Which of the following is the most correct electron displacement for a nucleophilic reaction to take place? 

1.
2.
3.
4.

Which of the following meta-directing substituents is the most deactivating in aromatic substitution?

Among the following compounds the one that is most reactive towards electrophilic nitration is:
1. Benzoic acid
2. Nitrobenzene
3. Toluene
4. Benzene

Among cyclohexanol (I), acetic acid (II), 2, 4, 6-trinitrophenol (III) and phenol (IV) the correct order of decreasing acidic character will be:

Which one is most reactive towards S_N1 reaction?

1. $C_6{H}_{5}CH\left(C_6{H}_5\right)Br$

2. $C_6{H}_{5}CH\left(C{H}_3\right)Br$

3. $C_6{H}_{5}C\left(C{H}_3\right)\left(C_6{H}_5\right)Br$

4. $C_6{H}_{5}C{H}_{2}Br$

Which one of the following is most reactive towards electrophilic attack?
 

1.		2.
3.		4.

In a S_N2 substitution reaction of the type 
$\mathrm{R}-\mathrm{Br}+\mathrm{Cl}^{-} \xrightarrow{\mathrm{DMF}} \mathrm{R}-\mathrm{Cl}+\mathrm{Br}^{-}$

one of the following that has the highest relative rate is:
 

1.	$\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{CH}_2 \mathrm{Br}$	2.
3.		4.	$\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{Br}$

For the above-given reaction, A (Predominantly) is:

1.		2.
3.		4.