The following is a nucleophilic substitution reaction of S-3-chloro-2-methylhexane with "CN. The experimental rate law for this reaction is Rate = k [S-3-chloro-2-methylhexane] CH3 H,C. H CH, + CEN H2 The mechanism for this reaction is Sy1

The following is a nucleophilic substitution reaction of S-3-chloro-2-methylhexane with "CN. The experimental rate law for this reaction is Rate = k [S-3-chloro-2-methylhexane] CH3 H,C. H CH, + CEN H2 The mechanism for this reaction is Sy1

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter20: Dienes, Conjugated Systems, And Pericyclic Reactions

Section: Chapter Questions

Problem 20.27P

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Question

The following is a nucleophilic substitution reaction of S-3-chloro-2-methylhexane with "CN.
The experimental rate law for this reaction is Rate = k [S-3-chloro-2-methylhexane]
CH3
H,C.
CH3
+ CEN
H2
The mechanism for this reaction is SN1
HC

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