. 1-methylcyclopentanol reacts with HBr to give the corresponding alkyl bromide via a carbocation intermediate. Draw the carbocation intermediate. Is this a primary, secondary or tertiary carbocation?

. 1-methylcyclopentanol reacts with HBr to give the corresponding alkyl bromide via a carbocation intermediate. Draw the carbocation intermediate. Is this a primary, secondary or tertiary carbocation?

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter5: Stereochemistry At Tetrahedral Centers

Section5.SE: Something Extra

Problem 75AP

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The acid HBr gives H⁺which protonates the alcohol -OH to ⁺OH₂ .
This then leaves as a water molecule, leaving behind a carbocation.

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