The major aromatic product of the following reaction sequence is:

Given below are two statements:
Statement $I$: The acidic strength of monosubstituted nitrophenol is higher than phenol because of the electron-withdrawing nitro group.
Statement $II$: $o$-nitrophenol,$m$-nitrophenol,and $p$-nitrophenol will have the same acidic strength as they have one nitro group attached to the phenolic ring.
In the light of the above statements,choose the most appropriate answer from the options given below:

Which of the following reactions will form a tri-bromo derivative of phenol?

Which of the following substances will increase the acidity of phenol?

When phenol reacts with ammonia in the presence of $ZnCl_2$ at $300 \ ^oC$,it gives:

The correct sequence of reactions to convert $p$-nitrophenol into quinol involves