- The acid-dissociation constant for benzoic acid C6H5COOH is 6.3 * 10^-5. Calculate the equilibrium concentrations of H3O+, C6H5COO-, and C6H5COOH in the solution if the initial concentration of C6H5COOH is 0.050 M.
Problem 57
Problem 58
The acid-dissociation constant for chlorous acid 1HClO22 is 1.1 * 10-2. Calculate the concentrations of H3O+, ClO2-, and HClO2 at equilibrium if the initial concentration of HClO2 is 0.0125 M.
Problem 59a,b
Calculate the pH of each of the following solutions (Ka and Kb values are given in Appendix D): (a) 0.095 M propionic acid (C2H5COOH) (b) 0.100 M hydrogen chromate ion (HCrO4-)
Problem 60c
Determine the pH of each of the following solutions (Ka and Kb values are given in Appendix D): (c) 0.165 M hydroxylamine.
- Saccharin, a sugar substitute, is a weak acid with pKa = 2.32 at 25 °C. It ionizes in aqueous solution as follows: HNC7H4SO31(aq) ⇌ H+(aq) + NC7H4SO3-(aq). What is the pH of a 0.10 M solution of this substance?
Problem 61
- The active ingredient in aspirin is acetylsalicylic acid 1HC9H7O42, a monoprotic acid with Ka = 3.3 * 10^-4 at 25 °C. What is the pH of a solution obtained by dissolving two extra-strength aspirin tablets, each containing 500 mg of acetylsalicylic acid, in 250 mL of water?
Problem 62
- Calculate the percent ionization of hydrazoic acid (HN3) in solutions of each of the following concentrations (Ka is given in Appendix D): (a) 0.400 M, (b) 0.100 M, (c) 0.0400 M.
Problem 63
Problem 64
Calculate the percent ionization of propionic acid (C2H5COOH) in solutions of each of the following concentrations (Ka is given in Appendix D): (a) 0.250 M (b) 0.0800 M (c) 0.0200 M
Problem 65
Citric acid, which is present in citrus fruits, is a triprotic acid (Table 16.3). (a) Calculate the pH of a 0.040 M solution of citric acid. (b) Did you have to make any approximations or assumptions in completing your calculations? (c) Is the concentration of citrate ion 1C6H5O7 3-2 equal to, less than, or greater than the H+ ion concentration?
- Tartaric acid is found in many fruits, including grapes, and is partially responsible for the dry texture of certain wines. Calculate the pH and the tartrate ion C4H4O6²⁻ concentration for a 0.250 M solution of tartaric acid, for which the acid-dissociation constants are listed in Table 16.3. Did you have to make any approximations or assumptions in your calculation?
Problem 66
- Consider the base hydroxylamine, NH2OH. (c) There are two atoms in hydroxylamine that have nonbonding electron pairs that could act as proton acceptors. Use Lewis structures and formal charges (Section 8.5) to rationalize why one of these two atoms is a much better proton acceptor than the other.
Problem 67
Problem 67a
Consider the base hydroxylamine, NH2OH. (a) What is the conjugate acid of hydroxylamine?
Problem 68a
The hypochlorite ion, ClO-, acts as a weak base. (a) Is ClO- a stronger or weaker base than hydroxylamine?
Problem 68c
The hypochlorite ion, ClO-, acts as a weak base. (b) When ClO- acts as a base, which atom, Cl or O, acts as the proton acceptor? (c) Can you use formal charges to rationalize your answer to part (b)?
- Write the chemical equation and the Kb expression for the reaction of each of the following bases with water: (a) dimethylamine, (CH3)2NH (b) carbonate ion, CO3^2- (c) formate ion, CHO2^-
Problem 69
Problem 70a
Write the chemical equation and the Kb expression for the reaction of each of the following bases with water: (a) propylamine, C3H7NH2
Problem 70c
Write the chemical equation and the Kb expression for the reaction of each of the following bases with water: (c) benzoate ion, C6H5CO2-
- Calculate the molar concentration of OH- in a 0.075 M solution of ethylamine (C2H5NH2); Kb = 6.4 * 10^-4. Calculate the pH of this solution.
Problem 71
- Calculate the molar concentration of OH- in a 0.724 M solution of hypobromite ion BrO-; Kb = 4.0 * 10^-6. What is the pH of this solution?
Problem 72
Problem 73a
Ephedrine, a central nervous system stimulant, is used in nasal sprays as a decongestant. This compound is a weak organic base: C10H15ON1aq2 + H2O1l2 Δ C10H15ONH+1aq2 + OH-1aq2 A 0.035 M solution of ephedrine has a pH of 11.33. (a) What are the equilibrium concentrations of C10H15ON, C10H15ONH+, and OH-?
Problem 73b
Ephedrine, a central nervous system stimulant, is used in nasal sprays as a decongestant. This compound is a weak organic base: C10H15ON1aq2 + H2O1l2 Δ C10H15ONH+1aq2 + OH-1aq2 A 0.035 M solution of ephedrine has a pH of 11.33. (b) Calculate Kb for ephedrine.
Problem 74
Codeine 1C18H21NO32 is a weak organic base. A 5.0 * 10-3M solution of codeine has a pH of 9.95. Calculate the value of Kb for this substance. What is the pKb for this base?
- Phenol, C6H5OH, has a Ka of 1.3 * 10^-10. (c) Is phenol a stronger or weaker acid than water?
Problem 75
Problem 76
Use the acid-dissociation constants in Table 16.3 to arrange these oxyanions from strongest base to weakest: SO42-, CO32-, SO32-, and PO43-.
Problem 77a
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?
Problem 77b
Which is the stronger base, the acetate ion or the hypochlorite ion?
Problem 77c
Calculate Kb values for CH3COO- and ClO-.
Problem 78a
Given that Kb for ammonia is 1.8 × 10-5 and that for hydroxylamine is 1.1 × 10-8, which is the stronger base?
Problem 78b
Which is the stronger acid, the ammonium ion or the hydroxylammonium ion?
- Using data from Appendix D, calculate [OH-] and pH for each of the following solutions: (a) 0.10 M NaBrO (b) 0.080 M NaHS (c) a mixture that is 0.10 M in NaNO2 and 0.20 M in Ca(NO3)2.
Problem 79
Ch.16 - Acid-Base Equilibria