Question:

Williamson synthesis is an example of:

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Williamson synthesis: Alkoxide (nucleophile) + Alkyl halide ? Ether. Always use primary alkyl halide to avoid elimination.
Updated On: Jul 23, 2026
  • Nucleophilic addition reaction
  • Electrophilic substitution reaction
  • Nucleophilic substitution reaction
  • Electrophilic addition reaction
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The Correct Option is C

Solution and Explanation

Step 1: Concept
Williamson synthesis is the industrial and laboratory method for preparing ethers.

Step 2: Analysis
In this reaction, a sodium alkoxide ($R-O^-Na^+$) reacts with an alkyl halide ($R'-X$). The alkoxide ion ($R-O^-$) is a strong nucleophile that attacks the electrophilic carbon bearing the halogen. The halide ion is displaced as a leaving group.

Step 3: Conclusion
This is a classic $S_N2$ mechanism -- a nucleophilic species substitutes a leaving group -- making it a nucleophilic substitution reaction. The reaction: $R-ONa + R'-X \rightarrow R-O-R' + NaX$.

Final Answer: (C)
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