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b Write a mechanism for the reaction using curved arrows to show electron reorganization. Consult the arrow-pushing instructiDraw the organic product of the following reaction. CH3 meta-Chloroperoxy- benzoic acid • You do not have to consider stereocCH3 CH3CH2CH2CH2CHCH2OH Can this alcohol be synthesized selectively by hydroboration-oxidation of an alkene? • If yes, draw t

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Answer #1

alkene reacts with BH3 and forms the syn addition product

alkene reacts with mCPBA and forms the epoxide

alkene undergoes the hydroboration oxidation and forms the anti markownikovs product
PH Xm Sypadriton meka chooperang beuroi Aid CH2 (mce C) CHE CH3-CH2-CH₂-CH₂ – CH=CH2-OH DBH2 THE 2) H2O2, NOOH CH3-CH2-CH₂-CH

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