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- Between E1 and E2, which reaction mechanism is most efficient to synthesize the (E) stereoisomer of this product on an industrial scale?Provide the mechanism for the conversion shown below. CH3Li is effectively H3C-Li+. What type of mechanism is occuring?What is the mechanism and product for the following reaction?
- Can you provide a mechanism for this reaction to show the major diastereoisomer that would be formed?Between E1 and E2, which reaction mechanism is more efficient to synthesize the (E) stereoisomer of this product on a large scale?Azo coupling reaction. Provide a mechanism with intermediates and arrows
- Please draw the mechanism for the following reaction. The first step in the reaction mechanism is the formation of a carbocation intermediate (shown), followed by a carbocation rearrangement. Which bond moves in the carbocation rearrangement? Which compound shown below has that appropriate bond in pink?( complete the reaction with mechanism , do 2st one )is this an E1 or E2 mechanism for this reaction? What is the major product and mechanism for it?