Question:

The reagent used in Sandmeyer reaction for converting benzene diazonium chloride into chlorobenzene is:

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Sandmeyer reactions use cuprous salts: \[ CuCl,\ CuBr,\ CuCN \] to replace diazonium groups with halogens or cyanide.
Updated On: May 31, 2026
  • \( CuCl/HCl \)
  • \( NaCl \)
  • \( Cl_2/FeCl_3 \)
  • \( SOCl_2 \)
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The Correct Option is A

Solution and Explanation

Concept:
Sandmeyer reaction is an important substitution reaction of diazonium salts where the diazonium group is replaced by halogens or cyanide using cuprous salts. General reaction: \[ ArN_2^+Cl^- \xrightarrow{CuX} ArX \] where: \[ X = Cl,\ Br,\ CN \]

Step 1:
Write the given transformation.
Benzene diazonium chloride: \[ C_6H_5N_2^+Cl^- \] must be converted into chlorobenzene: \[ C_6H_5Cl \]

Step 2:
Identify appropriate Sandmeyer reagent.
For replacement by chlorine: \[ CuCl/HCl \] is used. Reaction: \[ C_6H_5N_2^+Cl^- \xrightarrow{CuCl/HCl} C_6H_5Cl + N_2 \] Nitrogen gas escapes, driving the reaction forward.

Step 3:
Analyze incorrect options.

• \( NaCl \) cannot replace diazonium group.
• \( Cl_2/FeCl_3 \) is used for electrophilic chlorination.
• \( SOCl_2 \) converts alcohols into alkyl chlorides. Therefore the correct reagent is: \[ \boxed{CuCl/HCl} \]
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