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Chapter 14/15 Review

Fill in the blanks:

Arrhenius defined acids as producing 1 in aqueous solution and bases as producing

2 in aqueous solution. The 3 definitions are more general: a(n) 4 is a proton donor

and a(n) 5 is a proton acceptor. Water is said to be 6 because it can act as either acid or

base. For strong acids and bases, the equilibrium lies far to the 7 . For weak acids and bases,

the K value is 8 . An acid containing more than one acidic proton is called 9 . The

concentrations of 10 and/or 11 ions in solution determines the pH, which is calculated by

12 .

13 can be acidic, basic, or neutral when dissolved in water. 14 is neutral when

dissolved in water. 15 is acidic when dissolved in water, and 16 is basic. When

determining pH of these solutions, a new K value must be calculated using the formula 17 .

The value of Kw is 18 .

When a weak acid and its conjugate base are dissolved in the same solution, a 19__

exists. This solution resists pH changes because the ratio of 20 is almost constant.

1. H+ / hydronium 11. OH–

2. OH– / hydroxide 12. pH = – log [H+]

3. Bronsted-Lowry 13. Salts

4. acid 14. NaCl (various answers)

5. base 15. NH4Cl (various answers)

6. amphoteric 16. NaCH3COO (various answers)

7. right 17. Ka x Kb = Kw

8. small 18. 1.0 x 10–14

9. polyprotic 19. buffer

10. H+ 20. [A–] : [HA]

Acid / Ka / Base / Kb
HClO2 / 1.2 x 10–2 / NH3 / 1.8 x 10–5
HF / 7.2 x 10–4 / CH3NH2 / 4.38 x 10–4
HNO2 / 4.0 x 10–4 / C6H5NH2 / 3.8 x 10–10
CH3COOH / 1.8 x 10–5 / C5H5N / 1.7 x 10–9
HOCl / 3.5 x 10–8 / (C2H5)2NH / 1.3 x 10–3
HCN / 6.2 x 10–10

1. Calculate the pH for 0.25 M solutions of the following:

a. Ba(OH)2

Ba(OH)2 → Ba2+ + 2 OH– [OH–] = 2 x 0.25 M = 0.50 M

pH = 13.70

b. LiCN

CN– + H2O D HCN + OH–

0.25 – x x x Kb = Kw = 1.0 x 10–14 = x2

Ka 6.2 x 10-10 0.25

x = [OH–] = 2.0 x 10–3 M pH = 11.30

c. C5H5N

C5H5N + H2O D C5H5NH+ + OH–

0.25 – x x x Kb = 1.7 x 10–9 = x2

0.25

x = [OH–] = 2.1 x 10–5 M pH = 9.31

d. NH4NO3

NH4+ D NH3 + H+

0.25 - x x x Ka = Kw = 1.0 x 10–14 = x2

Kb 1.8 x 10–5 0.25

x = [H+] = 1.2 x 10-5M pH = 4.93

2. Calculate the percent dissociation for a 0.35 M solution of hydrofluoric acid.

HF D H+ + F–

0.35 – x x x 7.2 x 10–4 = x2 x = [H+] = 1.6 x 10–2 M

0.35

1.6 x 10–2 M x 100 = 4.5%

0.35 M

3. The pH of a 0.063 M solution of HOBr is 4.95. Calculate Ka.

[H+] = 10–4.95 = 1.1 x 10–5 M

HOBr D H+ + OBr–

0.063 – 1.1 x 10–5 1.1 x 10–5 1.1 x 10–5 Ka = (1.1 x 10–5)2 = 2.0 x 10–9

0.063 – 1.1 x 10–5

4. Are solutions of the following salts acidic, basic, or neutral? For those which are not neutral,

write balanced equations for the reactions causing the solution to be acidic or basic.

a. KCl neutral d. KF basic

F– + H2O D HF + OH–

b. NaCH3COO basic e. NH4I acidic

CH3COO– + H2O D CH3COOH + OH– NH4+ D NH3 + H+

c. CH3NH3Cl acidic f. Mg(CN)2 basic

CH3NH3+ D CH3NH2 + H+ CN– + H2O D HCN + OH–

5. a. Calculate the pH of a solution which is 0.50 M CH3NH2 and 0.70 M CH3NH3Cl.

CH3NH2 + H2O D CH3NH3+ + OH–

0.50 – x 0.70 – x x

4.38 x 10–4 = 0.70 x x = [OH–] = 3.1 x 10–4 M pH = 10.50

0.50

b. Calculate the pH after 0.10 mol of NaOH is added to one liter of the above solution.

OH– + CH3NH3+ → CH3NH2 + H2O

0.10 0.70 0.50

-0.10 -0.10 +0.10

0 0.60 0.60 x = [OH–] = 4.38 x 10–4 M pH = 10.64

c. Calculate the pH after 0.10 mol of HCl is added to one liter of the solution in part a.

