In the reaction of $1$-vinyl-$-2$-bromoethylbenzene with $HBr$,the major product is:

Arrange the following compounds in order of decreasing rate of hydrolysis for $SN_1$ reaction:
$(I)$ $C_6H_5CH_2Br$
$(II)$ $p-CH_3-C_6H_4-CH_2Br$
$(III)$ $p-(CH_3)_2CH-C_6H_4-CH_2Br$
$(IV)$ $p-CH_3CH_2-C_6H_4-CH_2Br$

Which compounds give $\beta$-elimination reactions? What are their main products?

In the given pair of compounds,in which pair is the second compound more reactive than the first toward $S_N2$ reaction?

Two isomers $(A)$ and $(B)$ with molar mass $184 \ g/mol$ and elemental composition $C, 52.2 \ \%; H, 4.9 \ \%$ and $Br, 42.9 \ \%$ give benzoic acid and $p$-bromobenzoic acid,respectively,on oxidation with $KMnO_4$. Isomer '$A$' is optically active and gives a pale yellow precipitate when warmed with alcoholic $AgNO_3$. Isomer '$A$' and '$B$' are,respectively .... .

Identify the correct reactivity order for $S_N1$ reaction for the following compounds: