Which of the following is most reactive towards alkaline hydrolysis?

Give reasons:

The presence of the nitro group $\left(-{\mathrm{NO}}_2\right)$ at 0/p positions increases the reactivity of haloarenes towards nucleophilic substitution reactions.

The correct order of the following compounds showing increasing tendency towards nucleophilic substitution reaction is:

How will you bring about following conversions, toluene to benzyl alcohol?

The correct order of reactivity of following haloarenes towards nucleophilic substitution with aqueous $\mathrm{NaOH}$ is:

Choose the correct answer from the options given below:

Arrange the following compounds in incrensing order of their rate of reaction towards hydroxyl ion $\left({\mathrm{OH}}^{-}\right)$.

I 

II

III 

IV 

The product in the above reaction is

How will you convert the following ?

• Chlorobenzene to Aniline

Write the product formed when p-nitrochlorobenzene is heated with aqueous $\mathrm{NaOH}$ at 443 K followed by acidification.

The rates of reaction of $\mathrm{NaOH}$ with:

follow the order:-

Identify the relation among the rates of following nucleophilic substitution reactions?