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Pure amines cannot be prepared by ammono...

Pure amines cannot be prepared by ammonolysis. Why ?

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The ammonolysis of alkyl halides give a mixture of amines. Ammonia with lone pair of electrons attack the alkyl halide, gives `1^@` - amines. As `1^@` - amines have a line pair of electrons, it attacks again an alkyl halide molecule and gives `2^@`-amines. This reaction will go on until the quaternary ammonium salts are formed.
Now, to separate this mixture of amines is a hard task. Hence pure amines cannot be prepared. The ammonolysis of alkyl halides can be shown below.
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OMEGA PUBLICATION-AMINES-MULTIPLE CHOICE QUESTIONS
  1. Pure amines cannot be prepared by ammonolysis. Why ?

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  2. Stephen reduction· converts cyanides to

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  3. Classify the following as pure substances or mixtures:

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  4. Identify the following as homogenous and hetrogenous mixture :

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  5. Which of the following is not an ambident nucleophile?

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  6. Which of the following substances on treatment with P2O5 gives ethanen...

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  7. Methyl cyanide on treatment with methyl magnesium bromide followed by...

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  8. Which of the following represents the poisonous gas which caused trage...

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  9. When propane is subjected fo the treatment with fuming nitric acid at ...

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  10. Which of the following is not a nitro derivative?

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  11. Which of the following structures represent nitrolic acid?

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  12. Which reagent should be employed to get ethyl carbylamine from ethyl i...

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  13. NO2^+ is called

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  14. Explain Mendius reaction.

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  15. Aniline upon heating with conc.HNO3 and conc.H2SO4 mixture gives:

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  16. Which are given by carbylamine reaction?

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  17. Nitrobenzene is subjected to reductfon with zinc dust and ammonium chl...

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  18. A primary nitroalkane is treated with nitrous acid, which of the follo...

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  19. Nitromethane is subjected to the treatment with chlorine in the presen...

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  20. The electrolytic reduction of nitrobenzene in strongly acidic medium p...

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  21. Which of the following on boiling with Na2CO3(aq) gives aniline?

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