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Which of the following amines will form ...

Which of the following amines will form stable doazonium salt at `273-283K`?

A

Ethylamine

B

Aniline

C

Dimethylamine

D

Benzylamine

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The correct Answer is:
To determine which of the following amines will form a stable diazonium salt at 273-283 K, we need to analyze the structure and stability of the diazonium salts formed from each amine. The amines given are ethylamine, aniline, dimethylamine, and benzylamine. ### Step-by-Step Solution: 1. **Understanding Diazonium Salts**: Diazonium salts are formed when primary amines react with nitrous acid (HNO2) at low temperatures. The general formula for a diazonium salt is R-N2^+X^-, where R is an alkyl or aryl group and X is a halide or another anion. 2. **Analyzing Each Amine**: - **Ethylamine (C2H5NH2)**: This is a primary aliphatic amine. When ethylamine forms a diazonium salt, the positive charge on the nitrogen does not have resonance stabilization from a benzene ring. Therefore, the diazonium salt formed from ethylamine is not stable at low temperatures. - **Aniline (C6H5NH2)**: Aniline is a primary aromatic amine. When aniline forms a diazonium salt, the positive charge on the nitrogen can be delocalized into the benzene ring through resonance. This delocalization stabilizes the diazonium salt, making it stable at low temperatures (273-283 K). - **Dimethylamine (C2H7N)**: This is a secondary amine. Similar to ethylamine, dimethylamine does not have the resonance stabilization that aniline has. Therefore, the diazonium salt formed from dimethylamine is also not stable at low temperatures. - **Benzylamine (C6H5CH2NH2)**: Benzylamine is a primary amine with a benzyl group. The diazonium salt formed from benzylamine does not have the same level of resonance stabilization as aniline because the positive charge cannot be delocalized into the benzene ring. Thus, it is less stable than aniline's diazonium salt. 3. **Conclusion**: Among the given amines, only **aniline** can form a stable diazonium salt at 273-283 K due to the resonance stabilization provided by the benzene ring. ### Final Answer: **Aniline** will form a stable diazonium salt at 273-283 K.
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AAKASH INSTITUTE ENGLISH-AMINES -Assignment Section -A Competition Level Questions
  1. The action of nitrous acid on an aliphatic primary amine gives

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  2. The gas evolved when methylamine reacts with nitrous acid is….

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  3. Which of the following amines will form stable doazonium salt at 273-2...

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  4. A mixture of 1^(@), 2^(@) and 3^(@) amines can be separated by Hinsber...

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  5. Explain the following: Aniline readily reacts with bromine to give ...

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  6. CH3CH2Cloverset(NaCN)to Xoverset(Ni//H2)to Yunderset("anhydride")overs...

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  7. Identify X in the series

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  8. A compound 'A' when treated with HNO(3) (in presence of H(2)SO(4)) giv...

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  9. A secondary amine is a compound which possesses .

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  10. A compound (X) has the molecular formula C7 H7O . On treatment with ...

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  11. What is the end product in the following sequence of reactions? C(2)...

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  12. Reaction of ammonia with excess Cl2 gives

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  13. Amines are highly soluble in

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  14. Amides can be converted into amines by a reaction named after

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  15. 2,4,6-tibromo aniline is a product of

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  16. Benzenediazonium chloride on reaction with water gives

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  17. Benzene diazonium chloride on reaction with phenol in a basic medium g...

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  18. When benzenediazonium chloride is heated with fluoro boric acid, fluor...

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  19. Benzenediazonium chloride is reduced to benzene by

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  20. Diazotisation can be carried out by the action of NaNO(2) and dilute H...

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