Respuesta :
Any acid chloride residue on the product is cleaned off using a NaOH solution. The acyl chloride is converted by the NaOH into a salt that is extracted from the aqueous layer. To make sure that all of the acid is eliminated, the procedure is carried out twice.
How is N,N-diethyltoluamide Prepared?
Amides are typically made by reacting a derivative of a carboxylic acid with ammonia or a primary or secondary amine. Although acyl chlorides are the most practical for creating the most diverse range of amides, acid anhydrides or esters are occasionally utilized as the acid derivative. A good deal of the time, the rate of the reactions must be regulated by chilling or using a suitable solvent because of how quickly and exothermically the acyl chlorides react. It is important to employ at least a 100% excess of the nitrogen compound in the reaction, which creates HCl, which then reacts with one equivalent of amine (or ammonia) to create the amine salt.
To learn more about N,N-diethyltoluamide Visit: https://brainly.com/question/14408519
#SPJ4
