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The chemical reaction is:
C6H5NH2 + (CH3CO)2O → C6H5NHCOCH3 + CH3COOH

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Why add of little amount from acetic anhydride in synthesis of acetanilide?

Adding a small amount of acetic anhydride helps to facilitate the acetylation reaction with aniline, leading to the formation of acetanilide. The acetic anhydride serves as an acetylating agent that transfers an acetyl group to the amine group of aniline, resulting in the desired product. The use of an excess of acetic anhydride is avoided to prevent side reactions and to optimize the yield of acetanilide.


Reaction of methyl amine and acetic anhydride?

The reaction between methylamine and acetic anhydride results in the formation of N-methylacetamide as the primary product. In this reaction, acetic anhydride reacts with methylamine to form an amide functional group. This reaction is a common method for the synthesis of amides in organic chemistry.


What is the balanced equation for the reaction between salicylic acid and acetic anhydride?

The balanced equation for the reaction between salicylic acid and acetic anhydride to form aspirin (acetylsalicylic acid) is: salicylic acid + acetic anhydride → aspirin + acetic acid.


What is the mechanism of the salicylic acid and acetic anhydride reaction?

The reaction between salicylic acid and acetic anhydride involves the substitution of a hydroxyl group in salicylic acid with an acetyl group from acetic anhydride. This reaction is catalyzed by an acid, typically sulfuric acid, and results in the formation of aspirin and acetic acid as byproducts.


What would happen if the excess acetic anhydride is not removed in the reaction vessel?

If excess acetic anhydride is not removed from the reaction vessel, it can lead to side reactions or undesired byproducts in the final product. It could also affect the purity of the desired compound and make purification more challenging. Additionally, it can pose safety hazards as acetic anhydride is a corrosive and hazardous chemical.

Related Questions

What is the alternative route of synthesis of acetanilide?

Acetanilide can also be synthesized by reacting aniline with acetic anhydride, instead of acetyl chloride. This is known as the Acetic Anhydride Method.


Why add of little amount from acetic anhydride in synthesis of acetanilide?

Adding a small amount of acetic anhydride helps to facilitate the acetylation reaction with aniline, leading to the formation of acetanilide. The acetic anhydride serves as an acetylating agent that transfers an acetyl group to the amine group of aniline, resulting in the desired product. The use of an excess of acetic anhydride is avoided to prevent side reactions and to optimize the yield of acetanilide.


What is the reaction when zinc acetic anhydride and glacial acetic acid are combine?

When zinc is reacted with acetic anhydride and glacial acetic acid, a complex called zinc acetate is formed. The reaction typically involves the displacement of acetic anhydride by acetic acid to form zinc acetate. The overall reaction is a redox reaction where zinc is oxidized and acetic anhydride is reduced.


Reaction of methyl amine and acetic anhydride?

The reaction between methylamine and acetic anhydride results in the formation of N-methylacetamide as the primary product. In this reaction, acetic anhydride reacts with methylamine to form an amide functional group. This reaction is a common method for the synthesis of amides in organic chemistry.


In the aspirin synthesis excess acetic anhydride is hydrolyzed by the addition of water which converts the anhydride into acetic acid Write the balanced equation for this reaction?

The reaction is: (CH3CO)2O + H2O = 2 CH3COOH


What reagents may be used for the preparation of acetanilide?

Acetanilide can be prepared using aniline and acetic anhydride as reagents. The reaction typically requires the presence of a catalyst, such as zinc chloride, to facilitate the acetylation of aniline to form acetanilide. The reaction is usually carried out in the presence of a base, like sodium acetate, to neutralize the acidic byproduct formed during the reaction.


What is the balanced equation for the reaction between salicylic acid and acetic anhydride?

The balanced equation for the reaction between salicylic acid and acetic anhydride to form aspirin (acetylsalicylic acid) is: salicylic acid + acetic anhydride → aspirin + acetic acid.


What is an alternative reagent to ethanoic anhydride in the synthesis of aspirin from salicylic acid?

Synthesis of acetyl chloride via the reaction of acetic acid with sulphuric acid


What is the mechanism of the salicylic acid and acetic anhydride reaction?

The reaction between salicylic acid and acetic anhydride involves the substitution of a hydroxyl group in salicylic acid with an acetyl group from acetic anhydride. This reaction is catalyzed by an acid, typically sulfuric acid, and results in the formation of aspirin and acetic acid as byproducts.


What would happen if the excess acetic anhydride is not removed in the reaction vessel?

If excess acetic anhydride is not removed from the reaction vessel, it can lead to side reactions or undesired byproducts in the final product. It could also affect the purity of the desired compound and make purification more challenging. Additionally, it can pose safety hazards as acetic anhydride is a corrosive and hazardous chemical.


Chemical reaction of hydrolysis of acetic anhydride?

Acetic anhydride undergoes hydrolysis in the presence of water to form acetic acid and a byproduct, typically a carboxylic acid or alcohol. The reaction is a typical nucleophilic acyl substitution reaction, where water acts as a nucleophile attacking the acetic anhydride to break the anhydride bond and form acetic acid.


Is aspirin synthesis an esterification reaction?

No, aspirin synthesis is not an esterification reaction. It involves the reaction of salicylic acid with acetic anhydride to form acetylsalicylic acid (aspirin) and acetic acid through an acetylation reaction. Esterification typically involves the reaction of an alcohol with a carboxylic acid to form an ester.