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JulsSmile [24]
2 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]2 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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Answer:

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Explanation:

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2 years ago
Suppose that the microwave radiation has a wavelength of 12.4 cm . How many photons are required to heat 255 mL of coffee from 2
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Answer:

Explanation:

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= 39438.3 J  .

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5 0
2 years ago
A tank holds 6.90 m3 of water. What is the volume in ft3? (3.28 ft = 1 m, Remember significant figures, but this answer does not
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Volume of tank = 6.9 m^{3} (given)

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Since, the minimum number of decimal places in the above multiplication operation is 1 so, the final result must be upto 1 decimal place only.

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Answer:

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