Predict the product for the following reaction. H₂C H A) I and II B) II C) I (D) IV I E) III cis-1-bromo-3-methylcyclohexane SH H₂C || H H3C II|ISH H E III NaSH acetone Br H₂C xxx ISH IV H
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- cis-4-Bromocyclohexanol and trans-4-bromocyclohexanol form the same elimination product but a different substitution product when they reactwith HO-. a. Why do they form the same elimination product?b. Explain, by showing the mechanisms, why different substitution products are obtained.c. How many stereoisomers does each of the elimination and substitution reactions form?The reaction CH3-CH=CH-CH3 CH3CH(I)CH(I)CH3 can be achieved withcis-4-Bromocyclohexanol and trans-4-bromocyclohexanol form the same elimination product but a different substitution product when they react with HO-. a. Why do they form the same elimination product? b. Explain, by showing the mechanisms, why different substitution products are obtained. c. How many stereoisomers does each of the elimination and substitution reactions form?
- reactions and products for C9H8O4 C9H8O4 + O2 --> C9H8O4 + H2O --> C9H8O4 + HCl --> C9H8O4 + OH- --> C9H8O4 + Na --> C9H8O4 + F -->For each reaction, decide whether substitution or elimination (or both) is possible, andpredict the products you expect. Label the major products. chlorocyclohexane + NaOCH3 in CH3OHWhen 2-cyclobutylpropan-2-ol is treated with a solution of HBr in Et2O, 2-bromo-1,1-dimethylcyclopentane is the resulting product. Write the reaction and propose a mechanism using curved arrows notation in each step.
- Which reactant yeilds a single product and whyExplainwhythefollowingdeuterated1-bromo-2-methylcyclohexaneundergoes dehydrohalogenation by the E2 mechanism, to give only the indicated product. Two other alkenes are not observed.optically active 2- butanole slowly becoms racemic whem treated with with dilute acid > explain why