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Organic Reaction Mechanisms: A Step by Step Approach, Second Edition
 
 
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Organic Reaction Mechanisms: A Step by Step Approach, Second Edition [Paperback]

Michael Edenborough (Author)

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Book Description

0748406417 978-0748406418 November 27, 1998 2
This text is designed to teach students how to write organic reaction mechanisms. It starts from the absolute basics - counting the numbers of electrons around a simple atom. Then, in small steps, the text progresses to advanced mechanisms. the end, all the major mechanistic routes have been covered. The text is in the form of interactive sections, which are designed to facilitate the assimilation of the information conveyed, so that by the end the student should already know the contents without the need for extensive revision.

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Inside This Book (learn more)
First Sentence:
The ability to count correctly the number of electrons around any given atom is central to being able to write a plausible reaction mechanism in organic chemistry. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
mesomeric groups, resultant carbonium ion, tetrahedral mechanism, vinyl carbonium ion, crotonaldehyde reaction, homoatomic bond, catalysed ester hydrolysis, principal quantum level, principal quantum shell, heteroatomic bonds, migration terminus, resultant alkene, same oxidation number, secondary carbonium ion, radical substitution reactions, permanent charge separation, attacking species, primary carbonium ion, resultant anion, incoming electrophile, orbital projects, ethoxide anion, bromine molecule, leaving group departs, cyclic bromonium ion
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Periodic Table, Norrish Type
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