Simply allow to react benzyl bromide with aqueous NaOH in hot condition.
Chat with our AI personalities
Benzyl bromide can be converted to benzyl alcohol through a nucleophilic substitution reaction using a strong nucleophile such as sodium hydroxide (NaOH). The reaction involves the attack of the hydroxide ion on the bromine atom of benzyl bromide, resulting in the displacement of bromine and formation of benzyl alcohol. The mechanism typically occurs in a polar solvent like water or alcohol.
Methyl bromide cannot be directly converted into ethyl bromide. However, methyl bromide can be converted into ethyl bromide through a substitution reaction by reacting it with ethyl alcohol in the presence of a strong base, such as sodium hydroxide, to form ethyl bromide.
The ester formed from benzyl alcohol and acetic acid is benzyl acetate.
Yes, benzyl alcohol is flammable. It has a flash point of 145°F and can ignite if exposed to an open flame, spark, or heat source. It is important to handle benzyl alcohol with caution and store it away from sources of ignition.
The pKa value of benzyl alcohol is around 15.4. This means that benzyl alcohol is a weak acid and tends to lose a proton in solution.
No, benzyl salicylate is not a base. It is an ester formed by the condensation of salicylic acid with benzyl alcohol.