Arrange the following compounds in decreasing order of reactivity towards $EAS$ (electrophilic aromatic substitution).

Arrange the following according to the instructions:
$(i)$ Arrange in descending order of acidic strength:
$CH_3COOH, (CH_3)_3CCOOH, (CH_3)_2CHCOOH, CH_3CH_2COOH$
(ii) Arrange in descending order of stability:
$\stackrel{+}{CH}_3, (CH_3)_3\stackrel{+}{C}, CH_3CH_2^+, (CH_3)_2\stackrel{+}{CH}$
(iii) Arrange in increasing order of acidic strength:
$CCl_3COOH, CH_3COOH, CHCl_2COOH, CH_2ClCOOH$
(iv) Arrange in increasing order of stability:
$(a)$ $CH_3CH=CH-CHO$
$(b)$ $CH_3\stackrel{+}{CH}-CH=C-O:^-$
$(c)$ $\stackrel{+}{CH}_2-CH=CH-C=O$
$(v)$ Arrange in decreasing order of stability:
$(I)$ $CH_2=CH-CHO$
$(II)$ $\stackrel{+}{CH}_2-CH=C-H$ (with $O^-$)
$(III)$ $:CH_2-CH=C-H$ (with $O^-$)

Which of the following statements are correct?
$(i)$ Inductive effect and resonance effect are possible in chlorobenzene.
$(ii)$ Resonance effect dominates over inductive effect in anisole.
$(iii)$ $p-$nitrobenzoic acid is less acidic than $m-$nitrobenzoic acid.
$(iv)$ Diphenylamine is more basic than aniline.

Chloroacetic acid is a stronger acid than acetic acid. This can be explained using

The electron displacement in a covalent bond of a molecule is produced by which type of effects?

Which of the following is correct?