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- 2 CH3COOCH,CH3 C2H5O'K*/C2H5OH ---> CH3COCH,COOCH,CH3 [+] Hofmann elimination Clemmensen reduction Claisen condensation O Cannizzaro reaction O Aldol condensationWhy won't most primary alkyl halides react in Friedel-Crafts alkylation reactions? O Primary alkyl halides undergo methyl shifts under the standard conditions of Friedel-Crafts alkylation reactions, making them unreactive. Primary alkyl halides create primary carbocations which are too high in energy and too readily undergo rearrangement. Primary alkyl halides do not form a sigma complex after a nucleophilic attack since they connect at the primary carbocation site. Primary alkyl halides as a reactant violates one of the three standard limitations to Friedel-Crafts alkylation reactions.Draw the major organic product(s) of the following reaction. H3C-Bri NaOH
- Draw the major product of the reaction. OH NaH H2 NaBr + C6H100 DMF "Br +Draw Intermediate CH3OH₂+ protonation H H3C -0 H Q CH3OH deprotonation loss of H₂O elimination H3C :0 ÖH -CH3 Draw Intermediate CH3OH deprotonatio Please select a drawing or reagDraw the major product for the following transformation. O2N. Meo `CO2CH3