. Intramolecular Elimination

    12.6. Elimination Reactions of Vinyl Halides: Formation of Alkynes

    12.7. Substitution versus Elimination

    12.8. Strength and Limitations of the Simplifying Assumptions

    12.9. Organization of Reaction Types

    12.10. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    13: Spectroscopic Methods of Identification

    13.1. Light and Energy

    13.2. Mass Spectrometry

    13.3. Infrared Spectroscopy

    13.3.A. Absorbing Infrared Light and the Infrared Spectrophotometer

    13.3.B. The Infrared Spectrum and Functional Group Absorptions

    13.4. Nuclear Magnetic Resonance Spectroscopy

    13.4.A. The Nuclear Magnetic Resonance Experiment

    13.4.B. The Proton NMR Spectrum

    13.5. Identifying Monofunctional Molecules

    13.6. Carbon-13 NMR Spectroscopy: Counting the Carbons

    13.7. Two-Dimensional (2D)-NMR

    13.8. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 14: Organometallics

    14.1. Organomagnesium Compounds

    14.2. Grignard Reagents Are Bases and Nucleophiles

    14.3. Organolithium Reagents

    14.4. Organocuprates

    14.5. Other Organometallic Compounds

    14.6. Organization of Reaction Types

    14.7. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 15: Oxidation

    15.1. Defining an Oxidation

    15.2. Oxidation of Alcohols

    15.2.A. Chromium (VI) Oxidation of Alcohols

    15.2.B. Swern Oxidation

    15.3. Dihydroxylation of Alkenes

    15.4. Epoxidation of Alkenes

    15.5. Oxidative Cleavage

    15.5. C-H Oxidation

    15.6. Organization of Reaction Types

    15.7. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 16: Reactions of Aldehydes and Ketones

    16.1. Aldehydes and Ketones

    16.2. The Reaction of Ketones and Aldehydes With Strong Nucleophiles

    16.3. Stereoselectivity

    16.4. The Reaction of Ketones and Aldehydes With Weak Nucleophiles

    16.4.A. Reaction With Water

    16.4.B. Reaction With Alcohols

    16.4.C. Reaction With Amines

    16.5. Organization of Reaction Types

    16.6. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 17: Reduction

    17.1 Defining a Reduction

    17.2. Hydride Reducing Agents

    17.3. Hydride Reduction of Other Functional Groups

    17.4. Catalytic Hydrogenation

    17.4.A. Hydrogenation of Alkenes and Alkynes

    17.4.B. Homogeneous Hydrogenation

    17.4.C. Hydrogenation of Heteroatom Functional Groups

    17.5. Dissolving Metal Reductions

    17.6. Organization of Reaction Types

    17.7. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 18: Carboxylic Acid Derivatives and Acyl Substitution

    18.1. Carboxylic Acids

    18.2. Carboxylic Acid Derivatives: Structure and Nomenclature

    18.3. Sulfonic Acids and Derivatives

    18.4. Acyl Substitution and Hydrolysis of Carboxylic Acid Derivatives

    18.5. Preparation of Acid Chlorides and Acid Anhydrides

    18.6. Preparation of Esters

    18.7. Baeyer-Villiger Oxidation

    18.8. Preparation of Amides

    18.9. Carboxylic Acid Derivatives React With Carbon Nucleophiles

    18.10. Dicarboxylic Acid Derivatives

    18.11. Nitrate Esters, Sulfate Esters, and Phosphate Esters

    18.12. Nitriles Are Carboxylic Acid Derivatives

    18.13. Fatty Acids and Lipids

    18.14. Organization of Reaction Types

    18.15. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 19: Aromatic Compounds and Benzene Derivatives

    19.1. Benzene and Aromaticity

    19.2. Functionalized Benzene Derivatives

    19.2.A. Alkyl Substituents (Arenes)

