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JulsSmile [24]
3 years ago
9

Draw a mechanism for the reaction of methylamine with 2-methylpropanoic acid. Draw any necessary curved arrows. Show the product

s of the reaction. Include any nonzero formal charges and all lone pairs of electrons. Indicate which side of the reaction is favored at equilibrium.

Chemistry
1 answer:
Nitella [24]3 years ago
5 0

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!

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