Diazonium Salts
CHXII13:AMINES

324282 The correct sequence of reactions to convert p-nitrophenol into quinol involves

1 reduction, diazotization and hydrolysis
2 hydrolysis, diazotization and reduction
3 hydrolysis, reduction and diazotization
4 diazotization, reduction and hydrolysis
CHXII13:AMINES

324283 In the sequence of following reactions:
supporting img

1 m-nitrotoluene
2 p-nitrotoluene
3 o- nitrotoluene
4 o-bromotoluene
CHXII13:AMINES

324284 The conversion of m-nitrophenol to resorcinol involves respectively

1 hydrolysis, diazotization and reduction
2 diazotization, reduction and hydrolysis
3 hydrolysis, reduction and diazotization
4 reduction, diazotization and hydrolysis
CHXII13:AMINES

324285 A compound \(X\) has the molecular formula \(\mathrm{C}_{7} \mathrm{H}_{7} \mathrm{NO}\). On treatment with \(\mathrm{Br}_{2}\) and \(\mathrm{KOH}, \mathrm{X}\) gives an amine \(\mathrm{Y}\). The latter gives carbylamine test. Y upon diazotisation and coupling with phenol gives an azo dye. Thus \(\mathrm{X}\) is

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COONH}_{4}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CONH}_{2}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{NO}\)
4 All of these
CHXII13:AMINES

324282 The correct sequence of reactions to convert p-nitrophenol into quinol involves

1 reduction, diazotization and hydrolysis
2 hydrolysis, diazotization and reduction
3 hydrolysis, reduction and diazotization
4 diazotization, reduction and hydrolysis
CHXII13:AMINES

324283 In the sequence of following reactions:
supporting img

1 m-nitrotoluene
2 p-nitrotoluene
3 o- nitrotoluene
4 o-bromotoluene
CHXII13:AMINES

324284 The conversion of m-nitrophenol to resorcinol involves respectively

1 hydrolysis, diazotization and reduction
2 diazotization, reduction and hydrolysis
3 hydrolysis, reduction and diazotization
4 reduction, diazotization and hydrolysis
CHXII13:AMINES

324285 A compound \(X\) has the molecular formula \(\mathrm{C}_{7} \mathrm{H}_{7} \mathrm{NO}\). On treatment with \(\mathrm{Br}_{2}\) and \(\mathrm{KOH}, \mathrm{X}\) gives an amine \(\mathrm{Y}\). The latter gives carbylamine test. Y upon diazotisation and coupling with phenol gives an azo dye. Thus \(\mathrm{X}\) is

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COONH}_{4}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CONH}_{2}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{NO}\)
4 All of these
NEET Test Series from KOTA - 10 Papers In MS WORD WhatsApp Here
CHXII13:AMINES

324282 The correct sequence of reactions to convert p-nitrophenol into quinol involves

1 reduction, diazotization and hydrolysis
2 hydrolysis, diazotization and reduction
3 hydrolysis, reduction and diazotization
4 diazotization, reduction and hydrolysis
CHXII13:AMINES

324283 In the sequence of following reactions:
supporting img

1 m-nitrotoluene
2 p-nitrotoluene
3 o- nitrotoluene
4 o-bromotoluene
CHXII13:AMINES

324284 The conversion of m-nitrophenol to resorcinol involves respectively

1 hydrolysis, diazotization and reduction
2 diazotization, reduction and hydrolysis
3 hydrolysis, reduction and diazotization
4 reduction, diazotization and hydrolysis
CHXII13:AMINES

324285 A compound \(X\) has the molecular formula \(\mathrm{C}_{7} \mathrm{H}_{7} \mathrm{NO}\). On treatment with \(\mathrm{Br}_{2}\) and \(\mathrm{KOH}, \mathrm{X}\) gives an amine \(\mathrm{Y}\). The latter gives carbylamine test. Y upon diazotisation and coupling with phenol gives an azo dye. Thus \(\mathrm{X}\) is

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COONH}_{4}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CONH}_{2}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{NO}\)
4 All of these
CHXII13:AMINES

324282 The correct sequence of reactions to convert p-nitrophenol into quinol involves

1 reduction, diazotization and hydrolysis
2 hydrolysis, diazotization and reduction
3 hydrolysis, reduction and diazotization
4 diazotization, reduction and hydrolysis
CHXII13:AMINES

324283 In the sequence of following reactions:
supporting img

1 m-nitrotoluene
2 p-nitrotoluene
3 o- nitrotoluene
4 o-bromotoluene
CHXII13:AMINES

324284 The conversion of m-nitrophenol to resorcinol involves respectively

1 hydrolysis, diazotization and reduction
2 diazotization, reduction and hydrolysis
3 hydrolysis, reduction and diazotization
4 reduction, diazotization and hydrolysis
CHXII13:AMINES

324285 A compound \(X\) has the molecular formula \(\mathrm{C}_{7} \mathrm{H}_{7} \mathrm{NO}\). On treatment with \(\mathrm{Br}_{2}\) and \(\mathrm{KOH}, \mathrm{X}\) gives an amine \(\mathrm{Y}\). The latter gives carbylamine test. Y upon diazotisation and coupling with phenol gives an azo dye. Thus \(\mathrm{X}\) is

1 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{COONH}_{4}\)
2 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CONH}_{2}\)
3 \(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{CH}_{2} \mathrm{NO}\)
4 All of these