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: cyclohexanone (pK = 16.7), and ethylammonium ion (pKa = 10.8). H2 CH NH2 CH NH3 A в D ethylamine cyclohexanone ethylammonium cyclohexanone enolate a) The stronger base is b) Its conjugate acid is c) The species that predominate at equilibrium are (two letters, e.g. ac)

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Chapter1: Chemical Foundations
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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:
cyclohexanone (pK = 16.7), and ethylammonium
ion (pK = 10.8).
CH5
NH2
CH
ÑH3
A
в
D
ethylamine
cyclohexanone
ethylammonium
cyclohexanone
enolate
a) The stronger base is
b) Its conjugate acid is
c) The species that predominate at equilibrium are
(two letters, e.g. ac)
Transcribed Image Text: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: cyclohexanone (pK = 16.7), and ethylammonium ion (pK = 10.8). CH5 NH2 CH ÑH3 A в D ethylamine cyclohexanone ethylammonium cyclohexanone enolate a) The stronger base is b) Its conjugate acid is c) The species that predominate at equilibrium are (two letters, e.g. ac)
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