2-methyl-2-hexanol was prepared by reacting an alkene with either hydroboration-oxidation or oxymercuration-reduction. Draw the structure of the alkene that was used to prepare the alcohol in highest yield. You do not have to consider stereochemistry.

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Explanation:

In this question, we have to synthesize a molecule in which the "OH" group is placed in the most substituted carbon. Therefore we have to use a markovnikov reaction to the synthesis. The hydroboration is anti-markovnikov and the oxymercuration-reduction is markovnikov, therefore the oxymercuration-reduction is our best choice.

Now, the double bond can be placed in different places. Because the "OH" would be added in the tertiary carbon of the double bond. So, we can use 2-methylhex-1-ene or 2-methylhex-2-ene.

See figure 1.

I hope it helps

kuchisake

kuchisake-onna (口裂け女, "slit mouth woman ") is a malevolent figure appearing in japanese ghost stories, possibly dating back to the edo period. she takes the form of a masked woman who approaches people and asks them if they believe she is pretty.

explanation: