Question

when (z)-3-methylhex-3-ene undergoes hydroboration-oxidation, two isomeric products are formed. draw one of the products. draw the molecule on the canvas by choosing buttons from the tools (for bonds and charges), atoms, and templates toolbars. show the appropriate stereochemistry by choosing the dashed or wedged buttons and then clicking a bond on the canvas.

Answer 1

An alkene can become an alcohol through a two-step chemical process called hydroboration-oxidation. Borane (BH3) is added during the hydroboration process. Cyclohexanol is produced by the hydroboration-oxidation of cyclohexene.

How does the hydroboration-oxidation technique work?

In organic chemistry, the hydroboration-oxidation process is a two-stage hydration reaction that converts an alkene into alcohol. As a result, the hydroboration process transforms alkynes into aldehydes and alkenes into neutral alcohols.

Give an example of the hydroboration-oxidation reaction.

The addition of borane followed by oxidation is referred to as the hydroboration-oxidation reaction. For instance, the hydroboration-oxidation reaction of propene results in propan-1-ol. The addition product of this reaction between propene and diborane (BH3)2 is trialkyl borane.

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