Retentive Solvolysis. 16. Reinvestigation of the Retentive Phenolysis of 1-Phenylethyl Chloride. The Mechanism and the Structure of Ion Pair Intermediate-Reference-Cited by-同舟云学术

Retentive Solvolysis. 16. Reinvestigation of the Retentive Phenolysis of 1-Phenylethyl Chloride. The Mechanism and the Structure of Ion Pair Intermediate

Published:1988-09 Issue:9 Volume:61 Page:3273-3282
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Kinoshita Tomomi,Ueno Takuya,Ikai Keizo,Fujiwara Masataka,Okamoto Kunio

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/61/9/61_9_3273/_pdf

Reference49 articles.

1. Retentive Solvolysis. 15. Salt Effect on the Retentive Phenolyses of 1-(p-Substituted phenyl)ethylp-Nitrobenzoates. The Pattern of Salt Effect and the Number of Ion-Pair Intermediates in the SN1 Solvolysis

2. Kinetic Studies of Solvolysis. XI. The Steric Course of the Phenolyses of Optically Active α-Phenylethyl Chloride in Mixtures of Various Phenols and Organic Solvents—A Mechanism for the SN1 Reaction with a Net Retention of Configuration

3. The Retentive Solvolysis. VII. Structural Effect of the Leaving Group on the Steric Course of the SN1 Phenolysis of 1-Phenylethyl Systems

4. Salt Effects and Ion Pairs in Solvolysis and Related Reactions. IX. The threo-3-p-Anisyl-2-butyl System1-3

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