Answer:
Due
to -1 and- R-effect of the group,
electron density in the O?H bond decreases while due to +1 or hyper conjugation
effect, of the group, the
electron density in the O?H bond increases.
As a result, O?H bond is o-nitrophenol is much weaker than the O?H bond
is o-cresol and hence o-nitrophenol is much more acidic than o-cresol.
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