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<p>to react with the alcohol. However <a href="page.php?w=phenols">phenols</a> can be used to replace the alcohol while maintaining the alkyl halide. Since phenols are acidic, they readily react with a strong <a href="page.php?w=Base_%28chemistry%29">base</a> like <a href="page.php?w=sodium_hydroxide">sodium hydroxide</a> to form phenoxide ions. The phenoxide ion will then substitute the -X group in the alkyl halide, forming an ether with an aryl group attached to it in a reaction with an <a href="page.php?w=SN2">S<sub>N</sub>2</a> mechanism.</p>

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