Question:

What is the intermediate product obtained in the preparation of phenol from aniline?

Updated On: Apr 14, 2025
  • Sodium phenoxide
  • Benzene diazonium chloride
  • Anilinium cation
  • Benzene

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The Correct Option is B

Solution and Explanation

Correct Answer: Option 2 - Benzene diazonium chloride
The preparation of phenol from aniline involves a two-step chemical process, and the key intermediate formed during this reaction is benzene diazonium chloride.

Step 1: Diazotization of Aniline
• In the first step, aniline (C6H5NH2) is reacted with nitrous acid (HNO2) in the presence of hydrochloric acid (HCl) at low temperatures (0–5°C).
• Nitrous acid is usually generated in situ by reacting sodium nitrite (NaNO2) with dilute HCl.

The reaction is:
C6H5NH2 + HNO2 + HCl → C6H5N2Cl + 2H2O

• The compound formed here is benzene diazonium chloride, which is a stable intermediate only at low temperatures.

Step 2: Hydrolysis to form Phenol
• In the second step, this intermediate benzene diazonium chloride is heated with water (hydrolysis), often in the presence of dilute acids.
• This decomposes the diazonium salt and releases nitrogen gas (N2), forming phenol (C6H5OH) as the final product.

The reaction is:
C6H5N2Cl + H2O → C6H5OH + N2 + HCl

Conclusion:
The intermediate product formed during the conversion of aniline to phenol is benzene diazonium chloride. This compound plays a critical role in many substitution reactions in aromatic chemistry and is an essential intermediate in organic synthesis.

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