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
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter19: Aldehydes And Ketones: Nucleophilic Addition Reactions
Section19.SE: Something Extra
Problem 28VC
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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.
H3C.
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 HCl.
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.
Transcribed Image Text: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. H3C. 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 HCl. 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.
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