Give a structural formula for the carbocation intermediate that leads to the major product in each of the reactions of Problem 6.4.
Sample Solution (a) Protonation of the double bond of 2-methyl-2-butene can give a tertiary carbocation or a secondary carbocation.
The product of the reaction is derived from the more stable carbocation—in this case, it is a tertiary carbocation that is formed more rapidly than a secondary one.
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