a. Draw the structures of all the elimination products. b. The reaction occurs through an E2 mechanism. Using one of your products write the mechanism of the reaction using curved arrows. c. Is this reaction regioselective? Explain your answer. d. Explain why the reaction is stereoselective.

a. Draw the structures of all the elimination products. b. The reaction occurs through an E2 mechanism. Using one of your products write the mechanism of the reaction using curved arrows. c. Is this reaction regioselective? Explain your answer. d. Explain why the reaction is stereoselective.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter22: Carbonyl Alpha-substitution Reactions

Section22.SE: Something Extra

Problem 48AP: How might you convert geraniol into either ethyl geranylacetate or geranylacetone?

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Question

a. Draw the structures of all the elimination products.

b. The reaction occurs through an E2 mechanism. Using one of your products write
the mechanism of the reaction using curved arrows.

c. Is this reaction regioselective? Explain your answer.

d. Explain why the reaction is stereoselective.

Consider the following elimination reaction below:
Br
KOCH2CH3
ethanol

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