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Base hydrolysis splits at the peptide link - giving sodium ethanoate and 4-aminophenol, but then the phenol group itself loses a proton, so that becomes 4-amino sodium phenoxide.

This was Q2 cii on F324 Jan 2012 - the examiners regarded this as a high demand question.

Acid hydrolysis will give you the carboxylic acid and the aminophenol will be protonated as NH3+. Check out Chemguide.

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