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writing-reactionWriting Reaction Mechanisms in Organic Chemistry, Second Edition, is an invaluable guide to charting the movements of atoms and electrons in the reactions of organic molecules. Miller and Solomon illustrate that understanding organic reactions is based on applying general principles rather than the rote memorization of unrelated processes, and, in turn, emphasize that writing mechanisms is a practical method of applying knowledge of previously encountered reactions and reaction conditions to new reactions. Students and research chemists alike will find this book useful in providing a method of organizing and synthesizing an oftentimes overwhelming quantity of information into a set of general principles and guidelines for determining and describing organic reaction mechanisms.

NEW TO THIS EDITION
( Illustrated with hundreds of chemical structures, all redrawn from the first edition, with added
emphasis on three-dimensional structures and stereochemical aspects of reaction mechanisms
( Extensively rewritten and reorganized to make the presentation and format more accessible to first-year organic chemistry students, as well as advanced undergraduate and graduate students
( Chapter 6 is completely revised to streamline the treatment of pericyclic reactions, while introducing the principles underlying the symmetry operations and orbital correlation diagrams
( New appendixes in this edition contain easily referenced information on Lewis structures, chemical symbols and notation, and relative acidities of common functional groups

Table of Contents

  • Preface to the Second Edition, Preface to the First Edition
  • Chapter 1 – Introduction—Molecular Structure and Reactivity, Pages 1-62
  • Chapter 2 – General Principles for Writing Reaction Mechanisms, Pages 63-103
  • Chapter 3 – Reactions of Nucleophiles and Bases, Pages 105-193
  • Chapter 4 – Reactions Involving Acids and Other Electrophiles, Pages 195-281
  • Chapter 5 – Radicals and Radical Anions, Pages 283-342
  • Chapter 6 – Pericyclic Reactions, Pages 343-416
  • Chapter 7 – Additional Problems, Pages 417-451
  • Appendix A – Lewis Structures of Common Functional Groups, Pages 453-454
  • Appendix B – Symbols and Abbreviations Used in Chemical Notation, Pages 455-456
  • Appendix C – Relative Acidities of Common Organic and Inorganic Substances, Pages 457-464
  • Index, Pages 465-471

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