Question:

The sequence of reagents required to convert benzoic acid to n-propyl benzene is

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Convert carboxylic acid to alkylbenzene: COOH $\to$ COCl $\to$ ketone $\to$ alkane. Use SOCl$_2$ for acid chloride, organocadmium for ketone, Clemmensen for reduction.
Updated On: Oct 27, 2025
  • SOCl$_2$, (C$_2$H$_5$)$_2$Cd, LiAlH$_4$
  • SOCl$_2$, (C$_2$H$_5$)$_2$Cd, Zn-Hg, HCl
  • SOCl$_2$, C$_2$H$_5$MgBr, Zn/H$^+$
  • HCl, C$_2$H$_5$MgBr, LiAlH$_4$
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The Correct Option is B

Solution and Explanation

1. Benzoic acid (C$_6$H$_5$COOH) to n-propylbenzene (C$_6$H$_5$CH$_2$CH$_2$CH$_3$).
2. Step 1: SOCl$_2$ converts COOH to COCl (benzoyl chloride).
3. Step 2: (C$_2$H$_5$)$_2$Cd reacts with COCl to form ketone C$_6$H$_5$COCH$_2$CH$_3$.
4. Step 3: Zn-Hg/HCl (Clemmensen reduction) reduces ketone to C$_6$H$_5$CH$_2$CH$_2$CH$_3$.
5. Other options: (1) LiAlH$_4$ reduces to alcohol; (3) Grignard gives tertiary alcohol; (4) HCl is ineffective.
6. Thus, the answer is (2) SOCl$_2$, (C$_2$H$_5$)$_2$Cd, Zn-Hg, HCl.
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