The decreasing order of acidity of the following terminal acetylenes is:

The decreasing order of stability of the following anions 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

What is the inductive effect? Explain it in detail.

State True or False for the following statements:
$(i)$ The stability is explained by resonance effect and hyperconjugation.
$(ii)$ The resonance structures are drawn in resonance and hyperconjugation.
$(iii)$ Hyperconjugation is a bondless resonance.
$(iv)$ In resonance structure,there is movement of electron pair of only $\pi$ bond.

What is the effect of electron displacement in a covalent bond?