Answer:
See figure 1
Explanation:
On this case we have a <u>base</u> (methylamine) and an <u>acid</u> (2-methyl propanoic acid). When we have an acid and a base an <u>acid-base reaction </u>will take place, on this specific case we will produce an <u>ammonium carboxylate salt.</u>
Now the question is: <u>¿These compounds can react by a nucleophile acyl substitution reaction?</u> in other words <u>¿These compounds can produce an amide? </u>
Due to the nature of the compounds (base and acid), <u>the nucleophile</u> (methylamine) <u>doesn't have the ability to attack the carbon</u> of the carbonyl group due to his basicity. The methylamine will react with the acid-<u>producing a positive charge</u> on the nitrogen and with this charge, the methylamine <u>loses all his nucleophilicity.</u>
I hope it helps!
Answer:
Ionic or Electrovalent Bonding
Explanation:
There are primarily two categories of bonding between chemical entities. We have; Ionic Bonding and Covalent Bonding.
Ionic bonding or electrovalent bonding is the complete transfer of valence electron(s) between atoms. There is the transfer of electron from typically a metal to a non metal.
Covalent Bonding however involves the sharing of electrons between atoms. Depending on whuch atoms provide the electrons, it can be ordinary covalent oor coordinate covelent bond.
Answer:
Generally, a gas behaves more like an ideal gas at higher temperature and lower pressure, as the potential energy due to intermolecular forces becomes less significant compared with the particles' kinetic energy, and the size of the molecules becomes less significant compared to the empty space between them.
Explanation:
I am pretty sure it’s D.Sulfur
