Organic Chemistry
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Provide the product formed from the reaction shown below.
Describe how the given reaction leads to the desired product.
For the electrophilic aromatic substitution of the given diazonium ion and the nucleophile, show the correct mechanism of the nucleophilic attack on the diazonium ion.
Write a reasonable mechanism for the following reaction.
Draw the structure of the major product expected from the reaction of naphthalen-1-amine with sodium nitrite in dilute hydrochloric acid.
Show how you would make each of the compounds shown below using 2-methylaniline as your starting material.
Predict the identity of products of the reaction shown below.
Propose the synthesis of the following molecule when the starting compound is 2,3-dimethylaniline.
Predict the synthesis of the following molecule when the starting compound is 2,3-dimethylaniline.