Concept:
Aldehydes and ketones undergo
nucleophilic addition–elimination reactions with ammonia derivatives of the type \(NH_2-G\).
In these reactions, the nucleophile attacks the carbonyl carbon, followed by the elimination of a water molecule, forming a compound containing a \(C=N-G\) linkage.
Step 1: {Identify the reacting reagent.}
The given reagent is
hydrazine \((H_2N-NH_2)\), which is an ammonia derivative.
Step 2: {Write the general reaction.}
Ketones react with hydrazine in the presence of acid catalyst to form hydrazone:
\[
R_2C=O + H_2N-NH_2 \xrightarrow{H^+} R_2C=N-NH_2 + H_2O
\]
In this reaction:
- The nucleophile \(H_2N-NH_2\) attacks the carbonyl carbon.
- A molecule of water is eliminated.
- A double bond \(C=N\) is formed.
Step 3: {Name the product.}
When the group \(G = -NH_2\) (from hydrazine), the product formed is called a
hydrazone.
Step 4: {Conclusion.}
Therefore, the product formed in this reaction is:
\[
\text{Hydrazone}
\]