12. Carbonated water has a [H+Jeg = 3.2 × 10-4 M; this is the result of thedissociation of carbonic acid:H₂CO3 (ag)H+ (aq) + HCO3- (ag)Kc = 4.4 x 10-7a. Set up the equilibrium constant expression for this acid dissociation.b. Calculate [H₂CO₂]ea. Hint: An ICE table may be handy.c. Carbonic acid is created by dissolving carbon dioxide in water. Given that theHenry's Law constant of carbon dioxide is 29.76 atm/M, what partial pressureof carbon dioxide is needed to make carbonated water?

a. The equilibrium constant expression for the acid dissociation reaction of carbonic acid is: Kc =…

12. Carbonated water has a [H+Jeg = 3.2 × 10-4 M; this is the result of the dissociation of carbonic acid: H₂CO3 (ag) H+ (aq) + HCO3- (aq) Kc = 4.4 x 10-7 a. Set up the equilibrium constant expression for this acid dissociation. b. Calculate [H₂CO3]ea. Hint: An ICE table may be handy. c. Carbonic acid is created by dissolving carbon dioxide in water. Given that the Henry's Law constant of carbon dioxide is 29.76 atm/M, what partial pressure of carbon dioxide is needed to make carbonated water?

12. Carbonated water has a [H+Jeg = 3.2 × 10-4 M; this is the result of the dissociation of carbonic acid: H₂CO3 (ag) H+ (aq) + HCO3- (aq) Kc = 4.4 x 10-7 a. Set up the equilibrium constant expression for this acid dissociation. b. Calculate [H₂CO3]ea. Hint: An ICE table may be handy. c. Carbonic acid is created by dissolving carbon dioxide in water. Given that the Henry's Law constant of carbon dioxide is 29.76 atm/M, what partial pressure of carbon dioxide is needed to make carbonated water?

