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- 3. Propose a mechanism for the following Sn1 reaction. Include structure for the carbocation intermediate. (0.5pts) o CI NaBr EtOH ∞or Br + NaCl(1R,2R)-1-Bromo-2-methylcyclopentane is reacted with sodium methoxide. Given the product(s) and show the reaction mechanism, including the depiction of the transition state. Draw an energy diagram for this conversion.Provide the product and a mechanism
- 2. Provide the reagents necessary to carry out the multistep syntheses shown below. (6+6) -Br Br -OH12B. CARBONYL REACTION MECHANISMS Draw the arrow-pushing mechanism for the reactions, including all charged intermediates and product. Mix & Match (Mechanism Bootcamp): draw the mechanism for each starting material (1-6) and reagent from the 12B reactions (previous page) (1a) NABH4 MeOHDraw the major organic product for the reactions