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Does sodium borohydride reduce ketones?
Yes, sodium borohydride is commonly used as a reducing agent to reduce ketones to their respective alcohols.
What can sodium borohydride reduce in chemical reactions?
Sodium borohydride can reduce carbonyl compounds, such as aldehydes and ketones, in chemical reactions.
What can sodium borohydride (NaBH4) reduce?
Sodium borohydride (NaBH4) can reduce a variety of functional groups, including carbonyl compounds like aldehydes and ketones, as well as imines and Schiff bases.
Can sodium borohydride reduce esters?
Yes, sodium borohydride can reduce esters to alcohols.
Does sodium borohydride reduce carboxylic acids?
No, sodium borohydride does not reduce carboxylic acids.
Does sodium borohydride reduce ketones?
Yes, sodium borohydride is commonly used as a reducing agent to reduce ketones to their respective alcohols.
What can sodium borohydride reduce in chemical reactions?
Sodium borohydride can reduce carbonyl compounds, such as aldehydes and ketones, in chemical reactions.
What can sodium borohydride (NaBH4) reduce?
Sodium borohydride (NaBH4) can reduce a variety of functional groups, including carbonyl compounds like aldehydes and ketones, as well as imines and Schiff bases.
Can sodium borohydride reduce esters?
Yes, sodium borohydride can reduce esters to alcohols.
Does sodium borohydride reduce carboxylic acids?
No, sodium borohydride does not reduce carboxylic acids.
Does sodium borohydride reduce esters?
Yes, sodium borohydride can reduce esters to alcohols.
Can sodium borohydride reduce carboxylic acids?
No, sodium borohydride cannot reduce carboxylic acids.
Can sodium borohydride effectively reduce carboxylic acids?
Yes, sodium borohydride can effectively reduce carboxylic acids to alcohols.
Does sodium borohydride reduce alkenes?
Yes, sodium borohydride can reduce alkenes by adding hydrogen atoms to the carbon-carbon double bond, converting them into alkanes.
How is the reduction of ketones with sodium borohydride typically carried out in organic chemistry reactions?
In organic chemistry reactions, the reduction of ketones with sodium borohydride is typically carried out by adding the ketone to a solution of sodium borohydride in a suitable solvent, such as ethanol or methanol. The reaction is usually performed at room temperature or slightly elevated temperatures, and the resulting product is often isolated by simple workup procedures like filtration or evaporation.
How many moles required to reduce benzophenone to diphenylmethanol using sodium borohydride?
One mole of benzophenone requires one mole of sodium borohydride for reduction to diphenylmethanol.
Aldehydes and ketones may be reduced to?
Alcohols by using reducing agents such as sodium borohydride or lithium aluminum hydride in the presence of a solvent.
