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- Supply synthetic routes to the following molecules using the indicated starting materialsFor SN1 Explain the order in which 2o (secondary) alkyl halides reacted (fastest to slowest) and explain why. 2o (secondary) compounds listed are: (see picture) 2-chlorobutane 2-bromobutane bromobenzene bromocyclopentane bromocyclohexane Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature. Be sure to explain which alkyl halides did not react and whyGive the products of the reaction given below and state which reaction willproceed faster?
- Under second-order conditions (strong base/nucleophile), SN2 and E2 reactions may occur simultaneously and compete witheach other. Show what products might be expected from the reaction of 2-bromo-3-methylbutane (a moderately hindered 2°alkyl halide) with sodium ethoxide.provide the starting material using the product on the right. also provide the reagentsGive the missing reactants, reagent(s), conditions, and/or major product for the reactions below-