A01=Michael Edenborough
acid
acid/base characteristics
acidbase characteristics
advanced organic mechanism strategies
Aromatic Sextet
atoms
Author_Michael Edenborough
base characteristics
bond
Cahn Ingold Prelog Rules
carbon
Carbon Double Bond
carbonium
Carbonium Ion
Carbonyl Carbon
Carbonyl Compound
Category=PNN
Category=PNR
Cyclic Transition State
Cyclic Version
double
electron counting
Electrophilic Substitution
elimination
Elimination Reaction
Enol Tautomer
eq_bestseller
eq_isMigrated=1
eq_isMigrated=2
eq_nobargain
eq_non-fiction
eq_science
Hydrogen Cation
Hydroxide Anion
incoming
Incoming Nucleophile
kinetic isotope effect
Leaving Group
lone
Lone Pairs
mechanistic pathways
Meerwein Ponndorf Verley Reduction
Mesomeric Effect
Methoxide Anion
molecular orbital analysis
nucleophile
Organic Reaction Mechanisms
Oxygen Double Bond
pair
physical organic chemistry
redox reaction
Single Covalent Bond
Substitution Reactions
transition state theory
undergraduate chemistry course
Valence Shell
Vice Versa
Product details
- ISBN 9781138455979
- Weight: 453g
- Dimensions: 156 x 234mm
- Publication Date: 11 Aug 2017
- Publisher: Taylor & Francis Ltd
- Publication City/Country: GB
- Product Form: Hardback
Secure
checkout
Fast Shipping
Easy returns
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.
