Chemical Reactions of Haloarenes

Benzyl chloride  $\left(C_6{H}_{5}C{H}_{2}Cl\right)$ can be prepared from toluene by chlorination with –

The structure of the major organic product expected form the following reaction are

${\mathrm{C}}_6{\mathrm{H}}_{6 }\text{(Benzene)}+{\left({\mathrm{CH}}_3\right)}_2{\mathrm{CHCH}}_2\mathrm{Cl}\stackrel{{\mathrm{AlCl}}_3}{\to }$

In the following reaction, the nucleophile $(Me{O}^{⊝} )$ will displace which of the halogen atoms most readily?

Examine the structural formula shown below and find out how many compounds undergo electrophilic nitration more rapidly than fluoro benzene.

Assertion: In mono haloarenes, electrophilic substitution occurs at ortho and para positions.

Reason: Halogen atom is a ring deactivator.
 

Why does benzene undergo an electrophilic substitution reaction easily?

Explain electrophilic substitution reaction in haloarenes.

 Electrophilic substitution reactions of Haloarenes are

 Electrophilic substitution reactions of Haloarenes are meta directing.

 Electrophilic substitution reactions of Haloarenes are

Write the mechanism of the electrophilic substitution reaction of Haloarenes.

Presence of a nitro group at ortho or para position increases the reactivity of haloarenes towards _____  substitution.(nucleophilic/electrophilic)

The halogen compound which will not react with phenol to give ethers is

The halogen compound which will not react with phenol to give ethers is

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

follow the order:-

The major product of the following reaction is _________

In the questions arrange the compounds in increasing order of rate of reaction towards nucleophilic substitution.

The above reaction is an example of _____ reaction. (Wurtz/Fittig)

Aryl halides are less reactive towards nucleophilic substitution reaction as compared to alkyl halides due to: