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- Give a complete arrow-pushing mechanism for the following reactions. Show all important resonance structures of the intermediates and show exactly where each proton comes from and goes to. Indicate the Lewis acid and Lewis base (LA or LB) and whether they are also Bronsted acids and bases (BA or BB) for each intermolecular reaction. To preview image Click Here. EtOH HCI (cat.) OEt OEt H₂ODraw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side product is continuously removed to drive the reaction toward products. (CH2OH)2, TSOH P Type here to searchDraw the major product of this reaction. Ignore inorganic byproducts. Explain.
- Draw the major product of this reaction. Ignore inorganic byproducts. H3O*, heat P Type here to searchThe product in this reaction is basic enough to be protonated by a dilute HCl solution. Draw the protonated species, clearly showing where protonation occurs. Draw all possible resonance structures of the conjugate acid of the product, and use these to explain why the product is so much more basic than a typical ester, like ethyl acetate.Draw the detailed reaction mechanism for the reaction below (remember to add the step where the carboxylate is protonated by HCl)
- Complete the reaction wheels below. For the starred reactions, draw the full reaction mechanism. Once complete, compare and contrast the common reactions shared by acyl halides and acid anhydrides.I need help with explaining on how to draw the final product or products to these reactions.Draw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. ] NaH OH