Reactive Intermediates in Organic Chemistry Structure Mechanism and Reactions 1st Edition by Singh Maya Shankar ISBN 978-3527678266 3527678266
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Product details:
ISBN 10: 3527678266
ISBN 13: 978-3527678266
Author: Singh Maya Shankar
Most reactions in organic chemistry do not proceed in a single step but rather take several steps to yield the desired product. In the course of these multi-step reaction sequences, short-lived intermediates can be generated that quickly convert into other intermediates, reactants, products or side products. As these intermediates are highly reactive, they cannot usually be isolated, but their existence and structure can be proved by theoretical and experimental methods. Using the information obtained, researchers can better understand the underlying reaction mechanism of a certain organic transformation and thus develop novel strategies for efficient organic synthesis.
The chapters are clearly structured and are arranged according to the type of intermediate, providing information on the formation, characterization, stereochemistry, stability, and reactivity of the intermediates. Additionally, representative examples and a problem section with different levels of difficulty are included for self-testing the newly acquired knowledge.
By providing a deeper understanding of the underlying concepts, this is a musthave reference for PhD and Master Students in organic chemistry, as well as a valuable source of information for chemists in academia and industry working in the field. It is also ideal as primary or supplementary reading for courses on organic chemistry, physical organic chemistry or analytical chemistry.
Table of contents:
-
Introduction
1.1 Reaction Mechanism and Reaction Arrows
1.2 Properties and Characteristics of a Reaction
1.3 Summary -
Carbocations
2.1 Introduction
2.2 History
2.3 Sturctures and Geometry of Carbocations
2.4 Generation of Carbocation
2.5 Carbocation Stability
2.6 Detection of Carbocations
2.7 Fate of Carbocations
2.8 Nonclassical Carbocations
2.9 Radical Cations
2.10 Summary -
Carbanions
3.1 Structure and Geometry of Carbanions
3.2 Generation of Carbanions
3.3 Stability of Carbanions
3.4 Reactions of Carbanions
3.5 Enolate Reactions with Carbonyl Groups
3.6 Rearrangements of Carbanions
3.7 Chiral Carbanions
3.8 Carbanions and Tautomerism
3.9 Summary -
Radicals
4.1 Introduction
4.2 Detection and Characterization of Radicals
4.3 Structure and Bonding of Radicals
4.4 Generation of Free Radicals
4.5 Stability of Radicals
4.6 Reactions of Free Radicals
4.7 Stereochemistry of Radical Reactions
4.8 Biradicals
4.9 Summary -
Carbenes
5.1 Structure and Geometry of Carbenes
5.2 Generation of Carbenes
5.3 Reactions of Carbenes
5.4 Carbenes and Carbene Ligands in Organometallic Chemistry
5.5 Summary -
Nitrenes
6.1 Introduction
6.2 Structure and Reactivity
6.3 Generation of Nitrenes
6.4 Reactions of Nitrenes
6.5 Summary -
Miscellaneous Intermediates
7.1 Arynes
7.2 Ketenes and Cumulenes
7.3 ortho-Quinone Methides
7.4 Zwitterions and Dipoles
7.5 Antiaromatic Systems
7.6 Tetrahedral Intermediates
7.7 Summary
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Tags: Singh Maya Shankar, Reactive Intermediates, Organic Chemistry, Mechanism and Reactions