324317 Nitration of nitrobenzene is carried out. Then obtained product is reduced with \(\mathrm{Fe} / \mathrm{HCl}\), product so formed on reaction with \(\mathrm{HNO}_{2}\) and then with \(\mathrm{H}_{2} \mathrm{O}\), forms

324318 Nitrobenzene gives \(\mathrm{N}\)-phenylhydroxylamine by

324319 Assertion :
Nitroalkanes, but not nitroarenes can be distilled at normal atmospheric pressure.
Reason :
Nitroalkanes are sparingly soluble in water while nitroarenes are insoluble.

324320 Assertion :
Nitrobenzene undergoes electrophilic substitution at meta - position while nucleophilic substitution occurs at ortho - and para - positions.
Reason :
Nitro group in benzene ring significantly lowers the electron density at orthoand para - positions, while at meta - position, the electron density is only originally lowered.

324317 Nitration of nitrobenzene is carried out. Then obtained product is reduced with \(\mathrm{Fe} / \mathrm{HCl}\), product so formed on reaction with \(\mathrm{HNO}_{2}\) and then with \(\mathrm{H}_{2} \mathrm{O}\), forms

324318 Nitrobenzene gives \(\mathrm{N}\)-phenylhydroxylamine by

324319 Assertion :
Nitroalkanes, but not nitroarenes can be distilled at normal atmospheric pressure.
Reason :
Nitroalkanes are sparingly soluble in water while nitroarenes are insoluble.

324320 Assertion :
Nitrobenzene undergoes electrophilic substitution at meta - position while nucleophilic substitution occurs at ortho - and para - positions.
Reason :
Nitro group in benzene ring significantly lowers the electron density at orthoand para - positions, while at meta - position, the electron density is only originally lowered.

324317 Nitration of nitrobenzene is carried out. Then obtained product is reduced with \(\mathrm{Fe} / \mathrm{HCl}\), product so formed on reaction with \(\mathrm{HNO}_{2}\) and then with \(\mathrm{H}_{2} \mathrm{O}\), forms

324318 Nitrobenzene gives \(\mathrm{N}\)-phenylhydroxylamine by

324319 Assertion :
Nitroalkanes, but not nitroarenes can be distilled at normal atmospheric pressure.
Reason :
Nitroalkanes are sparingly soluble in water while nitroarenes are insoluble.

324320 Assertion :
Nitrobenzene undergoes electrophilic substitution at meta - position while nucleophilic substitution occurs at ortho - and para - positions.
Reason :
Nitro group in benzene ring significantly lowers the electron density at orthoand para - positions, while at meta - position, the electron density is only originally lowered.

324317 Nitration of nitrobenzene is carried out. Then obtained product is reduced with \(\mathrm{Fe} / \mathrm{HCl}\), product so formed on reaction with \(\mathrm{HNO}_{2}\) and then with \(\mathrm{H}_{2} \mathrm{O}\), forms

324318 Nitrobenzene gives \(\mathrm{N}\)-phenylhydroxylamine by

324319 Assertion :
Nitroalkanes, but not nitroarenes can be distilled at normal atmospheric pressure.
Reason :
Nitroalkanes are sparingly soluble in water while nitroarenes are insoluble.

324320 Assertion :
Nitrobenzene undergoes electrophilic substitution at meta - position while nucleophilic substitution occurs at ortho - and para - positions.
Reason :
Nitro group in benzene ring significantly lowers the electron density at orthoand para - positions, while at meta - position, the electron density is only originally lowered.