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Phenol (without 'trinitro') is already a weak acid: Its Phe-OH group is protolised in water (= deprotonated), pKa=9.89, a very weak acid.

Phe-OH + H2O <--> Phe-O- + H3O+

In 2,4,6-trinitrophenol the acidity is very much stimulated by the presence of these 3 nitrogroups in ortho and para position. pKa=0.38, almost a strong acid.

(This can be explained by socalled resonance structure stabilisation of the picrate ion, (NO2)3Phe-O- , but this is far beyond the scope of this question).

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