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Reduction of nitrobenzene in the presenc...

Reduction of nitrobenzene in the presence of `Zn//NH_(4)Cl` gives

A

Aniline

B

Nitrosobenzene

C

hydrazobenzne

D

phenyl hydroxyl amine

Text Solution

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The correct Answer is:
To solve the question regarding the reduction of nitrobenzene in the presence of Zn/NH₄Cl, we can follow these steps: ### Step 1: Identify the Reactant The reactant in this reaction is nitrobenzene. The chemical structure of nitrobenzene is represented as: \[ \text{C}_6\text{H}_5\text{NO}_2 \] This indicates a benzene ring (C₆H₅) with a nitro group (NO₂) attached to it. **Hint:** Remember that nitrobenzene contains a nitro group which is a strong electron-withdrawing group. ### Step 2: Understand the Reducing Agent The reducing agent in this reaction is zinc (Zn) in the presence of ammonium chloride (NH₄Cl). Zinc provides nascent hydrogen, which is essential for the reduction process. **Hint:** Reducing agents donate electrons or hydrogen, facilitating the conversion of functional groups. ### Step 3: Reduction Reaction The reduction of nitrobenzene involves the conversion of the nitro group (NO₂) to a hydroxylamine group (NH₂OH). The reaction can be summarized as follows: \[ \text{C}_6\text{H}_5\text{NO}_2 + \text{Zn} + \text{NH}_4\text{Cl} \rightarrow \text{C}_6\text{H}_5\text{NHOH} + \text{by-products} \] The product formed is N-phenylhydroxylamine, which can be represented as: \[ \text{C}_6\text{H}_5\text{NHOH} \] **Hint:** The nitro group is reduced to a hydroxylamine group, which is characterized by the presence of both nitrogen and hydroxyl (OH) functional groups. ### Step 4: Final Product Identification The final product of this reduction reaction is N-phenylhydroxylamine. The structure of N-phenylhydroxylamine can be depicted as: \[ \text{C}_6\text{H}_5\text{NHOH} \] **Hint:** The name of the product reflects the presence of the phenyl group (from benzene) and the hydroxylamine functional group. ### Conclusion Thus, the reduction of nitrobenzene in the presence of Zn/NH₄Cl gives N-phenylhydroxylamine. **Final Answer:** N-Phenylhydroxylamine (Option D).
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