3 Revlew Tepics)LaterncasCH3CH,1. BH, THF2 NaOH, HO, H0,H,COHCH2H,CAlkenes can be hydrated via the addition of borane to yield alcohols with non-Markovnikov regiochemistry. The boron atom is an electrophile and thus followsMarkovnikov's rule in adding to the carbon containing the most hydrogens. Oxidation of the alkylborane with basic peroxide yields the product alcohol.Draw curved arrows to show the movement of electrons in this step of the mechanism.Arrow-pushing InstructionsEX+ UUR-B-0-R. Mavi Teits)haturncesCH,CH,1. BH, THE2. NaOH, HO, H,0,OHH;CCH2Alkenes can be hydrated via the addition of borane to yield alcohols with non-Markovnikov regiochemistry, The boron atom is an electrophile and thus folowsMarkovnikov's rule in adding to the carbon containing the most hydrogens. Oxidation of the alkylborane with basic peroxide yields the product alcohol.Draw curved arrows to show the movement of electrons in this step of the mechanism.Arrow pushing InstructionsEX-- UUCHCH,H-OHOH "OHSubmit AnserRtry Etire Groupmere greup atete remaining

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Masle Tepico hateancas CH, CH, 1. BH,, THE 2. NaOH, H,O, H0, H,C CH2 H,C Alkenes can be hydrated via the addition of borane to yield alcohols with non-Markovnikov regiochemistry. The boron atom is an electrophile and thus follows Markovnikov's rule in adding to the carbon containing the most hydrogens. Oxidation of the alkylborane with basic peroxide yields the product alcohol. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions

Masle Tepico hateancas CH, CH, 1. BH,, THE 2. NaOH, H,O, H0, H,C CH2 H,C Alkenes can be hydrated via the addition of borane to yield alcohols with non-Markovnikov regiochemistry. The boron atom is an electrophile and thus follows Markovnikov's rule in adding to the carbon containing the most hydrogens. Oxidation of the alkylborane with basic peroxide yields the product alcohol. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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A chemist allows some pure (2S,3R)-3-bromo-2,3-diphenylpentane to react with a solution of sodium ethoxide(NaOCH2 CH3) in ethanol. The products are two alkenes: A (cis-trans mixture) and B, a single pure isomer. Under the same conditions, the reaction of (2S,3S)-3-bromo-2,3-diphenylpentane gives two alkenes, A (cis-trans mixture) and C. Upon catalytic hydrogenation, all three of these alkenes (A, B, and C) give 2,3-diphenylpentane. Determine the structures of A, B, and C; give equations for their formation; and explain the stereospecificity of these reactions.
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