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.
<h3>How does the hydroboration-oxidation technique work?</h3>
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.
<h3>Give an example of the hydroboration-oxidation reaction.</h3>
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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1.) Moe will feel pain and he will see one side go to the right and disappear
<span>Nitrogen-14 should be the correct response.</span>
