9. Draw the constitutional isomer formed when the following alkenes are treated with each set of reagents: [1] H20, H,SO4; or [2] BH3 followed by H2O2, "OH. A lo outouTC. vinmmoo 2wooo eloyoolertenig er besibhdvn mols W oso al waH a a. b. Seblagr motsis00 isq ool nope 2eob lsticho to egyt Jedw.nl.d Fnistnoo ennug 290b anodoglen ynam woHo
9. Draw the constitutional isomer formed when the following alkenes are treated with each set of reagents: [1] H20, H,SO4; or [2] BH3 followed by H2O2, "OH. A lo outouTC. vinmmoo 2wooo eloyoolertenig er besibhdvn mols W oso al waH a a. b. Seblagr motsis00 isq ool nope 2eob lsticho to egyt Jedw.nl.d Fnistnoo ennug 290b anodoglen ynam woHo
Chapter17: Alcohols And Phenols
Section17.SE: Something Extra
Problem 69AP: As a rule, axial alcohols oxidize somewhat faster than equatorial alcohols. Which would you expect...
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Here we have to find the major constitutional isomer formed in the following alkene substrate by hydration of alkene in acidic medium through formation of carbocation intermediate and by hydroboration - oxidation reaction of alkene. For unsymmetrical alkene different constitutional isomer will be formed depending the reagent participate in reaction.
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