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प्रश्न
Write the reaction of aromatic primary amine with nitrous acid.
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उत्तर
Aromatic amine react with nitrous acid (prepared in situ from NaNO2 and a mineral acid such as HCl) at 273 − 278 K to form stable aromatic diazonium salts, i.e., NaCl and H2O.
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संबंधित प्रश्न
How are propan-1-amine and propan-2-amine prepared from oxime?
Write a short note on Hoffmann bromamide degradation.
Give the structures of A, B and C in the following reactions :
Give the structures of A, B and C in the following reaction:
\[\ce{CH3COOH ->[NH3][\Delta] A ->[NaOBr] B ->[NaNO2/HCl] C}\]
Mention 'two' uses of propan-2-one.
Give the structures of A, B and C in the following reactions :
Write structures of compounds A and B in each of the following reactions:
Which nitrogen containing compound amongst the following would undergo Mendius reduction to furnish primary amine \[\ce{(R - NH2)}\]?
What is the product when \[\ce{C6H5CH2NH2}\] reacts with \[\ce{HNO2}\]?
What is the best reagent to convert nitrile to primary amine?
Identify A and B in the following reaction.
Write following conversions:
nitrobenzene `->` acetanilide
Describe Gabriel's phthalimide synthesis. (Give reaction)
The compound X is which of the following?
\[\ce{CH3CN ->[Na + C2H5OH] x}\]
When primary amines are treated with HCl, the product obtained is which of the following?
Which of the following CANNOT be prepared by ammonolysis of alkyl halide?
Give reasons for the following:
Ammonolysis of alkyl halides is not a good method to prepare pure primary amines.
Which of the following reaction DOES NOT involve Hoffmann bromamide degradation?
Which of the following amines can be prepared by Gabriel phthalimide reaction?
Write a short note on the following:
Ammonolysis
