Consider this two-step synthesis. Predict the product for each step, carefully considering bothstereo- and regioselectivity.step 1step 2NalEtO Na+аcetoneELOH, heatBrUsing a clearly drawn Newman projection (looking down the C2-C3 bond), show thestereochemical preference for step 2 in thespacebelow.

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Answered: Nal EtO Na+ acetone ELOH, heat Br

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Nal EtO Na+ acetone ELOH, heat Br

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter11: Reactions Of Alkyl Halides: Nucleophilic Substitutions And Eliminations

Section11.SE: Something Extra

Problem 37MP

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Question

Consider this two-step synthesis. Predict the product for each step, carefully considering both
stereo- and regioselectivity.
step 1
step 2
Nal
EtO Na+
аcetone
ELOH, heat
Br
Using a clearly drawn Newman projection (looking down the C2-C3 bond), show the
stereochemical preference for step 2 in the
space
below.

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