The correct order of the electron-donating or withdrawing effect (inductive/mesomeric effect) for the groups $-NH_2, -OCH_3, -C_6H_5$,and $-NO_2$ is:

What are the characteristics of the inductive effect?

Which of the following orders of rotation barrier about the $C=C$ bond,as indicated in the structures $(I)$,$(II)$,and $(III)$,is correct?

Polarisation of electrons in acrolein may be written as:

Which one of the following is not true regarding electromeric effect?

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 $O^-$)