Acid-catalyzed addition of water to an alkene yields an alcohol with markovnikov regiochemistry. the electrophilic h+ adds to the sp2 carbon with the most hydrogens to yield the most stable carbocation intermediate, which then adds water to give the product alcohol. because a carbocation intermediate is formed, rearrangements can occur prior to the addition of water.
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Acid-catalyzed addition of water to an alkene yields an alcohol with markovnikov regiochemistry. the...
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