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- Name the following amine, including R, S stereochemistry, and draw the product of its reaction with excess iodomethane followed by heating with Ag2O (Hofmann elimination). Is the stereochemistry of the alkene product Z or E? Explain.When a cyclic ketone reacts with diazomethane, the next larger cyclic ketone is formed. This is called a ring-expansion reaction. Draw a mechanism forthe following ring-expansion reaction.Predict the products from reaction of 2-hexyne with the following reagents:(a) 2 equiv Br2(b) 1 equiv HBr(c) Excess HBr(d) Li in NH3(e) H2O, H2SO4, HgSO4
- The Knoevenagel reaction is a carbonyl condensation reaction of an ester with an aldehyde or ketone to yield an α, β-unsaturated product. Show the mechanism for the Knoevenagel reaction of diethyl malonate with benzaldehyde.What product is formed after 2 reactions (dilute acid then HIO4, H2SO4)?3 What are the products of reactions of aldhydes and ketones with (I) chloroform (ii) primary amines? No reagent or reaction condition given
- QUESTION 4Predict the products(s) from the reaction of 1-hexyne with each of the following reagents:a) 1 mole of HBrb) H2O, H2SO4, HgSO4c) 2 moles of Br2d) Excess Cl2e) 2 moles of HCl with H2O2f) 1 mole of HClusing any necessary reactants and reagents, propose reasonable syntheses of the following compounds from cyclohexanone can you please help with coumpound 3 (I attached it below). Thank you!dedcue the major organic product from the following reations. be ablw to draw hydration halogenation hydrohalogenation, halohydrin formation, oxymercuratiom demercuration qnd hydroboration oxidation.