Please answer this question: Congratulations on your internship at the ACME Chem

Question

Please answer this question: Congratulations on your internship at the ACME Chemical Co.! Your first assignment is to make the alcohol on the right from the bromide starting material. "Just mix it up with some water and a little HBr" says your supervisor. Are they wrong or right???? Do you have a better suggestion?

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Explanation / Answer

A) The alcohol that forms the most stablecarbocation will react fastest1-methylcyclohexanol (3y) > cyclohexanol(2y) >1-hexanol (1y)B) The carbocation intermediate is planar, and the halide may beintroduced above or below the plane ofthe carbocation. ? Regardless of whether westart with a racemic mixture or a pure enatiomer, the end productwill always yield a racemicmix. To avoid this, you must use reagents that do not undergoSn1.C) PBr3 or PCl3, SOCl2/Pyridine,HBr/H2SO4/? (mainl

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