Advertisements
Advertisements
Question
How will you convert nitrobenzene into o and p-nitrophenol?
Advertisements
Solution
Conversion of nitrobenzene into o and p-nitrophenol:
1. Method I: Nitrobenzene heated with solid KOH at 340 K gives a low yield of a mixture of O and P-nitrophenols.

2. Method II:

APPEARS IN
RELATED QUESTIONS
\[\ce{CH3CH2Br ->[aq NaOH][\Delta] A ->[KMnO4/H^+][\Delta] B ->[NH3][\Delta] C ->[Br2/NaOH] D}\] ‘D’ is:
Which of the following reaction is not correct.

‘A’ is:
Nitrobenzene on reaction with at 80-100°C forms which one of the following products?
What happens when oxidation of tert-butylamine with KMnO4?
Identify compounds A, B and C in the following sequence of reaction.
\[\ce{C6H5NO2 ->[Fe/HCl] A ->[HNO2][273 K] B ->[C6H5OH] C}\]
Identify A, B and C.

Account for the following.
Aniline does not undergo Friedel – Crafts reaction.
Account for the following.
Aniline does not undergo Friedel–Crafts reaction
Account for the following.
Aniline does not undergo Friedel – Crafts reaction.
