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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?a. Draw the structures of all the elimination products. b. The reaction occurs through an E2 mechanism. Using one of your products writethe mechanism of the reaction using curved arrows. c. Is this reaction regioselective? Explain your answer. d. Explain why the reaction is stereoselective.Draw the E1 (elimination) mechanism for the reaction
- A) what is the major product if E2 mechanism is followed in the reaction (A-D) B) what is the complete mechanism with steps to form the major productWhich of A to E shows the product that will be obtained from the reaction of (Z)-hex-2-ene with MeCO3H?Explain the Reaction of ROH with PBr3—An SN2 Mechanism