H+ + CH3NH2 → CH3NH3+

0.10 0.50 0.70 4.38 x 10–4 = 0.80 x x = [OH–]= 2.2 x 10–4 M

-0.10 -0.10 +0.10 0.40

0 0.40 0.80 pH = 10.34

6. The molar solubility of silver carbonate is 0.032 M. Calculate Ksp.

Ag2CO3(s) D 2 Ag+(aq) + CO32–(aq)

0 0

+ 2x + x x = 0.032 M

0.064 0.032

Ksp = (0.064)2 (0.032) = 1.3 x 10–4

7. Calculate the molar solubility of Ag2SO4 (Ksp = 1.5 x 10–5) in the following solutions:

(a) pure water

(b) 0.15 M Al2(SO4)3

(a) Ag2SO4(s) D 2 Ag+(aq) + SO42–(aq)

0 0

+2x +x

2x x (2x)2 x = 1.5 x 10–5

x = mol sol = 0.016 M

(b) Ag2SO4(s) D 2 Ag+(aq) + SO42–(aq)

0 0.45

+ 2x + x

2x 0.45 + x (2x)2 (0.45) = 1.5 x 10–5

x = 2.9 x 10–3 M

8. A solution of hydrochloric acid of unknown concentration was titrated with 0.10 M NaOH. If

a 100.-mL sample of the HCl solution required exactly 35.0 mL of the NaOH solution to reach

the equivalence point, what was the pH of the HCl solution?

(M of HCl) (100. mL) = (0.10 M) (35.0 mL)

M of HCl = 0.035 M pH = 1.46

9. A 400.0 mL sample of 0.100 M acetic acid is titrated with 0.200 M NaOH. Calculate the pH

after the addition of the following volumes of base.

a. 30.0 mL c. 200.0 mL

b. 100.0 mL d. 300.0 mL

a. [CH3COOH] = (0.100 M)(400.0 mL) / (430.0 mL) = 0.0930 M

[OH–] = (0.200 M)(30.0 mL) / (430.0 mL) = 0.0140 M

CH3COOH + OH– → CH3COO– + H2O

0.0930 0.0140 0

– 0.0140 –0.0140 + 0.0140

0.0790 0 0.0140

CH3COOH D CH3COO– + H+

0.0790 0.0140 x 0.0140 x = 1.8 x 10–5

0.0790

x = [H+] = 1.0 x 10–4 M pH = 3.99

b. [CH3COOH] = (0.100 M)(400.0 mL) / (500.0 mL) = 0.0800 M

[OH–] = (0.200 M)(30.0 mL) / (500.0 mL) = 0.0400 M

half-equivalence point: pH = pKa = 4.74

c. [CH3COOH] = (0.100 M)(400.0 mL) / (600.0 mL) = 0.0667 M

[OH–] = (0.200 M)(30.0 mL) / (600.0 mL) = 0.0667 M

CH3COOH + OH– → CH3COO– + H2O

0.0667 0.0667 0

– 0.0667 –0.0667 + 0.0667

0 0 0.0667

CH3COO– + H2O D CH3COOH + OH–

0.0667 x x x2 = 1.0 x 10–14

0.0667 1.8 x 10–5

x = [OH–] = 6.1 x 10–6M pH = 8.78

d. [CH3COOH] = (0.100 M)(400.0 mL) / (700.0 mL) = 0.0571 M

[OH–] = (0.200 M)(30.0 mL) / (700.0 mL) = 0.0857 M

CH3COOH + OH– → CH3COO– + H2O

0.0571 0.0857 0

– 0.0571 –0.0571 + 0.0571

0 0.0286 0.0571 [OH–] = 0.0286 M pH = 12.457

10. Consider the titration of 100.0 mL of 0.100 M HCl by 0.200 M NaOH. Calculate the pH of

the resulting solution after each of the following volumes of NaOH has been added.

a. 0.0 mL c. 50.0 mL

b. 30.0 mL d. 75.0 mL

a. 0.100 M H+ pH = 1.000

b. [H+] = (0.100 M)(100.0 mL) / (130.0 mL) = 0.0769 M

[OH–] = (0.200 M)(30.0 mL) / (130.0 mL) = 0.0462 M

H+ + OH– → H2O

0.0769 0.0462

–0.0462 –0.0462

0.0307 0 [H+] = 0.0307 M pH = 1.513

c. [H+] = (0.100 M)(100.0 mL) / (150.0 mL) = 0.0667 M equivalence point

[OH–] = (0.200 M)(30.0 mL) / (150.0 mL) = 0.0667 M pH = 7.000

d. [H+] = (0.100 M)(100.0 mL) / (175.0 mL) = 0.0571 M

[OH–] = (0.200 M)(30.0 mL) / (175.0 mL) = 0.0857 M

H+ + OH– → H2O

0.0571 0.0857

–0.0571 –0.0571

0 0.0286 [OH–] = 0.0286 M pH = 12.457