Why must dehydration reactions of alcohols be carried out under acid catalysis? 1) the hydroxide group is a poor leaving group and must be protonated to generate a better leaving group. 2) the hydroxide group is a great leaving group and does not need to be protonated to generate a better leaving group. 3) the acid isn't necessary for the reaction. 4) None of these are correct answers.

Introduction to General, Organic and Biochemistry
11th Edition
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Chapter14: Alcohols, Ethers, And Thiols
Section: Chapter Questions
Problem 14.71P: 14-71 The mechanism of the acid-catalyzed dehydration of an alcohol to an alkene is the reverse of...
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Why must dehydration reactions of alcohols be carried out under acid catalysis?
O 1) the hydroxide group is a poor leaving group and must be protonated to
1)
generate a better leaving group.
2) the hydroxide group is a great leaving group and does not need to be
protonated to generate a better leaving group.
O 3) the acid isn't necessary for the reaction.
O4)
None of these are correct answers.
Transcribed Image Text:Why must dehydration reactions of alcohols be carried out under acid catalysis? O 1) the hydroxide group is a poor leaving group and must be protonated to 1) generate a better leaving group. 2) the hydroxide group is a great leaving group and does not need to be protonated to generate a better leaving group. O 3) the acid isn't necessary for the reaction. O4) None of these are correct answers.
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