Consider the compound 2,3-dimethylhex-2-ene shown below. 2,3-dimethylhex-2-ene Design a synthesis likely to result in the formation of 2,3-dimethylhex-2-ene starting with 2-bromopentane and any other real reagents. Include all reagents and conditions. A mechanism is not required.
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- Ozonolysis of compound D will produce compound E and compound F as products. Hydrationof compound D will produce compound G as major product. Compound D is a major productobtained from dehydrohalogenation of 2-chloro-3-methylbutane. a) Identify the structural formula for compound D, E, F and G.b) Suggest suitable reagent(s) and condition(s) needed for dehydrohalogenation of 2-chloro-3-methylbutaneBelow are two potential methods for preparing the same ether (Option A and B), but only one of them is actually successful. Identify the successful approach (A or B)A key step in the synthesis of naproxen, an NSAID more commonly known by its brand name, Aleve (Section 3.9), is a coupling reaction of 2-bromo-6-methoxynaphthalene to form 2-methoxy-6-vinylnaphthalene. Show three different coupling reactions, and the required reagents, that could be used tocarry out this step.
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