Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D below each. structure. A table of pKa values for various organic and inorganic acids can be found in the references section. NH₂ + A amide B ethyl acetate CH₂ NH₂ + C ammonia D ethyl acetate enolate CH₂ a) The weaker acid is b) Its conjugate base is c) The species that predominate at equilibrium are (two letters, e.g. AC)

Organic Chemistry
9th Edition
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Chapter20: Carboxylic Acids And Nitriles
Section20.4: Substituent Effects On Acidity
Problem 9P
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Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D below each
structure.
A table of pKa values for various organic and inorganic acids can be found in the references section.
NH₂
A
amide
B
ethyl acetate
NH₂
C
ammonia
D
ethyl acetate
enolate
a) The weaker acid is
b) Its conjugate base 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. A table of pKa values for various organic and inorganic acids can be found in the references section. NH₂ A amide B ethyl acetate NH₂ C ammonia D ethyl acetate enolate a) The weaker acid is b) Its conjugate base 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: ethanol (pK₂ = 16.0), and ethylammonium ion (pKa = 10.8).
CH₂
ethylammonium
NH₂
Submit Answer
+ CH₂
CH₂-SH
A
methanethiol
B
ethoxide
Submit Answer
a) The stronger acid is
b) Its conjugate base is
c) The species that predominate at equilibrium are (two letters, e.g. ac)
H₂
OH
B
hydroxide
NH₂
с
ethylamine
Retry Entire Group 7 more group attempts remaining
Retry Entire Group
CH₂-5
C
methanethiolate
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: water (pKa = 15.7), and methanethiol (pK₂ = 10.3).
+ HOH
•
D
water
a) The stronger base is
b) Its conjugate acid is
c) The species that predominate at equilibrium are (two letters, e.g. ac)
D
ethanol
7 more group attempts remaining
H₂
✔
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: ethanol (pK₂ = 16.0), and ethylammonium ion (pKa = 10.8). CH₂ ethylammonium NH₂ Submit Answer + CH₂ CH₂-SH A methanethiol B ethoxide Submit Answer a) The stronger acid is b) Its conjugate base is c) The species that predominate at equilibrium are (two letters, e.g. ac) H₂ OH B hydroxide NH₂ с ethylamine Retry Entire Group 7 more group attempts remaining Retry Entire Group CH₂-5 C methanethiolate 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: water (pKa = 15.7), and methanethiol (pK₂ = 10.3). + HOH • D water a) The stronger base is b) Its conjugate acid is c) The species that predominate at equilibrium are (two letters, e.g. ac) D ethanol 7 more group attempts remaining H₂ ✔
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