It is impossible to synthesize diphenyl ether () using the Williamson ether synthesis. Which stateme — Alcohols Phenols and Ethers Chemistry Question

💡 Solution & Explanation

The Williamson synthesis requires the nucleophile to displace a halogen. Aryl halides are highly resistant to standard nucleophilic substitution ($S_NAr$) because resonance gives the $C-X$ bond partial double bond character, preventing the $S_N2$ attack.