Question

Which of the following statements is/ are true?
(I) Ethers are soluble in conc. $H_{2}S{O}_4$ but separate out on addition of water
(II) Ethers are used as solvents for $B{F}_3$ and Grignard reagent
(III) Mononitration of $p$-methylanisole gives $2$-nitro-$4$ methylanisole
(IV) Monobromination of $p$-ethoxyphenol gives $2$-bromo-$4$-ethoxyphenol
(V) $4$-Chlorophenol (I) will dissolve in $NaOH$ but $4$-chloro-$1$ -methyl benzene (II) will not
(VI) $4$-Methyl benzoic (III) acid will dissolve in aq. $NaHC{O}_3$ but $4$-methyl phenol (IV) will not
(VII) $2,4,6$-Trinitrophenol (V) will dissolve in aq. $NaHC{O}_3$ but $4$-methyl phenol (VI) will not
(VIII) $4$ -Ethyl phenol (VII) will dissolve in aq. $NaOH$ but ethyl phenyl ether (VIII) will not

Answer 1

Answer: 8

(I) Water is stronger base than ether and removes proton from protonated ether, $R_{2}O{H}^{+}$
$\underset{{\text{Acid}}_1}{[R_{2}OH{]}^{+}}$+ $\underset{\text{Base2}}{H_{2}O}$ $\to$ $\underset{\text{Base1}}{R_{2}O}$+$\underset{\text{Acid2}}{H_3{O}^{+}}$
(II) Due to unshared electron pairs, ethers act as Lewis bases and hence easily react with Lewis acids like $B{F}_3$ and $RMgBr$ to form coordinated compounds.

Note that two molecules of ether coordinate tetrahedrally with one $M{g}^{2+}$
(III)
(IV)
(V) Due to -$I$ effect of $Cl$, $4$ -chlorophenol is acidic and dissolves in $NaOH$, but (II) is an aryl halide and does not dissolve
(VI) (III) is an acid and dissolves in $NaHC{O}_3$ but (IV) is a phenol and does not dissolve
(VII) Although (V) is a phenol, because of the presence of $(3N{O}_2)$ group, it is exceptionally acidic $(p{k}_a=0.38)$ So it dissolves in $NaHC{O}_3$ but (VI) is a phenol $(p{K}_a=10.17)$ and will not dissolve
(VIII) (VII) is a phenol and dissolves in NaOH, but (VIII) is an ether; and does not dissolve.