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Aniline can be converted to benzamide by reacting it with benzoyl chloride in the presence of a base, such as pyridine, at room temperature. This reaction forms a carbamate intermediate which then undergoes hydrolysis to produce benzamide.

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1y ago

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How do you convert toluene to aniline?

To convert toluene to aniline, you can first nitrify toluene to form nitrotoluene using a mixture of concentrated nitric and sulfuric acids. Then, the nitrotoluene can be reduced to aniline through catalytic hydrogenation or using reducing agents like iron and hydrochloric acid or lithium aluminum hydride. This process involves the substitution of the nitro group with an amino group, resulting in the formation of aniline.


What is the odour of benzamide?

irritating odour and irritates the eyes...


Is benzamide acidic?

No; the derivate benzoic acid is of course acidic.


How to convert aniline to picric acid?

React aniline with HCl/NaNO2 (diazotisation) followed by reaction with KOH to give phenol. Nitration of phenol with fuming nitric acid gives picric acid (or trinitrophenol).


Is Benzamide a solid liquid or gas in room temperature?

It is a white solid at room temperature: 24-22 celcius


What is formed when you react benzamide with hydrochloric acid and sodium hydroxide?

When benzamide is reacted with hydrochloric acid, benzamidium chloride is formed. When benzamidium chloride is then treated with sodium hydroxide, benzamide regenerates. This reaction is a reversible acid-base reaction.


What is the difference between Aniline Point and Mixed Aniline Point?

There is no any such difference between Aniline point and mixed Aniline point . . . . .


What does benzamide look like?

Benzamideis an off-white solid


What is the chemical formula of aniline hydrochloride?

The formula of aniline is C6H7N and the formula of ethanol is C2H5OH.


How do you convert aniline into phenyl hydrazine?

Aniline can be converted into phenyl hydrazine by reacting it with hydrazine hydrate in the presence of an acid catalyst such as hydrochloric acid. The reaction proceeds through the formation of a diazonium salt intermediate, which then reacts with excess hydrazine to form phenyl hydrazine.


What is a benzamide?

A benzamide is a compound that consists of a benzene ring with an amide functional group attached. It is commonly used in organic synthesis and pharmaceuticals due to its biological activity. Benzamides are found in drugs used to treat various conditions such as nausea, Parkinson's disease, and certain cancers.


Reaction of benzamide with bromine and NaOH?

Benzene is a very stable compound due to its ring structure and pi bonds. Composed only of carbon and hydrogen, it has no groups for NaOH (or other strong bases or strong acids for that matter) to react with.