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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: ammonia (pK, = 36), and acetone (pK, = 19.3). "NH2 CH CH3 NH3 CH3 A D acetone enolate amide acetone ammonia a) The stronger 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: phenol (pK = 9.9), and acetic acid (pK, = 4.8). он CH3- CH3- OH A в D acetate phenol acetic acid phenoxide a) The stronger 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: acetic acid (pK = 4.8), and hydrogen bromide (pK = -9). %3D Br CH3 CH3- + + H-Br OH A D acetic acid bromide acetate hydrogen bromide a) The stronger acid is HBr b) Its conjugate base is Br- c) The species that predominate at equilibrium are (two letters, e.g. ac) ad Submit Answer Retry Entire Group 9 more group attempts remaining Previous Next
- 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: ethylammonium ion (pK = 10.8), and hydrogen chloride (pKa = -7). CH3- NH2 CH3. NH3 cī H-CI H2 A в D chloride ethylamine hydrogen chloride ethylammonium a) The stronger 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 ✔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 (pK,=16.0), and benzoic acid (pK,=4.2). HO CH3 но CH3 A D benzoic acid ethoxide benzoate ethanol a) The stronger base is b) Its conjugate acid is c) The species that predominate at equilibrium are (two letters, e.g. ac) Submit Answer Retry Entire Group 5 more group attempts remaining Previous Next Email Instructor Save and Exit fo
- 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: ethene (pKa = 44), and ethanol (pKa = 16.0). %3D H2 CH3 H2C=CH2 CH HO, H,C=CH A D ethoxide ethene ethanol ethene anion a) The stronger acid is b) Its conjugate base is c) The species that predominate at equilibrium are (two letters, e.g. ac) Submit Answer Retry Entire Group 9 more group attempts remaining Previous Next Email Instructor Save and ExitAnswer 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: carbonic acid (pK, = 6.4), and acetic acid (pK, = 4.8). CH3 CH3- но но HO. OH A в acetic acid bicarbonate acetate carbonic acid a) The stronger base is b) Its conjugate acid is c) The species that predominate at equilibrium are (two letters, e.g. ac) Submit Answer Retry Entire Group 7 more group attempts remaining Previous Next Email Instructor Save and ExitAnswer 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: hydrogen cyanide (pK = 9.3), and pyridinium ion (pK = 5.2). %3D H-CN :CN H. A в hydrogen cyanide pyridine cyanide pyridinium a) The stronger acid is b) Its conjugate base is c) The species that predominate at equilibrium are (two letters, e.g. ac) Submit Answer Retry Entire Group 7 more group attempts remaining Previous Next
- 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: carbonic acid (pK₂ = 6.4), and anilinium ion (pK₂ = 4.6). NH₂ HO bicarbonate 9-19 HO с carbonic acid B :CN A cyanide anilinium OH a) The stronger acid is A b) Its conjugate base is C c) The species that predominate at equilibrium are (two letters, e.g. ac) AC B hydronium D aniline Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D below each structure. A table of pK₂ values for various organic and inorganic acids can be found in the references section. H-CN + с hydrogen cyanide D water NH₂ a) The weaker base is B b) Its conjugate acid is c c) The species that predominate at equilibrium are (two letters, e.g. AC) BCAnswer 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 (pK, = 16.0), and bicarbonate ion (pK,a = 10.3). CH HO, но CH3 A carbonate ethanol bicarbonate ethoxide 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: methanethiol (pKa = 10.3), and benzoic acid (pK, = 4.2). OH CH3-S CH3-SH A benzoic acid methanethiolate benzoate methanethiol a) The stronger base is b) Its conjugate acid is c) The species that predominate at equilibrium are (two letters, e.g. ac)