Chemistry for Engineering Students

4th Edition

ISBN:9781337398909

Author:Lawrence S. Brown, Tom Holme

Publisher:Lawrence S. Brown, Tom Holme

Chapter12: Chemical Equilibrium

Section: Chapter Questions

Problem 12.65PAE

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Define or illustrate the meaning of the following terms: a. amphoteric b. Kw reaction c. Kw equilibrium constant d. pH e. pOH f. pKw Give the conditions for a neutral aqueous solution at 25C, in terms of [H+], pH, and the relationship between [H+] and [OH]. Do the same for an acidic solution and for a basic solution. As a solution becomes more acidic, what happens to pH, pOH, [H+], and [OH]? As a solution becomes more basic, what happens to pH, pOH, [H+], and [OH]?
Weak base B has a pKb of 6.78 and weak acid HA has a pKa of 5.12. a Which is the stronger base, B or A? b Which is the stronger acid, HA or BH+? c Consider the following reaction: B(aq)+HA(aq)BH+(aq)+A(aq) Based on the information about the acid/base strengths for the species in this reaction, is this reaction favored to proceed more to the right or more to the left? Why? d An aqueous solution is made in which the concentration of weak base B is one half the concentration of its acidic salt, BHCl, where BH+ is the conjugate weak add of B. Calculate the pH of the solution. e An aqueous solution is made in which the concentration of weak acid HA twice the concentration of the sodium salt of the weak acid, NaA. Calculate the pH of the solution. f Assume the conjugate pairs B/BH+ and HA/A are capable of being used as color-based end point indicators in acidbase titrations, where B is the base form indicator and BH is the acid form indicator, and HA is the acid form indicator and A is the base form indicator. Select the indicator pair that would be best to use in each of the following titrations: (1) Titration of a strong acid with a strong base. (i) B/BH+ (ii) HA/A (2) Titration of a weak base with a strong acid. (i) B/BH+ (ii) HA/A
Calculate [CO32] in a 0.010-M solution of CO2 in water (usually written as H2CO3). If all the CO32 in this solution comes from the reaction HCO3(aq)H+(aq)+CO32(aq) what percentage of the H+ ions in the solution is a result of the dissociation of HCO3? When acid is added to a solution of sodium hydrogen carbonate (NaHCO3), vigorous bubbling occurs. How is this reaction related to the existence of carbonic acid (H2CO3) molecules in aqueous solution?
Table 13-4 lists the stepwise Ka values for some polyprotic acids. What is the difference between a monoprotic acid, a diprotic acid, and a triprotic acid? Most polyprotic acids are weak acids; the major exception is H2SO4. To solve for the pH of a solution of H2SO4, you must generally solve a strong acid problem as well as a weak acid problem. Explain. Write out the reactions that refer to Ka1 and Ka2 for H2SO4. For H3PO4, Ka1 = 7.5 103, Ka2 = 6.2 108, and Ka3= 4.8 1013. Write out the reactions that refer to the Ka1, Ka2and Ka3equilibrium constants. What are the three acids in a solution of H3PO4? Which acid is strongest? What are the three conjugate bases in a solution of H3PO4? Which conjugate base is strongest? Summarize the strategy for calculating the pH of a polyprotic acid in water.
Composition diagrams, commonly known as alpha plots, are often used to visualize the species in a solution of an acid or base as the pH is varied. The diagram for 0.100 M acetic acid is shown here. The plot shows how the fraction [alpha ()] of acetic acid in solution, =[CH3CO2H][CH3CO2H]+[CH3CO2] changes as the pH increases (blue curve). (The red curve shows how the fraction of acetate ion, CH3CO2, changes as the pH increases.) Alpha plots are another way of viewing the relative concentrations of acetic acid and acetate ion as a strong base is added to a solution of acetic acid in the course of a titration. (a) Explain why the fraction of acetic acid declines and that of acetate ion increases as the pH increases. (b) Which species predominates at a pH of 4, acetic acid or acetate ion? What is the situation at a pH of 6? (c) Consider the point where the two lines cross. The fraction of acetic acid in the solution is 0.5, and so is that of acetate ion. That is, the solution is half acid and half conjugate base; their concentrations are equal. At this point, the graph shows the pH is 4.74. Explain why the pH at this point is 4 74.
Malic acid is a weak diprotic organic acid with Ka1 = 4.0 104 and Ka2 = 9.0 105. a Letting the symbol H2A represent malic acid, write the chemical equations that represent Ka1 and Ka2. Write the chemical equation that represents Ka1 Ka2. b Qualitatively describe the relative concentrations of H2A, HA, A2, and H3O+ in a solution that is about one molar in malic acid. c Calculate the pH of a 0.0175 M malic acid solution and the equilibrium concentration of [H2A]. d What is the A2 concentrationin in solutions b and c?
In dilute aqueous solution HF acts as a weak acid. However, pure liquid HF (boiling point = 19.5 C) is a strong acid. In liquid HF, HNO3 acts like a base and accepts protons. The acidity of liquid HF can be increased by adding one of several inorganic fluorides that ale Lewis acids and accept F- ion (for example, BF3 or SbF5]. Write balanced chemical equations for the reaction of pure HNO3 with pure HF and of pure HF with BF3.
Amino acids are an important group of compounds. At low pH, both the carboxylic acid group (CO2H) and the amine group (NHR) are protonated. However, as the pH of the solution increases (say, by adding base), the carboxylic acid proton is removed, usually at a pH between 2 and 3. In a middle range of pHs, therefore, the amine group is protonated, but the carboxylic acid group has lost the proton. (This is called a zwitterion.) At more basic pH values, the amine proton is dissociated. What is the pH of a 0.20 M solution of alanine hydrochloride, [NH3CHCH3CO2H]Cl?
Prove that Ka1 Kb2 = Kw for oxalic acid H2C2O4, by adding the chemical equilibrium expressions that corresponds to first ionization step of the acid in water with second step of the reaction of the fully deprotonated base, C2O42, with water.
Ionization of the first proton from H2SO4 is complete (H2SO4 is a strong acid); the acid-ionization constant for the second proton is 1.1 102. a What would be the approximate hydronium-ion concentration in 0.100 M H2SO4 if ionization of the second proton were ignored? b The ionization of the second proton must be considered for a more exact answer, however. Calculate the hydronium-ion concentration in 0.100 M H2SO4, accounting for the ionization of both protons.
Ionization of the first proton from H2SeO4 is complete (H2SeO4 is a strong acid); the acid-ionization constant for the second proton is 1.2 102. a What would be the approximate hydronium-ion concentration in 0.150 M H2SeO4 if ionization of the second proton were ignored? b The ionization of the second proton must be considered for a more exact answer, however. Calculate the hydronium-ion concentration in 0.150 M H2SeO4, accounting for the ionization of both protons.
Consider all acid-base indicators discussed in this chapter. Which of these indicators would be suitable for the titration of each of these? (a) NaOH with HClO4 (b) acetic acid with KOH (c) NH3 solution with HBr (d) KOH with HNO3 Explain your choices.