Publisher description for Basic organic stereochemistry / Ernest L. Eliel, Samuel H. Wilen, Michael P. Doyle.

Bibliographic record and links to related information available from the Library of Congress catalog

Information from electronic data provided by the publisher. May be incomplete or contain other coding.

Counter Stereoisomers are compounds with the same chemical formula and connectivity but with different arrangements of their atoms in 3-dimensional space. Stereochemistry encompasses the study of stereoisomers and their properties. Despite having an identical chemical formula, stereoisomers can have drastically different biological, medicinal, and chemical properties. Basic Organic Stereochemistry explains in clear, concise terms the concepts and properties of stereoisomers. Ideal both as a text for advanced undergraduate or graduate students and as a handy guide for researchers in industry, this superb text covers: Polarimetry and optical rotation Internal coordinates, configuration, and conformation Nature of stereoisomers Barriers between stereoisomers and residual stereoisomers Symmetry operators and symmetry point groups Properties of stereoisomers and stereoisomer discrimination Separation of stereoisomers, resolution, and racemization Suitable for students in organic and biological chemistry, Basic Organic Stereochemistry is unparalleled as a convenient text.

Library of Congress subject headings for this publication: Stereochemistry