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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.

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What is the equation for the hydrolysis of C4H9Br with NaOH?

The hydrolysis reaction of C4H9Br with NaOH can be represented as follows: C4H9Br + NaOH -> C4H9OH + NaBr This reaction involves the substitution of the bromine atom in C4H9Br with the hydroxide ion from NaOH, resulting in the formation of C4H9OH (butanol) and NaBr (sodium bromide).


How do you convert aniline to benzamide?

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.


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.


Which equation has water as a product in the chemical reaction-?

bromine water? The reaction between hexene, bromine, and water is an addition reaction.


What is the important of NaOH in preparation of bromoaniline?

NaOH is important in the preparation of bromoaniline as it is used to deprotonate the aniline molecule, making it more nucleophilic. This allows the bromine atom to substitute for one hydrogen atom on the benzene ring to form bromoaniline. Additionally, NaOH helps to maintain the reaction conditions at a suitable pH for the substitution reaction to occur efficiently.

Related Questions

What is the equation for the hydrolysis of C4H9Br with NaOH?

The hydrolysis reaction of C4H9Br with NaOH can be represented as follows: C4H9Br + NaOH -> C4H9OH + NaBr This reaction involves the substitution of the bromine atom in C4H9Br with the hydroxide ion from NaOH, resulting in the formation of C4H9OH (butanol) and NaBr (sodium bromide).


How do you convert aniline to benzamide?

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.


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.


Which equation has water as a product in the chemical reaction-?

bromine water? The reaction between hexene, bromine, and water is an addition reaction.


What is the important of NaOH in preparation of bromoaniline?

NaOH is important in the preparation of bromoaniline as it is used to deprotonate the aniline molecule, making it more nucleophilic. This allows the bromine atom to substitute for one hydrogen atom on the benzene ring to form bromoaniline. Additionally, NaOH helps to maintain the reaction conditions at a suitable pH for the substitution reaction to occur efficiently.


What is the dissociation reaction of NaOH to H2O?

The dissociation reaction of NaOH in water is as follows: NaOH (s) → Na+ (aq) + OH- (aq)


What is the equation for formation of benzamide from benzoic acid and ammonia?

The reaction between benzoic acid and ammonia to form benzamide is represented by the following equation: C6H5COOH + NH3 -> C6H5CONH2 + H2O


What type of reaction is it when methane reacts with bromine?

The reaction between methane and bromine is a substitution reaction, specifically a halogenation reaction. In this reaction, one or more hydrogen atoms in methane are replaced by bromine atoms to form bromomethane.


How do you remove bromine in Bromobenzene?

To remove bromine in bromobenzene, you can use a reducing agent such as zinc or tin with hydrochloric acid. The reducing agent will react with the bromine, converting it into a bromide ion which can then be easily separated from the organic compound. This process is known as reductive debromination and is commonly used in organic chemistry to remove halogens from aromatic compounds.


Which reaction represents an unbalanced neutralization reaction?

HCl + NaOH -> NaCl + H2O is an unbalanced neutralization reaction.


What forms from the reaction of bromine with acetophenone?

The reaction of bromine with acetophenone can yield several products, depending on reaction conditions. One common product is α-brominated acetophenone, where bromine adds to the alpha carbon of the carbonyl group. This reaction can also lead to dibrominated acetophenone if excess bromine is used.


What reaction of bromine and sodium chloride?

no reaction