stereochemistry of macromolecules
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stereochemistry of macromolecules

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Published by Edward Arnold in London .
Written in English

Book details:

Edition Notes

Originally published, New York: Dekker, 1968.

Statementedited by A.D. Ketley. Vol.3.
ContributionsKetley, A. D.
The Physical Object
Pagination460p. :
Number of Pages460
ID Numbers
Open LibraryOL18315595M
ISBN 100713160667

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The Stereochemistry of Linear Macromolecules. Mario Farina. Dipartimento di Chimica Organica e Industriale, Università di Milano, Milano, Italy Università di Milano, Milano, Italy. Search for more papers by this author. Book Editor(s): Ernest L. Eliel. University of North Carolina, Chapel Hill, North Carolina The Contribution of NMR Cited by: This article was written to provide an introduction to the basic concepts of polymer stereochemistry and their applications. Stereochemistry and macromolecules: Principles and applications | Journal of Chemical EducationCited by: 3. Although stereochemistry plays a key role in the structure and function of biological polymers it was not until the discovery of isotactic polypropylene, now about 60 years ago, that the role of Author: Mario Farina. Stereochemistry is defined as the study of the three-dimensional structure of molecules. Stereochemical considerations are important in both isomerism and studies of the mechanisms of chemical reactions. Implicit in a mechanism is the stereochemistry of the reaction: in other words, the relative three-dimensional orientation 4/5(2).

About this book This seminal series, first edited by Ernest Eliel, responsible for some of the major advances in stereochemistry and the winner of the ACS Priestley Medal in , provides coverage of the major developments of the field of stereochemistry. Stereochemistry an introduction (PDF 40P) This note covers the following topics: Stereochemistry of Tetrahedral Carbons, Stereoisomers Stereoisomers, Stereocenter, Chiral, Enantiomers, Racemic mixture, Configuration of Stereocenters, Molecules with multiple stereocenters, Tartaric Acid and Enantiomers. Author(s): Grazia Piizzi, Steve Hardinger. The importance of stereochemistry in drug action is gaining greater attention in medical practice, and a basic knowledge of the subject will be necessary for clinicians to make informed decisions regarding the use of single-enantiomer drugs. Many of the drugs currently Cited by: The Stereochemistry of Linear Macromolecules. ,,, DOI: /ch1. Irene Sessa, Zsolt Csok, Adolfo Zambelli. Molecular Structure of C-C2H4/C3H6 Copolymers Prepared in the Presence of Half Sandwich Titanium Methyl - B(C6F5)3 by:

Ch05 Stereochemistry (landscape).doc Page 3 Common Chiral Objects Chirality in Organic Molecules If a mirror image of a molecule can be placed on top of the original, and the 3 dimensional arrangement of every atom is the same, then the two molecules are superimposable, and the molecule is achiral. If a molecule has a non superimposable mirror image, it is Size: 1MB. Additional Physical Format: Online version: Ketley, A.D. Stereochemistry of macromolecules. New York, M. Dekker, (OCoLC) Document Type. CHAPTER 6: STEREOCHEMISTRY. Projecting away from the viewer Projecting toward the viewer Hydrogens projecting toward the viewer The convention used in this book. it moves further away. Yet, this is the most common convention used, and it is the con- vention we adopt in this book. Basic Stereochemistry of Organic Molecules. Subrata Sengupta. About the Book To find out more and read a sample chapter see the catalogue. Student Resources. The online resources for Students include wide range of textbook-linked resources for 'll need your Oxford ID login details to access these free resources. If you are not.