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Advances in Physical Organic Chemistry
 
 

Advances in Physical Organic Chemistry, 1st Edition

 
Advances in Physical Organic Chemistry, 1st Edition,John Richard,Thomas Tidwell,ISBN9780120335374
 
 
 

Advances in Physical Organic Chemistry

Richard   &   Tidwell   

Academic Press

9780120335374

373

The latest volume in the highly successful Advances in Physical Organic Chemistry series

Print Book

Hardcover

In Stock

Estimated Delivery Time
USD 270.00
 
 

Key Features

. Volume 37 of this hugely successful Advances in Physical Organic Chemistry series
. Comprehensive review articles covering various topics of interest within the physical organic chemistry field

Description

Advances in Physical Organic Chemistry provides the chemical community with authoritative and critical assessments of the many aspects of physical organic chemistry. The field is a fast developing one, with results and methodologies finding application from biology to solid state physics.

This latest volume deals comprehensively with investigations that can be traced back to the birth of the field but which are still proving critical to the understanding of the stability of organic molecules and the mechanisms for their reactions.

Readership

For organic and physical chemists and biochemists.

John Richard

Affiliations and Expertise

Department of Chemistry, University of Buffalo, NY, U.S.A.

View additional works by John P. Richard

Thomas Tidwell

Affiliations and Expertise

University of Toronto, Ontario, Canada

Advances in Physical Organic Chemistry, 1st Edition

Introduction.

Quantitative thermodynamic criteria of stability in the gas phase. Definitions and experimental techniques. The specific case of carbocations.

Theoretical calculations.

Uncertainties.

Thermodynamics and structure of selected species. Carbocations C1 to C4. Aliphatic carbocations with more than five carbon atoms. Cyclic species without formal systems. Cyclopropyl-substituted carbonations. Secondary and tertiary carbocations derived from cage hydrocarbons. Carbenium ions with formal systems. Two-electron aromatic and homoaromatic ions. Six-electron aromatic ions. Phenyl-substituted carbocations.

Solution reactivity. Thermodynamic properties. Reaction kinetics.

 
 
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