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Yes, sodium borohydride can reduce ketones.
Yes, sodium borohydride can reduce esters to alcohols.
No, sodium borohydride does not reduce carboxylic acids.
Yes, sodium borohydride can reduce esters to alcohols.
No, sodium borohydride cannot reduce carboxylic acids.
Yes, sodium borohydride can reduce ketones.
Yes, sodium borohydride can reduce esters to alcohols.
No, sodium borohydride does not reduce carboxylic acids.
Yes, sodium borohydride can reduce esters to alcohols.
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.
Lithium aluminum hydride is a stronger reducing agent compared to sodium borohydride. This means it can reduce a wider range of functional groups in organic compounds. Additionally, lithium aluminum hydride is more reactive and can be more difficult to handle safely compared to sodium borohydride.
Sodium borohydride is a base. It is an inorganic compound with the formula NaBH4 and is a white solid that is a reducing agent.It should NOT be confused withSodium bicarbonate, which is baking soda.