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Produktbild: How to Succeed in Organic Chemistry

How to Succeed in Organic Chemistry

118,99 €

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Beschreibung

Produktdetails

Einband

Taschenbuch

Erscheinungsdatum

20.03.2020

Verlag

Oxford University Press

Seitenzahl

520

Maße (L/B/H)

24,4/17/2,8 cm

Gewicht

900 g

Sprache

Englisch

ISBN

978-0-19-885129-5

Beschreibung

Produktdetails

Einband

Taschenbuch

Erscheinungsdatum

20.03.2020

Verlag

Oxford University Press

Seitenzahl

520

Maße (L/B/H)

24,4/17/2,8 cm

Gewicht

900 g

Sprache

Englisch

ISBN

978-0-19-885129-5

Herstelleradresse

Libri GmbH
Europaallee 1
36244 Bad Hersfeld
DE

Email: gpsr@libri.de

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  • Produktbild: How to Succeed in Organic Chemistry

    • Section 1: Laying the Foundations

    • Basics 1: Structures of Organic Compounds

    • Habit 1: Always Draw Structures with Realistic Geometry

    • Basics 2: Functional Groups and "R" Groups

    • Basics 3: Naming Organic Compounds

    • Practice 1: Drawing Structures from Chemical Names

    • Basics 4: Isomerism in Organic Chemistry - Constitutional Isomers

    • Practice 2: Constitutional Isomers and Chemical Names

    • Habit 2: Identifying When a Formula is Possible

    • Practice 3: Double Bond Equivalents

    • Common Error 1: Formulae, Functional Groups and Double Bond Equivalents

    • Habit 3: Ignore What Doesn't Change

    • Basics 5: Electronegativity, Bond Polarisation and Inductive Effects

    • Practice 4: Bond Polarisation and Electronegativity

    • Basics 6: Bonding in Organic Compounds

    • Practice 5: Hybridisation

    • Basics 7: Bonding and Antibonding Orbitals

    • Basics 8: Introduction to Curly Arrows

    • Fundamental Reaction Type 1: Nucleophilic Substitution at Saturated Carbon

    • Practice 6: Electronegativity in Context

    • Fundamental Reaction Type 2: Elimination Reactions

    • Section 2: Building on the Foundations

    • Basics 9: Breaking Bonds - Linking Curly Arrows and Molecular Orbitals

    • Common Error 2: Curly Arrows

    • Basics 10: Conjugation and Resonance

    • Basics 11: Thermodynamic Definitions

    • Basics 12: Bond Dissociation Energy

    • Basics 13: Calculating Enthalpy of Reaction from Bond Dissociation Energies

    • Perspective 1: A Closer Look at Bond Dissociation Energies

    • Practice 7: Calculating Enthalpy of Reaction from Bond Dissociation Energy

    • Basics 14: Energetics and Reaction Profiles

    • Basics 15: How Fast Are Reactions?

    • Basics 16: Introduction to Carbocations, Carbanions and Free-Radicals

    • Basics 17: Carbocations 2 - More Factors Affecting Stability

    • Basics 18: Carbanions 2 - Stability and pKa

    • Perspective 2: A Scale for Carbocation Stability

    • Common Error 3: Methyl Groups are Electron-Releasing

    • Practice 8: Drawing Resonance Forms for Carbocations and Carbanions

    • Common Error 4: Resonance

    • Basics 19: The Hammond Postulate

    • Basics 20: Conjugation and Stability - The Evidence

    • Common Error 5: Carbocations and Carbanions

    • Basics 21: Reactivity of Conjugated Systems

    • Basics 22: Acid Catalysis in Organic Reactions Part 1

    • Reaction Detail 1: Nucleophilic Substitution at Saturated Carbon

    • Basics 23: What Defines a Transition State?

