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it should be pretty stable... if I were forced to hazard a guess though, then 3-methyl-2-butanol would be really the only solution. The lone pair of the OH2 attacks the bond, then a H+ goes in and attacks the more substituted carbon (which used to be the 2-methyl one, and is now the 3-methyl one)

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16y ago

What else can I help you with?