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- Hi,I need help with this chemistry question, please and thank you From the reaction between pyrrolidine and 2-methylcyclohexanone in an acid medium, enamines I and II can be formed. Describe which of the two is formed preferably and explain why?In synthesizing primary (1°) amines by alkylation of NH3, explain how we can prevent the formation of 2°and 3° amines as by-products? You can give an example to help you in explaining but it is not required. (please provide clear and complete explinationPlease don't provide handwritten solution ..... 2. Predicts the main organic product for the reaction:
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- Supply the product for the azo coupling between 4-nitroaniline and resorcinol. Explain brieflyDraw/outline a reasonable and detailed mechanism for the dehydration of 2-methylcyclohexanol catalyzed by phosphoric acid. Use curved arrows to show the flow of electrons and draw the structures of all intermediates and byproducts formed in the reaction. Predict and rationalize the expected product distribution based on thermodynamic aspectsIn preparation of p-Nitroaniline, Starting material is 50g of p-nitroacetanilide, 22ml of HCI, 20g of p-nitroaniline. Give % yield of nitro acetanilide. What is the objective of experiment? What is product prepared?