Acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an El mechanism. The first step is the protonation of the alcohol oxygen to form an oxonium ion. Dehydration of 3-methyl-2-butanol forms one major and two minor organic products. Draw the structures, including hydrogen atoms, of the three organic products of this reaction. H. : OH major product minor product minor product H. H. 3-methyl-2-butanol an oxonium ion Draw the product. Draw minor product 1. Select Rings More Erase Select Draw Rings More Erase Draw H H

Acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an El mechanism. The first step is the protonation of the alcohol oxygen to form an oxonium ion. Dehydration of 3-methyl-2-butanol forms one major and two minor organic products. Draw the structures, including hydrogen atoms, of the three organic products of this reaction. H. : OH major product minor product minor product H. H. 3-methyl-2-butanol an oxonium ion Draw the product. Draw minor product 1. Select Rings More Erase Select Draw Rings More Erase Draw H H

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter8: Haloalkanes, Halogenation, And Radical Reactions

Section8.7: Radical Autoxidation

Problem CQ

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Acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an E1 mechanism. The first step is the protonation of the alcohol oxygen to form an oxonium ion. Dehydration of 3-methyl-2-butanol forms one major and two minor organic products. Draw the structures, including hydrogen atoms, of the three organic products of this reaction. н н :бн н Нас. Нас. CHз CH3 ČH3 CH3 3-methyl-2-butanol an oxonium ion Major Product Minor Product Minor Product
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