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Acetanilide is prepared by the reaction ...

Acetanilide is prepared by the reaction of acetyl chloride on

A

acetamide

B

aniline

C

acetaldehyde

D

benzene

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The correct Answer is:
To prepare acetanilide, we need to react acetyl chloride with an appropriate compound. Let's break down the steps to find the correct compound. ### Step-by-Step Solution: 1. **Identify Acetanilide Structure**: Acetanilide is a compound that consists of a benzene ring with an amide functional group. Its structure can be represented as: \[ \text{C}_6\text{H}_5\text{NHCOCH}_3 \] This indicates that it contains a phenyl group (from benzene) and an acetamide group. 2. **Identify Acetyl Chloride**: Acetyl chloride is represented as: \[ \text{CH}_3\text{C(=O)Cl} \] This compound is a reactive acyl chloride that can react with nucleophiles. 3. **Determine the Reactant**: To form acetanilide, we need a compound that contains a nucleophilic amine group. The most suitable candidate is **aniline**, which has the structure: \[ \text{C}_6\text{H}_5\text{NH}_2 \] Aniline contains an amino group (-NH2) that can act as a nucleophile. 4. **Reaction Mechanism**: When aniline reacts with acetyl chloride, the nucleophilic nitrogen of the aniline attacks the carbonyl carbon of the acetyl chloride. This results in the formation of acetanilide and hydrochloric acid (HCl) as a byproduct: \[ \text{C}_6\text{H}_5\text{NH}_2 + \text{CH}_3\text{C(=O)Cl} \rightarrow \text{C}_6\text{H}_5\text{NHCOCH}_3 + \text{HCl} \] 5. **Conclusion**: Therefore, acetanilide is prepared by the reaction of acetyl chloride with **aniline**. ### Final Answer: Acetanilide is prepared by the reaction of acetyl chloride on **aniline**. ---

To prepare acetanilide, we need to react acetyl chloride with an appropriate compound. Let's break down the steps to find the correct compound. ### Step-by-Step Solution: 1. **Identify Acetanilide Structure**: Acetanilide is a compound that consists of a benzene ring with an amide functional group. Its structure can be represented as: \[ \text{C}_6\text{H}_5\text{NHCOCH}_3 ...
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ICSE-ORGANIC COMPOUNDS CONTAINING NITROGEN-EXERCISE (PART-I OBJECTIVE QUESTIONS)
  1. Conversion of nitrobenzene to aniline is carried out in

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  2. Towards electrophilic substitution, the most reactive will be

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  3. Acetanilide is prepared by the reaction of acetyl chloride on

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  4. Which of the following gives carbylamine reaction?

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  5. The compound obtained by heating a mixture of a primary amine and chlo...

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  6. which of the following reactions will not give a primary amine ?

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  7. Gabrial synthesis is used for the preparation of

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  8. Nitrosoamines (R2 N-N=O) are insoluble in water. On heating them with ...

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  9. Which of the following is a 3^@ amine?

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  10. The correct IUPAC name for CH2=CHCH2NHCH3 is

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  11. Amongst the following, the strongest base in aqueous medium is .

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  12. Which of the following is the weakest Bronsted base?

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  13. Benzyl amine may be alkylated as shown in the following equation : ...

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  14. Which of the following reagents would not be a good choice for reducin...

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  15. In order to prepare a 1^(@) amine from an alkyl halide with simultaneo...

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  16. The souce of nitrogen in Gabriel synthesis of amines is

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  17. Amongst the given set of reactants the most appropriate for preparing ...

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  18. The best reagent for converting 2-phenylpropanamide into 2-phenylpropa...

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  19. The best reagent for converting, 2-phenylpropanamide into 1-phenyletha...

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  20. Hofmann bromide degradation reaction is shown by

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