Answer Happy

Select the reagent that you would use to convert an alkene to a Markovnikov (more substituted) alcohol without possibility of carbocation rearrangement. O H2SO4, H2O O OSO4, TBHP, H2O O Hg(OAc)2, H2O, then NaBH4 O BH3-THF, then H2O2, H2O, NaOH
What is the stereochemical outcome of this reaction? 1. BH3-THF 2. H₂O2, NaOH (aq) a single chiral molecule enantiomers, equal amounts a single achiral molecule diastereomers, equal amounts enantiomers, unequal amounts diastereomers, unequal amounts product(s)
Which of these carbocations, as drawn, is the most stable? (Consider only these structures, not possible rearrangements that could occur.) OD O C O A B A 3 C