The following is a nucleophilic substitution reaction of R-3-chloro-2-methylhexane with "OCH3. The optical rotation of the solution after the reaction was complete was +11.4° CH3 Н. H,C. C' CH3 "OCH, + H2 H. The mechanism for this reaction is SN2 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 separate molecules/products.
The following is a nucleophilic substitution reaction of R-3-chloro-2-methylhexane with "OCH3. The optical rotation of the solution after the reaction was complete was +11.4° CH3 Н. H,C. C' CH3 "OCH, + H2 H. The mechanism for this reaction is SN2 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 separate molecules/products.
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
Chapter24: Catalytic Carbon-carbon Bond Formation
Section: Chapter Questions
Problem 24.8P
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