Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D below each structure. The pKa's forthe acids of interest are: diisopropylamine(pK-40), and t-butanol(pK,-18.0).CH3OHCH3CH3CHCH3C.CHCH3CH.CH3CH3CH3CH3CHSCH3CH3CH3D.Adiisopropylamidet-butanoldiisopropylaminet-butoxidea) The stronger base isb) Its conjugate acid isc) The species that predominate at equilibrium are (two letters, e.g. ac)5 more group attempts remainingRetry Entire GroupSubmit Answer

Answer a) The stronger base is D b) Its conjugate acid is A c) The species that predominates at…

Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D below each structure. The pKa's for the acids of interest are: diisopropylamine(pK-40), and t-butanol(pK,-18.0). CH3 CH3 OH CH3 CH3 CH CH CH CH CHs CH, N CH3 CH CH3 CHs CH ČH3 CH diisopropylamine t-butoxide t-butanol diisopropylamide a) The stronger base is b) Its conjugate acid is c) The species that predominate at equilibrium are (two letters, e.g. ac)

Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D below each structure. The pKa's for the acids of interest are: diisopropylamine(pK-40), and t-butanol(pK,-18.0). CH3 CH3 OH CH3 CH3 CH CH CH CH CHs CH, N CH3 CH CH3 CHs CH ČH3 CH diisopropylamine t-butoxide t-butanol diisopropylamide a) The stronger base is b) Its conjugate acid is c) The species that predominate at equilibrium are (two letters, e.g. ac)

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter20: Carboxylic Acids And Nitriles

Section20.4: Substituent Effects On Acidity

Problem 9P

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