Answer :
After the addition of the aldehyde, any remaining Grignard reagent in the reaction mixture will react with water or any other protic solvent present, resulting in the formation of the corresponding alkane and a magnesium hydroxide salt.
Grignard reagents are highly reactive organometallic compounds that are commonly used in organic synthesis to form new carbon-carbon bonds. They are prepared by reacting an organic halide with magnesium metal in anhydrous ether.
Grignard reagents are strong nucleophiles and can react with a wide range of electrophiles, including aldehydes, ketones, esters, and acid chlorides.
When a Grignard reagent is added to an aldehyde, it acts as a nucleophile and attacks the electrophilic carbonyl carbon of the aldehyde.
This results in the formation of an alcohol intermediate, which can then undergo further reaction to form a variety of products depending on the conditions of the reaction.
However, it is important to note that any remaining Grignard reagent in the reaction mixture can react with water or any other protic solvent present, resulting in the formation of the corresponding alkane and a magnesium hydroxide salt.
This is known as a "quenching" reaction and is used to terminate the reaction and prevent further reaction with other electrophiles.
To learn more about nucleophiles, refer below:
https://brainly.com/question/30713995
#SPJ11
