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

Macroscale and Microscale Organic Experiments
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Chapter19: Alkenes From Alcohols: Cyclohexene From Cyclohexanol
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Answer is two minor and one major product 

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
H.
major product
minor product
minor product
H.
H.
H.
3-methyl-2-butanol
an oxonium ion
Draw the major product.
Draw minor product 1.
Select
Draw
Rings
More
Erase
Select
Draw
Rings
More
Erase
H
:O:
Transcribed Image Text: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 H. major product minor product minor product H. H. H. 3-methyl-2-butanol an oxonium ion Draw the major product. Draw minor product 1. Select Draw Rings More Erase Select Draw Rings More Erase H :O:
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