Describe compound y absorbs 2 equivalents of hydrogen

Reference no: EM13332543

A.) Draw the structure(s) of the epoxide(s) you would obtain by formation of a bromohydrin from trans-3-heptene, followed by treatment with base. Use wedge and dash bonds to indicate stereochemistry and show both enantiomers if product is racemic. B.) Compound X, C14H12Br2, is optically inactive. On treatment with strong base, X gives hydrocarbon Y, C14H10. Compound Y absorbs 2 equivalents of hydrogen when reduced over a palladium catalyst to give Z (C14H14) and reacts with ozone to give one product, benzoic acid (C7H6O2). Draw the structure of compound Z

Reference no: EM13332543

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