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Using Grabriel phthallmide synthesis aro...

Using Grabriel phthallmide synthesis aromatic primary amines cannot be prepared. Do you agree with this statement? Justify.

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BODY BOOKS PUBLICATION-AMINES-EXAMPLE
  1. Arrange the following in increasing order of basic strength: C2H5NH2...

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  2. Amines are basic. Arrange the following amines in the increasing order...

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  3. Using Grabriel phthallmide synthesis aromatic primary amines cannot be...

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  4. Illustrate coupling reaction with example.

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  5. Alcoholic AgCN, CH3CI, alc.KCN and LiAlH4 are good friends.One day CH3...

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  6. Alcoholic AgCN, CH3CI, alc. KCN and LiAlH4are good friends. One day CH...

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  7. Identify the main product and name the reactions.When ethylamine treat...

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  8. Identify the main product and name the reactions.When amide treated wi...

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  9. How will you bring about the following conversions :- Benzene diazoniu...

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  10. Convert benzene diazonium chloride to p-amino azobenzene.

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  11. Complete the following reaction and name it.C6H5N2^+Cl^- overset (CuCl...

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  12. Complete the following reaction and name it. CH3COOH+CH3OH overset (H...

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  13. Complete the following reaction and name it. C2H5 -NH2 +CHCl3 overset ...

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  14. Name the product A.

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  15. Starting from benzene diazonium chloride prepare:Benzene

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  16. Starting from benzene diazonium chloride prepare:Iodobenzine

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  17. Starting from benzene diazonium chloride prepare:Flurobenzene

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  18. (CH3)3Nboils at lower temperature than the corresponding primary amine...

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  19. If you treat aniline with fuming H2SO4 at 475K it gives a compound whi...

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  20. If you treat aniline with fuming H2SO4 at 475K it gives a compound whi...

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