The correct stability order of the following species/molecules is:

Match column $-I$ and column $-II$ with the correct electronic effect relation:

Column $-I$	Column $-II$
$(i)$ $C_6H_5NH_2$	$(p)$ $-R$ effect
$(ii)$ $C_6H_5OH$	$(q)$ $+R$ effect
$(iii)$ $C_6H_5NO_2$	$(r)$ $+I$ effect
$(iv)$ $CH_3CH_2Cl$	$(s)$ $-I$ effect

State True or False for the following statements:
$(i)$ The stability of carbocation is explained by the delocalized structure of hyperconjugation.
$(ii)$ The stability of carbocation is explained by drawing the resonance structure.
$(iii)$ Hyperconjugation effect is $(+)$ or $(-)$.
$(iv)$ Mesomeric effect is $(+)$ or $(-)$.

Arrange the following compounds in increasing order of the rate of aromatic electrophilic substitution reaction:

Match the following electronic effects in List-$I$ with their corresponding examples or representations in List-$II$.

List-$I$	List-$II$
$(A)$ Resonance	$(I)$ $C=C + H^+ \rightarrow C^+-C-H$
$(B)$ Inductive effect	$(II)$ $H-CH_2-CH_2^+ \leftrightarrow H-CH_2=CH_2^+$
$(C)$ Electromeric effect	$(III)$ $C_6H_6$
$(D)$ Hyperconjugation	$(IV)$ $CH_3-Z \rightarrow CH_3^- + Z^+$
	$(V)$ $CH_3-CH_2-CH_2Cl$

Steric inhibition of resonance takes place in