he following is a nucleophilic substitution reaction of S-3-chloro-2-methylhexane with CN. he experimental rate law for this reaction is Rate k [S-3-chloro-2-methylhexane] CH3 ,C. CH3 CEN H2 The mechanism for this reaction is Sy1 Draw the organic molecule(s) which is(are) formed in this reaction. Do not include molecules like H,O or HCI. Draw the specific configuration (R or S) at any chiral carbons within your product(s). If both configurations are formed in the product(s), draw both as
he following is a nucleophilic substitution reaction of S-3-chloro-2-methylhexane with CN. he experimental rate law for this reaction is Rate k [S-3-chloro-2-methylhexane] CH3 ,C. CH3 CEN H2 The mechanism for this reaction is Sy1 Draw the organic molecule(s) which is(are) formed in this reaction. Do not include molecules like H,O or HCI. Draw the specific configuration (R or S) at any chiral carbons within your product(s). If both configurations are formed in the product(s), draw both as
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
Chapter8: Haloalkanes, Halogenation, And Radical Reactions
Section: Chapter Questions
Problem 8.21P
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