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- Predict the products of the following reactions. Include stereochemistry when necessary. For reactions with more than one step show the product formed after each step.Predict the products of the following reaction. Include stereochemistry when necessary. For reactions with more than one step show the product formed after each step.Predict the major products of the following reactions. Include appropriate stereochemistry in the product structures. S-1,3-dimethylcyclohexene + aqueous Hg(OAc)2Hg(OAc)2 followed by treatment with NaBH4
- Predict the products of reaction of pent-1-yne with the following reagents. H2SO4>HgSO4, H2OPredict the products of reaction of pent-1-yne with the following reagents. Na, liquid ammoniaPredict the major products of the following reactions, including stereochemistry.(a) cyclohexene + KMnO4>H2O (cold, dilute)
- Which of the alkenes below is the most reactive towards acid-catalyzed hydration?Predict the products of the following reactions. 2-ethoxy-2-methylpentane + concd. HBr, heatPredict the major products of the following reactions.a.4@chlorocycloheptene + Hg(OAc)2 in CH3OH b.the product from part (c), treated with NaBH4
- Give all the monobromination products of 2-methylpropane (or isobutane) in presence of heat or energy. Identify the major product and propose a mechanism leading to the formation of the major product. Provide a reaction in the termination step.Predict the major products of the following reactions. o@xylene + H2 (1000 psi, 100 °C, Rh catalyst)It is not uncommon for organic chemists to prepare acetals by an exchange-type process known as transacetalization. Predict the product(s) and show the mechanism for the transacetalization reactions below.