Solvation effects in the heterolyses of 3‐X‐3‐methylpentanes (X = Cl, Br, I)-Reference-Cited by-同舟云学术

Solvation effects in the heterolyses of 3‐X‐3‐methylpentanes (X = Cl, Br, I)

Published:2004-07-27 Issue:11 Volume:17 Page:1061-1066
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Martins Filomena¹,Leitão Ruben Elvas²,Moreira Luís¹

Affiliation:

1. Department of Chemistry and Biochemistry, Faculty of Sciences, University of Lisbon, CQB, Ed. C8, Campo Grande 1749‐016 Lisbon, Portugal

2. Department of Chemical Engineering, Engineering Institute (ISEL), Polytechnic Institute of Lisbon, CQB, R. Conselheiro Emídio Navarro, 1900 Lisbon, Portugal

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/poc.816

Reference39 articles.

1. Linear solvation energy relationships. Part 37. An analysis of contributions of dipolarity–polarisability, nucleophilic assistance, electrophilic assistance, and cavity terms to solvent effects on t-butyl halide solvolysis rates

2. The SN2-SN1 spectrum. 4. The SN2 (intermediate) mechanism for solvolyses of tert-butyl chloride: a revised Y scale of solvent ionizing power based on solvolyses of 1-adamantyl chloride

3. Is the tert-Butyl Chloride Solvolysis the Most Misunderstood Reaction in Organic Chemistry? Evidence Against Nucleophilic Solvent Participation in the tert-Butyl Chloride Transition State and for Increased Hydrogen Bond Donation to the 1-Adamantyl Chloride Solvolysis Transition State

4. The Correlation of Solvolysis Rates

5. The Correlation of Solvolysis Rates and the Classification of Solvolysis Reactions into Mechanistic Categories

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