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प्रश्न
Write short notes on acetylation.
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उत्तर
The process of introducing an acetyl group \[\begin{array}{cc}
\phantom{.....}\ce{O}\\
\phantom{.....}||\\
\ce{(CH3 - C - )}
\end{array}\] into a molecule is called acetylation. The reaction occurs by nucleophilic substitution. There occurs a replacement of the hydrogen atom of −NH2 or > NH by the acetyl group.
Common acetylating agents used are acetyl chloride and acetic anhydride.
\[\begin{array}{cc}
\ce{O}\phantom{................}\ce{O}\phantom{..}\\
||\phantom{.................}||\phantom{..}\\
\ce{CH3CH2NH2 + CH3 - C - Cl -> \underset{N-Ethylacetamide}{CH3 - C - NH - CH2CH3} + HCl}
\end{array}\]
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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.
What is the action of acetic anhydride on diethylamine?
What is the action of the following reagents on aniline?
Acetic anhydride
What is the action of the following reagents on aniline?
Hot and conc. sulphuric acid
What is the role of \[\ce{HNO3}\] in the nitrating mixture used for nitration of benzene?
When bromination of aniline is carried out by protecting – NH2. The major product is
Give reasons for the following observation:
Aniline is acetylated before nitration reaction.
Give reasons for the following observation:
Aniline does not react with methyl chloride in the presence of anhydrous AlCl3 catalyst.
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.
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:
\[\ce{CH3 - CH2 - CH2 - I ->[NaCN] A ->[OH-][Partial hydrolysis] B ->[NaOH][Br2] \underset{(major)}{C}}\]
