Organic Chemistry / Edition 4

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Overview

This package includes G. Marc Loudon's textbook Organic Chemistry, Fourth Edition (0-19-511999-1) and its accompanying Study Guide/Solutions Manual (0-19-512000-0) at a discounted price.

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Product Details

  • ISBN-13: 9780195159127
  • Publisher: Oxford University Press, USA
  • Publication date: 5/28/2003
  • Series: Organic Chemistry Ser.
  • Edition description: REV
  • Edition number: 4
  • Product dimensions: 10.90 (w) x 8.90 (h) x 3.40 (d)

Meet the Author

Purdue University
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Table of Contents

1 What is organic chemistry? 1
Organic chemistry and this book 13
2 Organic structures 19
3 Determining organic structures 47
4 Structure of molecules 81
5 Organic reactions 113
6 Nucleophilic addition to the carbonyl group 135
7 Delocalization and conjugation 151
8 Acidity, basicity, and pK[subscript a] 181
9 Using organometallic reagents to make C-C bonds 209
10 Conjugate addition 227
11 Proton nuclear magnetic resonance 243
12 Nucleophilic substitution at the carbonyl (C=O) group 279
13 Equilibria, rates, and mechanisms: summary of mechanistic principles 305
14 Nucleophilic substitution at C=O with loss of carbonyl oxygen 339
15 Review of spectroscopic methods 361
16 Stereochemistry 381
17 Nucleophilic substitution at saturated carbon 407
18 Conformational analysis 447
19 Elimination reactions 477
20 Electrophilic addition to alkenes 503
21 Formation and reactions of enols and enolates 523
22 Electrophilic aromatic substitution 547
23 Electrophilic alkenes 581
24 Chemoselectivity: selective reactions and protection 615
25 Synthesis in action 643
26 Alkylation of enolates 663
27 Reactions of enolates with aldehydes and ketones: the aldol reaction 689
28 Acylation at carbon 723
29 Conjugate addition of enolates 749
30 Retrosynthetic analysis 771
31 Controlling the geometry of double bonds 803
32 Determination of stereochemistry by spectroscopic methods 823
33 Stereoselective reactions of cyclic compounds 851
34 Diastereoselectivity 881
35 Pericyclic reactions 1: cycloadditions 905
36 Pericyclic reactions 2: sigmatropic and electrocyclic reactions 943
37 Rearrangements 969
38 Fragmentation 1003
39 Radical reactions 1021
40 Synthesis and reactions of carbenes 1053
41 Determining reaction mechanisms 1079
42 Saturated heterocycles and stereoelectronics 1121
43 Aromatic heterocycles 1: structures and reactions 1147
44 Aromatic heterocycles 2: synthesis 1185
45 Asymmetric synthesis 1219
46 Organo-main-group chemistry 1: sulfur 1247
47 Organo-main-group chemistry 2: boron, silicon, and tin 1277
48 Organometallic chemistry 1311
49 The chemistry of life 1345
50 Mechanisms in biological chemistry 1381
51 Natural products 1413
52 Polymerization 1451
53 Organic chemistry today 1481
Index 1491
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Sort by: Showing all of 2 Customer Reviews
  • Anonymous

    Posted November 21, 2009

    I Also Recommend:

    Excellent Classic Organic Text

    Great book that professors can adapt for classes for students aspiring to grad school, or for a more basic class. I used this as an undergrad before deciding to get my PhD. I tutored for many years and have seen professors at various colleges adapt the text to the level they want to teach at. Great descriptive, real life applications throughout the book as expanded assides.

    Was this review helpful? Yes  No   Report this review
  • Anonymous

    Posted January 9, 2003

    A Waste

    This book was a great dissapointment. The main problem being that it packs way too much information in with out doing a good job of explaining or simplifying the material, which by the way should be the main aim of any text book. Organic Chemistry is usually a dull and difficult subject and this book does a good job of improving this negative reputation. The book seems to have been written for a professor or a graduate student as opposed to a student taking the course for the first time. My advice is to study from another book or convince your professor to change to another text.

    0 out of 1 people found this review helpful.

    Was this review helpful? Yes  No   Report this review
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