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CHM 112 Summer 2007 M. Prushan Acid-Base Equilibria and Solubility Equilibria Chapter 16.

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Presentation on theme: "CHM 112 Summer 2007 M. Prushan Acid-Base Equilibria and Solubility Equilibria Chapter 16."— Presentation transcript:

1 CHM 112 Summer 2007 M. Prushan Acid-Base Equilibria and Solubility Equilibria Chapter 16

2 CHM 112 Summer 2007 M. Prushan The common ion effect is the shift in equilibrium caused by the addition of a compound having an ion in common with the dissolved substance. The presence of a common ion suppresses the ionization of a weak acid or a weak base. Consider mixture of CH 3 COONa (strong electrolyte) and CH 3 COOH (weak acid). CH 3 COONa (s) Na + (aq) + CH 3 COO - (aq) CH 3 COOH (aq) H + (aq) + CH 3 COO - (aq) common ion

3 CHM 112 Summer 2007 M. Prushan Consider mixture of salt NaA and weak acid HA. HA (aq) H + (aq) + A - (aq) NaA (s) Na + (aq) + A - (aq) K a = [H + ][A - ] [HA] [H + ] = K a [HA] [A - ] -log [H + ] = -log K a - log [HA] [A - ] -log [H + ] = -log K a + log [A - ] [HA] pH = pK a + log [A - ] [HA] pK a = -log K a Henderson-Hasselbalch equation pH = pK a + log [conjugate base] [acid]

4 CHM 112 Summer 2007 M. Prushan What is the pH of a solution containing 0.30 M HCOOH and 0.52 M HCOOK? HCOOH (aq) H + (aq) + HCOO - (aq) Initial (M) Change (M) Equilibrium (M) 0.300.00 -x-x+x+x 0.30 - x 0.52 +x+x x0.52 + x Common ion effect 0.30 – x  0.30 0.52 + x  0.52 pH = pK a + log [HCOO - ] [HCOOH] HCOOH pK a = 3.77 pH = 3.77 + log [0.52] [0.30] = 4.01 Mixture of weak acid and conjugate base!

5 CHM 112 Summer 2007 M. Prushan A buffer solution is a solution of: 1.A weak acid or a weak base and 2.The salt of the weak acid or weak base Both must be present! A buffer solution has the ability to resist changes in pH upon the addition of small amounts of either acid or base. Add strong acid H + (aq) + CH 3 COO - (aq) CH 3 COOH (aq) Add strong base OH - (aq) + CH 3 COOH (aq) CH 3 COO - (aq) + H 2 O (l) Consider an equal molar mixture of CH 3 COOH and CH 3 COONa

6 CHM 112 Summer 2007 M. Prushan Which of the following are buffer systems? (a) KF/HF (b) KBr/HBr, (c) Na 2 CO 3 /NaHCO 3 (a) HF is a weak acid and F - is its conjugate base buffer solution (b) HBr is a strong acid not a buffer solution (c) CO 3 2- is a weak base and HCO 3 - is it conjugate acid buffer solution

7 CHM 112 Summer 2007 M. Prushan = 9.20 Calculate the pH of the 0.30 M NH 3 /0.36 M NH 4 Cl buffer system. What is the pH after the addition of 20.0 mL of 0.050 M NaOH to 80.0 mL of the buffer solution? NH 4 + (aq) H + (aq) + NH 3 (aq) pH = pK a + log [NH 3 ] [NH 4 + ] pK a = 9.25 pH = 9.25 + log [0.30] [0.36] = 9.17 NH 4 + (aq) + OH - (aq) H 2 O (l) + NH 3 (aq) start (moles) end (moles) 0.0290.001 0.024 0.0280.00.025 pH = 9.25 + log [0.25] [0.28] [NH 4 + ] = 0.028 0.10 final volume = 80.0 mL + 20.0 mL = 100 mL [NH 3 ] = 0.025 0.10

8 CHM 112 Summer 2007 M. Prushan Maintaining the pH of Blood

9 CHM 112 Summer 2007 M. Prushan Titrations In a titration a solution of accurately known concentration is added gradually added to another solution of unknown concentration until the chemical reaction between the two solutions is complete. Equivalence point – the point at which the reaction is complete Indicator – substance that changes color at (or near) the equivalence point Slowly add base to unknown acid UNTIL The indicator changes color (pink)

10 CHM 112 Summer 2007 M. Prushan Strong Acid-Strong Base Titrations NaOH (aq) + HCl (aq) H 2 O (l) + NaCl (aq) OH - (aq) + H + (aq) H 2 O (l) 0.10 M NaOH added to 25 mL of 0.10 M HCl

