Provide the complete mechanism using CAF for the reaction of aniline sequentially with (i) acetic anhydride, (ii) nitronium ion; (iii) aqueous base. Name the final product(s) formed.
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- Provide a mechanism for this sequence and the structure of intermediate A. Show all proton transfers.Draw a detailed mechanism for the reactions performed in this experiment, starting from p-vanillin and benzylamine and ending with the amine product (reductive amination of p-vanillin and benzylamine, resulting in the formation of 4-((benzylamino)methyl)-2-methoxyphenol.). plz answer in details. thanksGive a retrosynthetic analysis and suggest two synthesis of the target molecule (on the left) from the given starting material (on the right). (any reagents maybe used) . Give the full mechanism and include arrows
- Provide reasonable mechanisms for the following reaction.Suggest a reasonable mechanism for the conversion of a nitrile (RCN) to the corresponding amide in aqueous acid.Provide a detailed mechanism for the following (Hint:halohydrin reaction). Use arrows to show electron flow and show intermediates.