In the acid-catalyzed dehydration of 2-methyl-1-propanol, what carbocation would be formed if a hydride shift accompanied cleavage of the carbon-oxygen bond in the alkyloxonium ion? What ion would be formed as a result of a methyl shift?

In the acid-catalyzed dehydration of 2-methyl-1-propanol, what carbocation would be formed if a hydride shift accompanied cleavage of the carbon-oxygen bond in the alkyloxonium ion? What ion would be formed as a result of a methyl shift?

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 72AP: Treatment of 1-bromo-2-deuterio-2-phenylethane with strong base leads to a mixture of deuterated and...

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Be sure to answer all parts.
In the acid-catalyzed dehydration of 2-methyl-1-propanol, what carbocation would be formed if a
hydride shift accompanied cleavage of the carbon-oxygen bond in the alkyloxonium ion?
What ion would be formed as a result of a methyl shift?
L

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