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Consider the acid-catalyzed hydration of 3-methyl-1-butene. For each of the four steps, add one or two curved arrows to the reactant side to show the mechanism.

Answer :

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Answer:

This addition follows MarkowniKov's rule

Explanation:

The image attached shows the mechanism of the reaction. It can easily be seen that a secondary carbocation is formed leading to the alkanol. The image simplifies the mechanism which involves the initial addition of the hydroxide followed by the hydrogen ion.

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