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Well, you have an acid and a base so the result would be a p-anisidine hydrochloride salt.

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10y ago
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3w ago

The reaction of p-anisidine with hydrochloric acid involves protonation of the nitrogen atom in the aniline ring to form a stable ammonium salt. This results in the formation of a water-soluble salt that can be isolated as a solid precipitate upon addition of a suitable base.

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Q: What is the reaction of p-anisidine with hydrochloric acid?
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