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The 2,4 and 5 positions are accessible for nitration of 1,3‑dimethylbenzene. The final product is shown in the image attached.
<h3>What is nitration?</h3>Nitration is a type of reaction in which the nitro group (-NO2) is introduced to an aromatic ring. We have to note that in the compound 1,3‑dimethylbenzene, the 2,4 and 5 positions are accessible for nitration as shown.
Hence, the nitration of 1,3‑dimethylbenzene occurs as shown in the image attached with the compound shown being the major product.
Learn more about nitration: brainly.com/question/5346392
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>
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