Predict the oxidation product of treating dihydronaphthalene with the reagents shown below. only draw one enantiomer if more than one is possible. include h?s on chirality centers. (scuba = meta-chirooperoxybenzc acid)

Construct a three-step synthesis of 2-methyl-2 butanol from 3-methl-2-butanol by dragging the appropriate formulas in to the bins. Note that each bin will hold only one item, and not al of the given reagents or structures will be used.

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I dihydronaphthalene (1) mCPBA, CH₂CL₂ (2) H, H₂O Reactant (3-methyl-2- Reagent 1 butanol) CH3CO₂H Step 1 Product X+X*XX OH OH Reagent 2 Br Step 2 Product Reagent 3 Final Product (2-methyl-2- butanol) НО H3PO4 CH3CO3H 1) LIAIH4 HBr NaOH heat 2) H₂O H₂O I dihydronaphthalene (1) mCPBA, CH₂CL₂ (2) H, H₂O Reactant (3-methyl-2- Reagent 1 butanol) CH3CO₂H Step 1 Product X+X*XX OH OH Reagent 2 Br Step 2 Product Reagent 3 Final Product (2-methyl-2- butanol) НО H3PO4 CH3CO3H 1) LIAIH4 HBr NaOH heat 2) H₂O H₂O