Haloalkanes and Haloarenes
In Friedel craft alkylation of benzene with methyl chloride, the catalyst used is:
In which of the following reactions, the correct major product formed?
$$(A)$$ The reaction is Friedel craft's alkylation reaction. The isopropyl group enters ortho to the$$ -OH$$ group.
$$(B)$$ The reaction is Friedel craft's acylation reaction. The acetyl group enters ortho to the methyl group.
$$(C)$$ The $$H$$ atoms of the aromatic ring are replaced with $$Br$$ atoms to form tribromo derivative. Bromine enters at ortho and para position to amino group. This reaction occurs in presence of polar solvent such as water.
$$(D)$$ In presence of non polar solvent such as $$CS_2$$, the bromination of phenol gives ortho and para bromo phenol in the ratio $$1: 4$$.
In Friedel craft alkylation of benzene with methyl chloride, the catalyst used is:
The reaction of toluene with chlorine in the presence of ferric chloride gives predominantly:
Chlorobenzene is formed by reaction of chlorine with benzene in the presence of $$A1C1_3$$.Which of the following species attacks the benzene ring in this reaction?
Chloroform on treatment with phenol in presence of caustic alkali forms salicylaldehyde. This reaction is known as:
Benzene reacts with $$CH_{3}Cl$$ in the presence of anhydrous $$AlCl_{3}$$ to form:
The compound $$C_{7}H_{8}$$ undergoes the following reactions: $$C_{7}H_{8}\xrightarrow {3Cl_{2}/\triangle}A \xrightarrow {Br_{2}/ Fe} B \xrightarrow {Zn/HCl}C$$. The product $$C$$ is:
Among the following, the reaction that proceeds through an electrophilic substitution is:
On commercial scale, phenol is obtained from chlorobenzene. The chlorobenzene needed for the purpose is prepared by:
The product on monobromination of this compound is :
When phenol is treated with excess bromine water, it gives: