What is meant by hydroboration oxidation reaction?
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In organic chemistry, the hydroboration–oxidation reaction is a two-step organic reaction that converts an alkene into a neutral alcohol by the net addition of water across the double bond.[1] The hydrogen and hydroxylgroup are added in a syn addition leading to cis stereochemistry. Hydroboration–oxidation is an anti-Markovnikov reaction, with the hydroxyl group attaching to the less-substituted carbon. The reaction was first reported by Herbert C. Brown in the late 1950s[2] and it was recognized in his receiving the Nobel Prize in Chemistry in 1979.
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The addition of diborane to alkenes to form trialkylboranes followed by their oxidation with alkaline hydrogen peroxide to form alcohols is called hydroboration-oxidation reaction.
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