n‑methyl‑2‑pyrrolidone is an aprotic solvent used in many industrial processes. draw the structure of the product formed when it
1 answer:
The structure of n‑methyl‑2‑pyrrolidone when it is heated with aqueous acid. product is given below
<h3 /><h3>What is aprotic solvent?</h3>A polar solvent without an acidic proton is known as a polar aprotic solvent. These solvents don't include hydroxyl or amine groups. These solvents can act as proton acceptors, but unlike protic solvents, they do not act as proton donors in hydrogen bonding.
After being exposed to a strong aqueous acidic media and being heated, N-methyl-2-pyrrolidone opens up, forming a molecule with a carboxylic group at one end and a protonated nitrogen atom with a methyl group connected to it at the other.
Alcohol, water, hydrogen fluoride, formic acid, acetic acid, ammonia, methanol, ethanol, and other well-known substances are a few examples of polar protic solvents. Polar aprotic solvents, on the other hand, lack acidic protons and do not function as donors during hydrogen bonding.
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Answer:
a) find attached image 1
b) find attached image 2
Explanation :
The more stable radical is formed by a reaction with smaller bond dissociation energy.
since the bond dissociation for cleavage of the bond to form primary free radical is higher, more energy must be added to form it. This makes primary free radical higher in energy and therefore less stable than secondary free radical.
