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: 0.25 mol
Explanation:
Use the formula n=N/NA
n= number of mols
N = number of particles
Nᵃ = Avogadros constant = 6.02 x
So, n=
The 10 to the power of 23 cancels out and you are left with 1.505/6.02, which is approximately 1/4. This is the same as 0.25 mol.
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Answer: The molar mass of H2S is greater than the molar mass of NH3, making the velocity and effusion rate of NH3 particles faster.
Effusion rate is inversely proportional to molar mass.
NH3 will have a higher average molecule velocity, so it will diffuse faster and will reach the other side of the room more quickly.
Explanation: change up your response a bit