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- 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.Indicate the complete mechanisms for each step of the synthesis below.Illustrate detailed mechanisms and draw Product Z that could be obtained from the reaction below.
- write out a complete mechanism for the reaction below1. Discuss the role of the Aldol condensation reaction in the synthesis below. What specific reaction was used in the synthesis? What is the importance of the aldol reaction in the entire synthetic approach? 2. Show the detailed reaction mechanism involved in their corresponding specific parts in this syntheses.Please describe the difference in the outcome of treating a terminal alkyne with HgSO4, H2SO4, H2O and with 9-BBN, followed by H2O2 and NaOH.
- Please provide a mechanism with curved arrows by replacing MgBr with 3-methoxyphenylmagnesium bromide and the final product should be 3-methoxybenzoic acidProvide the synthetic route for the following reaction? (CH3)2CHCH2Br ----> (CH3)2CHCH2CH2CH2NH2Devise a detailed mechanism for formation of the major product of the elimination reaction below.
- Propose a reasonable mechanism for dihydroxylation with oxone (you may start with dimethyldioxirane, DMDO) that would lead to formation of a mixture of the cis- and trans-diols.What is the main product from the reaction sequence below?Fill in the missing reagent/product(s) for the following reactions.