    • Perspective 3: Bonding Beyond Hybridisation

    • Fundamental Knowledge Recap 1: Bond Lengths and Strengths

    • Fundamental Knowledge Recap 2: pKa

    • Section 3: A Focus on Shape

    • Habit 4: Representing Stereochemistry - Flying Wedge and Newman Projections

    • Basics 23: Isomerism in Organic Chemistry - Configurational Isomers

    • Habit 5: Getting Used to Drawing Stereoisomers

    • Practice 9: Getting Used to Stereoisomers

    • Habit 6: Assignment of Stereochemistry - The Cahn-Ingold-Prelog Rules

    • Practice 10: Assigning Stereochemistry

    • Habit 7: Stereoisomers with Symmetry

    • Basics 25: Properties of Stereoisomers

    • Reaction Detail 2: Stereochemical Aspects of Substitution Reactions

    • Common Error 6: Substitution Reactions

    • Reaction Detail 3: Substitution with Retention of Configuration

    • Common Error 7: Stereochemical Errors

    • Section 4: Types of Selectivity

    • Basics 26: Selectivity in Organic Chemistry - Chemoselectivity

    • Basics 27: Selectivity in Organic Chemistry - Regioselectivity

    • Basics 28: Selectivity in Organic Chemistry - Stereoselectivity

    • Basics 29: Stereochemical Definitions Relating to Reactions

    • Section 5: Bonds Can Rotate

    • Basics 30: Isomerism in Organic Chemistry - Conformational Isomers

    • Practice 11: Conformational Analysis

    • Applications 1: Conformational Isomers 2

    • Applications 2: SN2 Substitution Reactions Forming Three-Membered Rings

    • Basics 31: Introduction to Cyclohexanes

    • Practice 12: Drawing Cyclohexanes

    • Applications 3: Substitution Reactions of Cyclohexanes

    • Basics 32: Quantifying Conformers of Cyclohexanes

    • Basics 33: More Conformers of Cyclohexanes and Related Compounds

    • Practice 13: Drawing More Complex Cyclohexanes

    • Common Error 8: Cyclohexanes

    • Section 6: Eliminating the Learning

    • Reaction Detail 4: Elimination Reactions

    • Perspective 4: A Continuum of Mechanisms

    • Basics 34: More Substituted Alkenes Are More Stable

    • Basics 35: Enthalpy Changes for Reactions Involving Anionic Species

    • Applications 4: Stereochemistry of Elimination Reactions

    • Basics 36: Stereospecificity

    • Applications 5: Elimination Reactions of Cyclohexanes

    • Common Error 9: Elimination Reaction

    • Reaction Detail 5: Allylic Substitution

    • Section 7: Building Skills

    • Worked Problem 1: Curly Arrows and Reaction Profiles

    • Worked Problem 2: Competing SN1 Substitution and E1 Elimination

    • Worked Problem 3: Competing SN2 Substitution and E2 Elimination

    • Worked Problem 4: Acid Catalysis in Organic Reactions Part 2

    • Worked Problem 5: Epoxide Opening Reactions

    • Worked Problem 6: Is cis-Cyclohexane-1,2-diol Really Achiral?

    • Worked Problem 7: The Furst-Plattner Rule

    • Worked Problem 8: SN2' Stereochemistry and Conformations

    • Worked Problem 9: Complex Substitution Stereochemistry

    • Worked Problem 10: Cyclisation Reactions

    • Solution to Problem 1: Curly Arrows and Reaction Profiles

    • Solution to Problem 2: Competing SN1 Substitution and E1 Elimination

    • Solution to Problem 3: Competing SN2 Substitution and E2 Elimination

    • Solution to Problem 4: Acid Catalysis in Organic Reactions Part 2

    • Solution to Problem 5: Epoxide Opening Reactions

    • Solution to Problem 6: Is cis-Cyclohexane-1,2-diol Really Achiral?

    • Solution to Problem 7: The Furst-Plattner Rule

    • Solution to Problem 8: SN2' Stereochemistry and Conformations

    • Solution to Problem 9: Complex Substitution Stereochemistry

    • Solution to Problem 10: Cyclisation Reactions