Yes, sodium borohydride can reduce esters to alcohols.
Yes, sodium borohydride can reduce esters to alcohols.
Yes, sodium borohydride can reduce ketones.
No, sodium borohydride does not reduce carboxylic acids.
No, sodium borohydride cannot reduce carboxylic acids.
Sodium borohydride can reduce carbonyl compounds, such as aldehydes and ketones, in chemical reactions.
Yes, sodium borohydride can reduce esters to alcohols.
Yes, sodium borohydride can reduce ketones.
No, sodium borohydride does not reduce carboxylic acids.
No, sodium borohydride cannot reduce carboxylic acids.
Sodium borohydride can reduce carbonyl compounds, such as aldehydes and ketones, in chemical reactions.
Yes, sodium borohydride can effectively reduce carboxylic acids to alcohols.
Yes, sodium borohydride is commonly used as a reducing agent to reduce ketones to their respective alcohols.
Yes, sodium borohydride can reduce alkenes by adding hydrogen atoms to the carbon-carbon double bond, converting them into alkanes.
Sodium borohydride (NaBH4) can reduce a variety of functional groups, including carbonyl compounds like aldehydes and ketones, as well as imines and Schiff bases.
One mole of benzophenone requires one mole of sodium borohydride for reduction to diphenylmethanol.
Yes, sodium borohydride is the same as sodium borohydride. It is a commonly used reducing agent in organic chemistry.
Yes, sodium borohydride is a reducing agent.