Answer:
Time is relative - and science is still arguing about singlet versus doublet Carbenes; they fought over whether Oxygen was “real”, and refused to believe in Radium until one by one they SAW that drop glow! (And affect photographic film).
Explatnation:
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!
Na = 23 x 2.40 = 55.2
O = 16 x 2.40 = 38.4
H = 1 x 2.40 = 2.40
55.2 + 38.4 + 2.4 = 96
2.40 mol of NaOH = 96 amu
The answer is C ionic bonds