The deuterated alcohol below can be converted to an alkyl halide via a mesylate intermediate. Complete the mechanism, draw the final product (with nonbonding electrons) and select the correct absolute stereochemistry of the starting material and the final product.

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter4: Organic Compounds: Cycloalkanes And Their Stereochemistry
Section4.SE: Something Extra
Problem 61AP: Ketones react with alcohols to yield products called acetals. Why does the all-cis isomer of...
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The deuterated alcohol below can be converted to an alkyl halide via a mesylate intermediate. Complete the mechanism,
draw the final product (with nonbonding electrons) and select the correct absolute stereochemistry of the starting material
and the final product.
Draw curved arrows to form the alkyl halide.
Select Draw
Rings
More
Erase
H
H3C-S-CI
:0 :
H
: C:
но
H
:0 :
H
What is the absolute configuration of the Cl carbon in the starting alcohol?
OS
OR
Draw the final product with stereochemistry and lone pairs. The leaving group has been pre-drawn for
your convenience.
Select
Draw
Rings
More
Erase
D
:0 :
:0 :
Transcribed Image Text:The deuterated alcohol below can be converted to an alkyl halide via a mesylate intermediate. Complete the mechanism, draw the final product (with nonbonding electrons) and select the correct absolute stereochemistry of the starting material and the final product. Draw curved arrows to form the alkyl halide. Select Draw Rings More Erase H H3C-S-CI :0 : H : C: но H :0 : H What is the absolute configuration of the Cl carbon in the starting alcohol? OS OR Draw the final product with stereochemistry and lone pairs. The leaving group has been pre-drawn for your convenience. Select Draw Rings More Erase D :0 : :0 :
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