The correct option is
B B
The acidity of the compounds depends on stability of conjugate base formed .
The conjugate bases formed are :
At, ortho and para position, predominant effect of
−NO2is
−M effect,whereas at meta position , it shows
−I effect.
Also,
−CH3 when attached at para position shows predominantly
+H effect .
+H effect destabilizes the negative charge, whereas the conjugate base is stabilized by
−M and
−I effect of
−NO2 group.
More the nitro groups attached , more is the stability of conjugate base.
So, B is the most stable conjugate base formed, and hence the most acidic.