11 CHM 112 Summer 2007 M. Prushan

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13 Weak Acid-Strong Base Titrations CH 3 COOH (aq) + NaOH (aq) CH 3 COONa (aq) + H 2 O (l) CH 3 COOH (aq) + OH - (aq) CH 3 COO - (aq) + H 2 O (l) CH 3 COO - (aq) + H 2 O (l) OH - (aq) + CH 3 COOH (aq) At equivalence point (pH > 7):

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16 Solubility Equilibria AgCl (s) Ag + (aq) + Cl - (aq) K sp = [Ag + ][Cl - ]K sp is the solubility product constant MgF 2 (s) Mg 2+ (aq) + 2F - (aq) K sp = [Mg 2+ ][F - ] 2 Ag 2 CO 3 (s) 2Ag + (aq) + CO 3 2 - (aq) K sp = [Ag + ] 2 [CO 3 2 - ] Ca 3 (PO 4 ) 2 (s) 3Ca 2+ (aq) + 2PO 4 3 - (aq) K sp = [Ca 2+ ] 3 [PO 3 3 - ] 2 Dissolution of an ionic solid in aqueous solution: Q = K sp Saturated solution Q < K sp Unsaturated solution No precipitate Q > K sp Supersaturated solution Precipitate will form

17 CHM 112 Summer 2007 M. Prushan

18 Molar solubility (mol/L) is the number of moles of solute dissolved in 1 L of a saturated solution. Solubility (g/L) is the number of grams of solute dissolved in 1 L of a saturated solution.

19 CHM 112 Summer 2007 M. Prushan What is the solubility of silver chloride in g/L ? AgCl (s) Ag + (aq) + Cl - (aq) K sp = [Ag + ][Cl - ] Initial (M) Change (M) Equilibrium (M) 0.00 +s+s +s+s ss K sp = s 2 s = K sp  s = 1.3 x 10 -5 [Ag + ] = 1.3 x 10 -5 M [Cl - ] = 1.3 x 10 -5 M Solubility of AgCl = 1.3 x 10 -5 mol AgCl 1 L soln 143.35 g AgCl 1 mol AgCl x = 1.9 x 10 -3 g/L K sp = 1.6 x 10 -10

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21 If 2.00 mL of 0.200 M NaOH are added to 1.00 L of 0.100 M CaCl 2, will a precipitate form? The ions present in solution are Na +, OH -, Ca 2+, Cl -. Only possible precipitate is Ca(OH) 2 (solubility rules). Is Q > K sp for Ca(OH) 2 ? [Ca 2+ ] 0 = 0.100 M [OH - ] 0 = 4.0 x 10 -4 M K sp = [Ca 2+ ][OH - ] 2 = 8.0 x 10 -6 Q = [Ca 2+ ] 0 [OH - ] 0 2 = 0.10 x (4.0 x 10 -4 ) 2 = 1.6 x 10 -8 Q < K sp No precipitate will form

22 CHM 112 Summer 2007 M. Prushan The Common Ion Effect and Solubility The presence of a common ion decreases the solubility of the salt. What is the molar solubility of AgBr in (a) pure water and (b) 0.0010 M NaBr? AgBr (s) Ag + (aq) + Br - (aq) K sp = 7.7 x 10 -13 s 2 = K sp s = 8.8 x 10 -7 NaBr (s) Na + (aq) + Br - (aq) [Br - ] = 0.0010 M AgBr (s) Ag + (aq) + Br - (aq) [Ag + ] = s [Br - ] = 0.0010 + s  0.0010 K sp = 0.0010 x ss = 7.7 x 10 -10

23 CHM 112 Summer 2007 M. Prushan pH and Solubility The presence of a common ion decreases the solubility. Insoluble bases dissolve in acidic solutions Insoluble acids dissolve in basic solutions Mg(OH) 2 (s) Mg 2+ (aq) + 2OH - (aq) K sp = [Mg 2+ ][OH - ] 2 = 1.2 x 10 -11 K sp = (s)(2s) 2 = 4s 3 4s 3 = 1.2 x 10 -11 s = 1.4 x 10 -4 M [OH - ] = 2s = 2.8 x 10 -4 M pOH = 3.55 pH = 10.45 At pH less than 10.45 Lower [OH - ] OH - (aq) + H + (aq) H 2 O (l) remove Increase solubility of Mg(OH) 2 At pH greater than 10.45Raise [OH - ] add Decrease solubility of Mg(OH) 2


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