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Assertion: Benzenediazonium ion couples with aniline effectively in a weakly acidic medium.

Reason: In a weakly acidic medium, aniline becomes respectively more activated for electrophilic substitution.

 

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Important Questions on Amines

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Directions: Each of these questions contain an assertion followed by reason. Read them carefully and answer the question on the basis of the following options. You have to select the one that best describes the two statements.
Assertion: Aniline reacts with concentrated H2SO4 to form anilinium sulphate, which on heating to about 473K forms mainly p-aminobenzene suiphonic acid (suiphanilic acid).
Reason: Sulphanilic acid exists as a dipolar ion.
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Directions: Each of these questions contain an assertion followed by reason. Read them carefully and answer the question on the basis of the following options. You have to select the one that best describes the two statements.

Assertion: In order to convert R-Cl to pure R-NH2, Gabriel phthalimide synthesis can be used.
Reason: With proper choice of alkyl halides, phthalimide synthesis can be used to prepare 1°,2° or 3° amines.

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In Sandmeyer's reaction the salt involved is:-
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In the reaction the compound (A) is known as:-

C6H5CHO+C6H5NH2C6H5N=CHC6H5A+H2O 

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What is the product formed when nitrobenzene reacts with zinc dust and aqueous ammonium chloride?
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The compound which gives an oily nitrosamine on reaction with nitrous acid at low temperature :-
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Ph-NH20°CHNO2ABF3HFBC, C is:-
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Best method to form aromatic iodide is: -