    19.2.B. Functional Groups on the Benzene Ring

    19.3. Electrophilic Aromatic Substitution

    19.3.A. Aromatic Substitution: Halogenation, Nitration, and Sulfonation

    19.3.B. Friedel-Crafts Alkylation

    19.3.C. Friedel-Crafts Acylation

    19.4. Disubstituted Benzene Derivatives

    19.4.A. Regioselectivity

    19.4.B. Activating and Deactivating Substituents

    19.4.C. Halogen Substituents

    19.4.D. Aniline and Aniline Derivatives

    19.5. Polysubstituted Benzene Derivatives

    19.6. Aromatic Coupling Reactions

    19.7. Reduction And Aromatic Compounds

    19.8. Aromaticity in Monocyclic Molecules Other Than Benzene

    19.9. Polynuclear Aromatic Hydrocarbons

    19.9.A. Naphthalene, Anthracene, and Phenanthrene

    19.9.B. Aromatic Substitution Reactions of Polycyclic Hydrocarbons

    19.10. Nucleophilic Aromatic Substitution

    19.11. Aromatic Amines and Diazonium Salts

    19.12. Benzyne Intermediates

    19.13. Synthesis of Aromatic Compounds

    19.14. Spectroscopy of Aromatic Compounds

    19.15. Organization of Reaction Types

    19.16. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 20: Enolate Anions: Acyl Addition and Acyl Substitution

    20.1. Aldehydes and Ketones Are Weak Acids

    20.2. Non-nucleophilic Bases

    20.3. Enolate Alkylation

    20.4. The Aldol Condensation

    20.5. The Zimmerman Model

    20.6. The Intramolecular Aldol Condensation

    20.7. Acid-Catalyzed Aldol Condensations

    20.8. Ester Enolate Anions

    20.8.A. Alkylation of Ester Enolate Anions

    20.8.B. Acyl Substitution and Acyl Addition

    20.8.C. Intramolecular Condensation: The Dieckmann Condensation

    20.8.D. Malonic Ester Enolate Anions

    20.9. Decarboxylation

    20.10. The Knoevenagel Reaction, the Malonic Ester Synthesis,

    and the Acetoacetic Acid Synthesis

    20.11. Yid Reactions

    20.12. Organization of Reaction Types

    20.13. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 21: Difunctional Molecules: Dienes and Conjugated Carbonyl Compounds

    21.1. Conjugation

    21.2. Photochemistry of C=C and C=O

    21.3. Detecting Conjugation With Ultraviolet Spectroscopy

    21.4. Reactions of Conjugated -Bonds

    21.5. Conjugate Addition

    21.6. Reduction of Conjugated Systems

    21.7. Organization of Reaction Types

    21.8. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 22. Difunctional Molecules: Pericyclic Reactions

    22.1. The Diels-Alder Reaction

    22.2. Reactivity of Dienes and Alkenes

    22.3. Selectivity in the Diels-Alder Reaction

    22.4. Other Pericyclic Reactions: [3+2] [2+2]

    22.5. Sigmatropic Rearrangements

    22.6. Organization of Reaction Types

    22.7. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 23: Heteroaromatic Compounds

    23.1. Nitrogen, Oxygen and Sulfur in an Aromatic Ring

    23.2. Substitution Reactions in Monocyclic Heterocyclic Aromatic Compounds

    23.3. Heteroaromatic Compounds With More Than One Ring

    23.4. Aromatic Substitution Reactions of Polycyclic Heterocycles

    23.5. Reduced Heterocycles

    23.6. Alkaloids

    23.7. Biological Relevance

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 24: Multifunctional Compounds:

    Amines, Amino Acids and Peptides

    24.1. Reactions That Form Amines

    24.2. Amino Acids

    24.3. Reactions and Synthesis of -Amino Acids

    24.4. Biological Relevance: Peptides

    24.5. Biological Relevance: Proteins

    24.6. Biological Relevance: Enzymes

    24.7. Combinatorial Methods

    24.8. Amino Acid Residue Identification in Proteins

    24.9. End Group Analysis

    24.10. Hormones

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK

    Chapter 25: Multifunctional Compounds: Carbohydrates

    25.1. Polyhydroxy Carbonyl Compounds

    25.1.A. Monosaccharides

    25.1.B. Hemi-Acetals

    25.1.C. The Anomeric Effect

    25.1.D. Ketose Monosaccharides

    25.1.E. Amino Sugars

    25.2. Disaccharides, Trisaccharides, Oligosaccharides, and Polysaccharides

    25.3. Reactions of Carbohydrates

    25.4. Glycosides

    25.5. Biological Relevance: Nucleosides and Nucleotides

    25.6. Biological Relevance: Polynucleotides

    Correlation of Homework with Concepts

    ANSWERS TO IN-CHAPTER QUESTIONS

    HOMEWORK