Question

Imine formation from an aldehyde and an amine proceeds reversibly under slightly acidic conditions. The reaction is reversible due to acid-catalyzed hydrolysis of the imine. Imine formation generates an equivalent of water. Given these facts, explain why the imine can be isolated from the reaction mixture.

Answer 1

Answer:

Imine can be isolated from the reaction mixture as water is continuously removed from the reaction chamber

Explanation:

In this reaction, a non -aqueous solvent  is not used (not mentioned in the question). Thus, we can say that there is continuous removal water under suitable reacting conditions and hence the imine formed is left behind.