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प्रश्न
Why is benzene diazonium chloride not stored and is used immediately after its preparation?
उत्तर
The reaction of aniline with nitrous acid at 273 - 278 K produces benzene diazonium chloride. The reaction of sodium nitrite with hydrochloric acid produces nitrous acid in the reaction mixture. Diazotisation is the process of converting primary aromatic amines into diazonium salts. Because of its instability, the diazonium salt is generally not used immediately after preparation.
The crystalline solid benzene diazonium chloride is colorless.
It is easily soluble in water and stable at room temperature but it reacts with water when warmed.
In the dry state, it decomposes easily.
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संबंधित प्रश्न
Write equations of the following reactions:
Acetylation of aniline
Arenium ion involved in the bromination of aniline is:
(i)
(ii)
(iii)
(iv)
How will you carry out the following conversions?
toluene `->` p-toluidine
Which of the following statement about primary amines is false?
Aniline when treated with cone. HNO3 gives
Which of the following is true characteristic feature of aniline?
Which of the following is the most stable diazonium salt?
Consider the following compounds:
(i) p-methyl aniline
(ii) N, N-dimethylaniline
(iii) N-ethyl aniline
(iv) N-ethyl-N-methyl aniline
The compounds which do not form diazonium salt with ice-colds NaNO2 and HCl are:
Identify A and B for the following reaction:
What are polymers?
How will the following be converted? (Give chemical equation)
Aniline to benzene diazonium chloride.
