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Full Description
To understand and improve the underlying principles that govern how organic reactions occur, A Foundation Course for College Organic Chemistry follows a brick-by-brick building approach. Emphasis is given to interrelating experimental facts and findings with predictions (mechanism) and inferences (results). Discussions focus on clarifying how complex organic reactions occur, which is based on electronegativity differences, movement of electrons (through σ framework or π bonds), and addition or removal of atoms (hydrogen, halogens) or groups (hydroxy, amino).
The book begins with simple rules governing the deconstruction of reactions and applies them to explain how esterification, amide, and cyanide hydrolysis reactions proceed. The importance of stereochemistry (used in drug development, biology, and medicine), aromatic electrophilic and nucleophilic substitutions, reaction kinetics, and dynamics is explained with suitable examples.
Features:
A systematic and structured approach is used to study all aspects of reactive intermediates (generation, structure, geometry, and reactions of carbocations, carbanions, and carbon-free radicals)
This book incorporates scientific methods to deduce reaction mechanisms with simple and relevant explanations, and limitations
A proper explanation is given to understand the influence of functional groups on the stability and reactivity of intermediates, pKa, HSAB principles, structure-activity relations, and how these can be exploited in organic chemistry
Information is presented in an accessible way for students, teachers, researchers, and scientists
Contents
1 Deconstruction of organic reactions
2 Geometric isomerism
3 Conformational isomerism: open chain and cyclic systems
4 Basics of Symmetry elements and point groups
5 Stereochemical conventions and topicity
6 Chiroptical properties
7 Stereochemical reactions
8 Aromaticity and polyaromatic compounds
9 Aromatic electrophilic and nucleophilic substitutions
10 Reaction dynamics and reaction kinetics
11 Reactive intermediates: carbocations
12 Reactive intermediates: carbanions
13 Reactive intermediates: Free radicals
14 Reactive intermediates: Carbenes and nitrenes
15 Carbon-carbon bond formation using carbon nucleophiles: enolates, enamines and enol ethers
16 Name reactions
