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- Provide the synthesis for the following product starting with the provide starting material. More than one step is required. Show the mechanism for each reaction. Please give details.Provide the structure of the enamine synthesized from the following reaction. O. COMe + H3O+ Provide the structures of the products and draw the complete curved arrow mechanism for the hydrolysis of the indicated acetal OR imine in aqueous acid. HN-CHO Reaction mechanism: [H+] OR Enamine N H3O+Provide the complete mechanism using curved arrow formalism for the reaction of p-isopropxlbenzoic acid undergoing nitration. Tell how many peaks in the 'H and 13C NMR spectrum that would be observed for the final product.
- draw a dehydration reaction and provide a detailed mechanism, explaining the formation of all possible products using appropriate chemical terminology.provide the mechanism given the product and starting material along with any reagents neededProvide the reagents and products for the nitration of toulene and explain why. Draw a detailed mechanism for the reaction