e. Of the three compounds shown below, Compound A does not undergo E2 elimination, Compound B provides a chiral product upon E2 elimination, and Compound C yields a racemic product. Label these compounds A, B, or C in the boxes provided below and provide a justification for your choice in 1-2 sentences each. Br Br Br

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter22: Carbonyl Alpha-substitution Reactions
Section22.SE: Something Extra
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e. Of the three compounds shown below, Compound A does not undergo E2
elimination, Compound B provides a chiral product upon E2 elimination, and
Compound C yields a racemic product. Label these compounds A, B, or C in the
boxes provided below and provide a justification for your choice in 1-2 sentences
each.
Br
Br
Br
4. Retrosynthesis: Provide a forward synthesis of the following ketoaldehyde starting
from methylcyclopentane. Show reagents for each step. Include structures of
products that can be isolated after each step. Note: Do not provide a mechanism for any
step.
H
Transcribed Image Text:e. Of the three compounds shown below, Compound A does not undergo E2 elimination, Compound B provides a chiral product upon E2 elimination, and Compound C yields a racemic product. Label these compounds A, B, or C in the boxes provided below and provide a justification for your choice in 1-2 sentences each. Br Br Br 4. Retrosynthesis: Provide a forward synthesis of the following ketoaldehyde starting from methylcyclopentane. Show reagents for each step. Include structures of products that can be isolated after each step. Note: Do not provide a mechanism for any step. H
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