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The nitrosation of N,N-dimethylaniline takes place through the attack of electrophile:

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Important Questions on Amines

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EMBIBE CHAPTER WISE PREVIOUS YEAR PAPERS FOR CHEMISTRY>Chapter 23 - Amines>KEAM 2020>Q 1
Which one of the following can be prepared by Gabriel phthalimide synthesis?
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EMBIBE CHAPTER WISE PREVIOUS YEAR PAPERS FOR CHEMISTRY>Chapter 23 - Amines>KEAM 2019>Q 2
Arylbromides are not good candidates for
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EMBIBE CHAPTER WISE PREVIOUS YEAR PAPERS FOR CHEMISTRY>Chapter 23 - Amines>KEAM 2019>Q 3
In the Hofmann rearrangement of primary amides having optically active group with S-configuration, the product amine has
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EMBIBE CHAPTER WISE PREVIOUS YEAR PAPERS FOR CHEMISTRY>Chapter 23 - Amines>KEAM 2019>Q 4
The strongest base among the following is
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EMBIBE CHAPTER WISE PREVIOUS YEAR PAPERS FOR CHEMISTRY>Chapter 23 - Amines>KEAM 2020>Q 5
The reagent that is used to distinguish between a secondary amine and a tertiary amine is;
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EMBIBE CHAPTER WISE PREVIOUS YEAR PAPERS FOR CHEMISTRY>Chapter 23 - Amines>KEAM 2019>Q 6

The product formed in the below reaction is

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EMBIBE CHAPTER WISE PREVIOUS YEAR PAPERS FOR CHEMISTRY>Chapter 23 - Amines>KEAM 2019>Q 7

Cyclohexylamine and aniline can be distinguished.

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EMBIBE CHAPTER WISE PREVIOUS YEAR PAPERS FOR CHEMISTRY>Chapter 23 - Amines>KEAM 2018>Q 8
The nitrosation of N,N-dimethylaniline takes place through the attack of electrophile: