Hydroboration & Oxidation of Alkenes


Hey organic chemistry learners! Here is a little something to help you remember the hydroboration & oxidation of alkenes which is considered as a bit tricky to remember.

Here first, BH3 & THF are added and then a intermediate with -BH2 is formed. Afterwards upon adding H2O2 with NaOH the -BH2 is replaced by an -OH group. BOOM! You have an alcohol.

This reaction gives higher yield of alcohols than alkenes’ reaction with H3O+. And no carbocation rearrangements happens. So this reaction is favored in synthesis of alcohols.

And remember this! It gives an anti-Markonikov, syn product!

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