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- 1. Provide the mechanism of the reaction shown in the picture. 2. Explain why it cannot be done in basic conditions. 3. Why is the enol tautomer favored over the keto tautomer? Ph H3C OH H H3O+/H₂O HO H3C PhAlkyl diazonium salts decompose to form carbocations, which go on to form products of substitution, elimination, and (sometimes) rearrangement. Keeping this in mind, draw a stepwise mechanism that forms all of the following products.1. Provide the mechanism of the reaction shown in the picture. 2. Explain why it cannot be done in basic conditions. 3. Why is the enol tautomer favored over the keto tautomer?
- Come up with a reasonable mechanism for the following reactionPlease provide the major product of the following reaction via an E2 mechanism. ... Br KO Bu (one equivalent) t-BuOHProvide 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+
- Alkyl diazonium salts decompose to form carbocations, which go on to form products of substitution, elimination, and (sometimes)rearrangement. Keeping this in mind, draw a stepwise mechanism thatforms all of the following productsPropouse a mechanism for the following reaction.Draw a detailed mechanism showing the formation of all products, be sure to draw all intermediate and show the movement of electros by arrows. F. F. F. -Br -OCH3 -OCH3 Heat
- Draw a stepwise, detailed mechanism for the following reaction. Show all intermediates involvedOchem help... What is the major product of the following reaction sequence? Provide the stepwise mechanism for each step (1, 2a, and 2b). (see attached image)Draw the mechanism for the following reaction. Provide all resonance structures for the arenium ion intermediate. F HNO3 H₂SO4 NO ₂