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- Name the structure. Heating compound A in the presence of H2SO4 results in which product?Hydrogenation of alkene A with D2 in the presence of Pd-C affords asingle product B. Keeping this result in mind, what compound is formedwhen A is treated with each reagent: (a) mCPBA; (b) Br2, H2O followedby base? Explain these results.provide the missing reagents as appropriate
- Draw the line structures of the products for a) and b) in the reactions below. No stereochenistry is required.Which of the following is/are the expected product/s of the reaction of 2-pentanone (CH3COCH2CH2CH3) with excess Br2, followed by OH-? CHBr3 + CH3CH2CH2COOH BrCH2COCH2CH2CH3 CHBr3 + CH3CH2CH2COO- CH3COCHBrCH2CH3"The following reactions DO NOT afford the product that is shwon. Concisely explain why this is so."