What happens when carbonyl compounds are treated with hydrazine? Write the reaction.
Answer
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Hint :Carbonyl compounds are the compounds having a carbonyl group attached to the molecule. A carbonyl carbon is a functional group in which a carbon atom is double bonded to the oxygen and the general carbonyl compound is represented as $ R - C(R) = O $ .
Complete Step By Step Answer:
First of all, we start with what is hydrazine.
Hydrazine: Hydrazine is an alkaline liquid which is a very powerful reducing agent having the chemical formula $ N{H_2} - N{H_2} $ .
Carbonyl compounds: The organic compounds aldehyde and ketones are carbonyl compounds, as have carbonyl groups.
Now, we will treat carbonyl compounds with the hydrazine.
The reaction of carbonyl compounds with the hydrazine:
First of all, the carbonyl group is reacted with hydrazine. This forms hydrazone.
When the medium is basic. The terminal nitrogen atom of the hydrazone is deprotonated and makes double bonds with the neighbouring nitrogen. The proton which is released is attached to hydroxide ion to form water. As oxygen is more electron withdrawing than carbon, the carbon is protonated by the water. The terminal nitrogen is deprotonated again and the triple bond with the nitrogen atom at the neighbour which forms carbanion. Another proton forms water from the environment which is basic. Then, the carbonyl compound is converted into alkane.
Hence, the complete reaction is as follows:
The reaction is also known as Wolf-Kishner reduction. In these reactions, carbonyl carbon is reduced to alkane.
Note :
There are various other methods to convert carbonyl compounds to alkanes like Clemmensen reduction in which the carbonyl is reacted with zinc amalgam in presence of aqueous hydrochloric acid.
Complete Step By Step Answer:
First of all, we start with what is hydrazine.
Hydrazine: Hydrazine is an alkaline liquid which is a very powerful reducing agent having the chemical formula $ N{H_2} - N{H_2} $ .
Carbonyl compounds: The organic compounds aldehyde and ketones are carbonyl compounds, as have carbonyl groups.
Now, we will treat carbonyl compounds with the hydrazine.
The reaction of carbonyl compounds with the hydrazine:
First of all, the carbonyl group is reacted with hydrazine. This forms hydrazone.
When the medium is basic. The terminal nitrogen atom of the hydrazone is deprotonated and makes double bonds with the neighbouring nitrogen. The proton which is released is attached to hydroxide ion to form water. As oxygen is more electron withdrawing than carbon, the carbon is protonated by the water. The terminal nitrogen is deprotonated again and the triple bond with the nitrogen atom at the neighbour which forms carbanion. Another proton forms water from the environment which is basic. Then, the carbonyl compound is converted into alkane.
Hence, the complete reaction is as follows:
The reaction is also known as Wolf-Kishner reduction. In these reactions, carbonyl carbon is reduced to alkane.
Note :
There are various other methods to convert carbonyl compounds to alkanes like Clemmensen reduction in which the carbonyl is reacted with zinc amalgam in presence of aqueous hydrochloric acid.
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