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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

What is the role of HNOX3 in the nitrating mixture used for nitration of benzene?

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प्रश्न

What is the role of \[\ce{HNO3}\] in the nitrating mixture used for nitration of benzene?

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उत्तर

\[\ce{HNO3}\] acts as a base in the nitrating mixture \[\ce{(HNO3 + H2SO4)}\] and provides the electrophile.

\[\ce{HNO3 + H2SO4 -> \underset{Electrophile}{NO^{+}2 + HSO^{-}4} + H2O}\]

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अध्याय 13: Amines - Multiple Choice Questions (Type - I) [पृष्ठ १८८]

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एनसीईआरटी एक्झांप्लर Chemistry Exemplar [English] Class 12
अध्याय 13 Amines
Multiple Choice Questions (Type - I) | Q 38 | पृष्ठ १८८

संबंधित प्रश्न

How is chlorobenzene prepared from aniline?


What is the action of the following reagents on aniline?

Bromine water


Give reasons for the following:

Aniline does not undergo Friedel- Crafts reaction.


Write the structures of main products when aniline reacts with the following reagents :

Br2 water


Write the chemical equations involved when aniline is treated with the following reagents:

Br2 water


Account for the following:

Although the amino group is o, p-directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of m-nitroaniline.


Write short notes on acetylation.


Illustrate the following reactions giving suitable example in each case 

Acetylation of amines


How will you convert the following?

Aniline into N−phenylethanamide


Assertion: N, N-Diethylbenzene sulphonamide is insoluble in alkali.

Reason: Sulphonyl group attached to nitrogen atom is strong electron-withdrawing group.


How can the activating effect of the −NH2 group in aniline be controlled?


Assertion (A): Bromination of benzoic acid, gives m-bromobenzoic acid.

Reason (R): Carboxyl group increases the electron density at the meta position.


Aniline does not give Friedel-Crafts reaction. Give a reason.


Given below are two statements:

Statement I: Aniline does not undergo a Friedel-Crafts alkylation reaction.

Statement II: Aniline cannot be prepared through Gabriel synthesis.

In the light of the above statements, choose the correct answer from the options given below:


Identify the major product C formed in the following reaction sequence:

\[\ce{CH3 - CH2 - CH2 - I ->[NaCN] A ->[OH-][Partial hydrolysis] B ->[NaOH][Br2] \underset{(major)}{C}}\]


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