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Editorial Reviews
Review
`The subject is presented authoritatively, systematically and concisely without resort to mathematical treatment. As this subject is often given little coverage in textbooks or organic chemistry this text is to be welcomed.' Aslib Book Guide, vol.61, no.11, November 1996
`This book is a useful introduction to stereo-electronic effects in organic chemistry. The style is engaging ... this book is an excellent supplementary text for undergraduates. Sponsorship for the series by Zeneca also ensures that it is extremely good value for money.' Chemistry in Britain, September 1997
`engaging critique of biography .... enjoyable and thought provoking' New Scientist
Product Description
Stereoelectronic effects control the way molecules are put together and account for the "rules of engagement" which operate when molecules meet and react. Understanding these effects is the key to understanding molecular behavior, since the same basic three-dimensional interactions are responsible for both structure and reactivity. This concise and very accessible volume provides a comprehensive, intentionally non-mathematical coverage of stereochemistry, along with an in-depth discussion of the main classes of organic reactions, promoting a logical and simple way of thinking about chemistry.
See all Editorial Reviews
`The subject is presented authoritatively, systematically and concisely without resort to mathematical treatment. As this subject is often given little coverage in textbooks or organic chemistry this text is to be welcomed.' Aslib Book Guide, vol.61, no.11, November 1996
`This book is a useful introduction to stereo-electronic effects in organic chemistry. The style is engaging ... this book is an excellent supplementary text for undergraduates. Sponsorship for the series by Zeneca also ensures that it is extremely good value for money.' Chemistry in Britain, September 1997
`engaging critique of biography .... enjoyable and thought provoking' New Scientist
Product Description
Stereoelectronic effects control the way molecules are put together and account for the "rules of engagement" which operate when molecules meet and react. Understanding these effects is the key to understanding molecular behavior, since the same basic three-dimensional interactions are responsible for both structure and reactivity. This concise and very accessible volume provides a comprehensive, intentionally non-mathematical coverage of stereochemistry, along with an in-depth discussion of the main classes of organic reactions, promoting a logical and simple way of thinking about chemistry.
See all Editorial Reviews
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Inside This Book
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First Sentence:
A molecule's bonding electrons serve not only as its skeleton, but also as a rudimentary nervous system. Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
developing carbocation, stereoelectronic effects, efficient overlap, axial isomer, anomeric effect, electronic strain, negative hyperconjugation, steric preference, interacting orbitals, equatorial isomer, stereoelectronic control, electronic basis, carbon centre, incoming nucleophile, preferred geometry, orbital interactions, electrophilic attack, vacant orbitals, angle strain, lone pair, ionic reactions, antibonding orbital, gauche conformation, intramolecular reactions, leaving group Key Phrases - Capitalized Phrases (CAPs): (learn more)
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Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
A molecule's bonding electrons serve not only as its skeleton, but also as a rudimentary nervous system. Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
developing carbocation, stereoelectronic effects, efficient overlap, axial isomer, anomeric effect, electronic strain, negative hyperconjugation, steric preference, interacting orbitals, equatorial isomer, stereoelectronic control, electronic basis, carbon centre, incoming nucleophile, preferred geometry, orbital interactions, electrophilic attack, vacant orbitals, angle strain, lone pair, ionic reactions, antibonding orbital, gauche conformation, intramolecular reactions, leaving group Key Phrases - Capitalized Phrases (CAPs): (learn more)
New York, Hammond Postulate New!
Books on Related Topics | Concordance | Text Stats Browse Sample Pages:
Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
Citations (learn more)
This book cites 9
books:
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31
books
cite this book:
See all 31 books citing this book
- Mechanism and Theory in Organic Chemistry (3rd Edition) by Thomas H. Lowry on page 48, page 75, and page 88
- Organic Chemistry by Wiley on page 33
- Reactive Intermediates (Oxford Chemistry Primers, No 8) by Christopher J. Moody on page 88
- The Anomeric Effect (New Directions in Organic and Biological Chemistry) by Eusebio Juaristi on page 22
- Frontier Orbitals and Organic Chemical Reactions by Ian Fleming on page 12
See all 9 books this book cites
- The Anomeric Effect (New Directions in Organic and Biological Chemistry) by Eusebio Juaristi on 11 pages
- Advances in Carbohydrate Chemistry and Biochemistry, Vol. 56 by Derek Horton on page 59, page 60, and Back Matter
- Applications of Mass Spectrometry to Organic Sterochemistry (Methods in Stereochemical Analysis) by J. S. Splitter on page 14, page 294, and page 480
- Organic Stereochemistry (Oxford Chemistry Primers) by Michael J. T. Robinson in Front Matter, and page 36
- Introduction to Stereochemistry and Conformational Analysis by Eusebio Juaristi on page 89, and page 298
See all 31 books citing this book
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