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- Write the mechanism for the following reactions. Explain detail each steps of reactions.For each reaction, give the expected substitution product, and predict whether the mechanism will be predominantly first order (SN1) or second-order (SN2). (a) isobutyl bromide + sodium methoxideFor each reaction, give the expected substitution product, and predict whether the mechanism will be predominantly first order (SN1) or second order (SN2). (a) cyclohexyl bromide + methanol
- ) Provide a reaction mechanism for the following reactions and name the major product for each. HBr H,SO4 HO,give the mechanism of the following reactions and explain why any selectivities occur.For each reaction, give the expected substitution product, and predict whether the mechanism will be predominantly first order (SN1) or second-order (SN2). (a) cyclohexyl bromide + sodium ethoxide
- (d) (i) Identify products B-F in the following reaction scheme. (ii) Provide a mechanism for the formation of B from benzene. (iii) Provide a mechanism for the formation of C from B. H2SO4 Brz B C FeBr3 Brz FeBrз H2SO4 D E & FStarting with benzene and using any other necessary reagents of your choice, create a synthesis (or sytheses) for each of the following compounds.The following compound is undergo ether cleavage with strong acid. OCH3 2 HBr N + P i) Draw the correct structure of compound N and P. ii) Write a complete ether cleavage reaction mechanism to produce compound N and P.
