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). OH CH3 но CH3 A 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
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Q: Answer questions a-c about the Bronsted acid-base reaction below using the identifying letters A-D…
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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: 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)11) For the following reaction, identify the Lewis acid and the Lewis base and draw the curved arrow mechanism. H H -N - +) NH2 lewis base lewis Aciol SHN pinb!7 (P 12) Which of the following solvents can be used with NaNH2 and why? 02H (2 (9 HOʻHO H A.In the reaction CH3 COOH+H₂O=H3O++CH3 COO- the base constant K₁ of the acetate ion CH3COO is approximately 10-⁹ at 25 °C. What is the pk of acetic acid, CH3COOH? a (A) 10-⁹ (B) 9 (C) -5 (D) 5 (E) 10-5
- Low-molecular-weight dicarboxylic acids normally exhibit two different pK, values. Ionization of the first carboxyl group is easier than the second. This effect diminishes with molecular size, and for adipic acid and longer chain dicarboxylic acids, the two acid ionization constants differ by about one pK unit. Dicarboxylic Acid Structural Formula pK,2 a1 Охalic НООССООН 1.23 4.19 Malonic НООСCH,COOH 2.83 5.69 Succinic HOOC(CH,),COOH 4.16 5.61 Glutaric HOOC(CH,),COOH 4.31 5.41 Adipic HOOC(CH,),COOH 4.43 5.41 Why do the two pK, values differ more for the shorter chain dicarboxylic acids than for the longer chain dicarboxylic acids?Benzoic acid(C6H5-COOH) is a weak acid(pKa=4.2) and naphthalene is neutral, neither acidic or basic. Prepare a flowchart for the separation and recovery of benzoic acid and naphthalene.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 hydrogen cyanide (pK₂=9.3). Question 8a H-CN hydrogen cyanide B ethoxide :CN с cyanide 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
- 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: 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)PQ-23. At 298 K, the equilibrium constant for this reaction H2(g) + O2(g)= H₂O(l) AG° (kJ mol¹) -237 -229 H₂O(1) H₂O(g) (A) has a value of 1.0 at equilibrium. (B) is larger than the Keq for H2(g) + O2(g)=H₂O(g). (C) cannot be computed since data on O2 and H2 are not provided. (D) will have the same value as the Keq for H2(g) + O2(g)= H₂O(g)
- Given that Ka for acetic acid is 1.8 * 10-5 and that for hypochlorous acid is 3.0 * 10-8, which is the stronger acid?1a) Consider the reaction AH(+) + H₂O A: + H3O+). For the following named acids: a) draw the structure of the acid, b) give the approximate pKa of the conjugate acid in units of 5, c) give the name of the conjugate base, and d) draw the structure of the conjugate base. p-Toluenesulfonic acid acid Conjugate base Imidazolium cation pka_ pKa iso-Propanol pKa Acetylene pKaAnswer 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 Exit