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Number 88 in the well-known Oxford Chemistry Primer series introduces upper-undergraduate students to how the three-dimensional shapes of molecules influence their chemical and physical properties. It starts with an introduction to common stereochemical terms used throughout the book. Chapter two covers the structures of simple unstrained organic molecules followed by examples of strained molecules. The third chapter deals with conformational analysis of acyclic and carbocyclic molecules, ending with a short exposition of molecular mechanics. Chapter four is about stereoisomerism in molecules and compounds. A full description of enantiomerism and diastereomerism is followed by an explanation of the nomenclature for absolute and relative configurations of molecules and for topism. The book concludes with a survey of stereoselective and stereospecific reactions, including the use of chiral catalysts and auxiliaries, rules for predicting stereoselectivity, and double asymmetric synthesis.
This text investigates how the three-dimensional spatial arrangement of atoms within organic molecules dictates their physical and chemical behavior. Author Michael J. T. Robinson, drawing on his expertise in chemical education, provides a structured framework for understanding stereochemical principles. The book synthesizes foundational terminology with advanced concepts in molecular mechanics and reaction selectivity to prepare students for complex chemical analysis.
What You Will Find
Experts identify this volume as a standard instructional resource for upper-undergraduate chemistry students. Readers frequently note the technical density of the prose, which requires a solid grasp of foundational organic chemistry to fully comprehend the presented mechanisms.
Page Count:
96
Publication Date:
2001-05-10
Publisher:
Oxford University Press
ISBN-10:
0198792751
ISBN-13:
9780198792758
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