Solution : Thinking process This problem is based on the acidic character of phenol. Electron - withdrawing group at $$o$$ and $$p$$ - position $$w.r.t.$$ $$-OH$$ group of Phenol, increase the acidic strength.
Picric acid ( 2, 4, 6 - trinitrophenol ) is extremely more acidic than given compounds because its $$pKa$$ value is close to zero also due to the presence of three strong electron withdrawing group ( $${ - N{O_2}}$$ group ) at $$ortho$$ and $$para$$ - positions, picric is more acidic compound.
Releted MCQ Question on Organic Chemistry >> Alcohol, Phenol and Ether
Releted Question 1
Ethyl alcohol is heated with conc $${H_2}S{O_4}$$ the product formed is
A.
\[{{H}_{3}}C\underset{\begin{smallmatrix}
\parallel \\
O
\end{smallmatrix}}{\mathop{-C-}}\,O{{C}_{2}}{{H}_{5}}\]