1. CHAPTER 16: ACID BASE EQUILIBRIA Wasilla High School 2015 - 2016

2. ARRHENIUS DEFINITION An acid is a substance that, when dissolved in water, increases the concentration of hydrogen ions (H + ) An acid is a substance that, when dissolved in water, increases the concentration of hydrogen ions (H + ) HCl HCl H 2 SO 4 H 2 SO 4 A base is a substance that, when dissolved in water, increases the concentration of hydroxide ions (OH - ) A base is a substance that, when dissolved in water, increases the concentration of hydroxide ions (OH - ) NaOH NaOH KOH KOH

3. BRØNSTED–LOWRY DEFINITION An acid is a proton donor. An acid is a proton donor. A Brønsted–Lowry acid must have a removable (acidic) proton. A Brønsted–Lowry acid must have a removable (acidic) proton. A base is a proton acceptor. A base is a proton acceptor. A Brønsted–Lowry base must have a pair of nonbonding electrons. A Brønsted–Lowry base must have a pair of nonbonding electrons. If it can be either it’s amphiprotic If it can be either it’s amphiprotic H 2 O can either gain or lose H + H 2 O can either gain or lose H +

4. CONJUGATE ACIDS AND BASES Reactions between acids and bases always yield their conjugate bases and acids. Reactions between acids and bases always yield their conjugate bases and acids.

5. WHAT HAPPENS WHEN AN ACID DISSOLVES IN WATER? Water acts as a Brønsted–Lowry base and abstracts a proton (H + ) from the acid. Water acts as a Brønsted–Lowry base and abstracts a proton (H + ) from the acid. As a result, the conjugate base of the acid and a hydronium ion are formed. As a result, the conjugate base of the acid and a hydronium ion are formed.

6. ACID AND BASE STRENGTH Strong acids are completely dissociated in water. Their conjugate bases are quite weak. Weak acids only dissociate partially in water. Their conjugate bases are weak bases. Substances with negligible acidity do not dissociate in water. Their conjugate bases are exceedingly strong.

7. ACID AND BASE STRENGTH In any acid–base reaction, the equilibrium will favor the reaction that moves the proton to the stronger base. In any acid–base reaction, the equilibrium will favor the reaction that moves the proton to the stronger base. HCl (aq) + H 2 O (l)  H 3 O + (aq) + Cl  (aq) H 2 O is a much stronger base than Cl , so the equilibrium lies so far to the right that K is not measured (K >> 1). CH 3 CO 2 H (aq) + H 2 O (l) H 3 O + (aq) + CH 3 CO 2  (aq) Acetate is a stronger base than H 2 O, so the equilibrium favors the left side (K < 1).

8. AUTOIONIZATION OF WATER As we have seen, water is amphoteric. As we have seen, water is amphoteric. In pure water, a few molecules act as bases and a few act as acids. In pure water, a few molecules act as bases and a few act as acids. This is referred to as autoionization. This is referred to as autoionization.

9. ION PRODUCT CONSTANT The equilibrium expression for this process is The equilibrium expression for this process is K c = [H 3 O + ] [OH  ] Or K c = [H + ] [OH  ] This special equilibrium constant is referred to as the ion product constant for water, K w. This special equilibrium constant is referred to as the ion product constant for water, K w. At 25  C, K w = 1.0  10  14 At 25  C, K w = 1.0  10  14

10. PH pH is defined as the negative base-10 logarithm of the concentration of hydronium ion: pH =  log [H 3 O + ] Or pH =  log [H + ]

11. PH In pure water, In pure water, K w = [H 3 O + ] [OH  ] = 1.0  10  14 Since in pure water, [H 3 O + ] = [OH  ], Since in pure water, [H 3 O + ] = [OH  ], [H 3 O + ] =  1.0  10  14 = 1.0  10  7

12. PH Therefore, in pure water, Therefore, in pure water, pH =  log (1.0  10  7 ) = 7.00 An acid has a higher [H 3 O + ] than pure water, so its pH is <7. An acid has a higher [H 3 O + ] than pure water, so its pH is <7. A base has a lower [H 3 O + ] than pure water, so its pH is >7. A base has a lower [H 3 O + ] than pure water, so its pH is >7.

13. OTHER “P” SCALES The “p” in pH tells us to take the negative base-10 logarithm of the quantity (in this case, hydronium ions). The “p” in pH tells us to take the negative base-10 logarithm of the quantity (in this case, hydronium ions). Some similar examples are Some similar examples are pOH:  log [OH  ] pOH:  log [OH  ] pK w :  log K w pK w :  log K w

14. WATCH THIS! Because [H 3 O + ] [OH  ] = K w = 1.0  10  14 we know that  log [H 3 O + ] +  log [OH  ] =  log K w = 14.00  log [H 3 O + ] +  log [OH  ] =  log K w = 14.00 or, in other words, pH + pOH = pK w = 14.00

15. STRONG ACIDS You will recall that the seven strong acids are HCl, HBr, HI, HNO 3, H 2 SO 4, HClO 3, and HClO 4. You will recall that the seven strong acids are HCl, HBr, HI, HNO 3, H 2 SO 4, HClO 3, and HClO 4. These are, by definition, strong electrolytes and exist totally as ions in aqueous solution. These are, by definition, strong electrolytes and exist totally as ions in aqueous solution. For the monoprotic strong acids, For the monoprotic strong acids, [H + ]=[H 3 O + ] = [acid].

16. STRONG BASES Strong bases are the soluble hydroxides, which are the alkali metal and heavier alkaline earth metal hydroxides (Ca 2+, Sr 2+, and Ba 2+ ). Strong bases are the soluble hydroxides, which are the alkali metal and heavier alkaline earth metal hydroxides (Ca 2+, Sr 2+, and Ba 2+ ). Again, these substances dissociate completely in aqueous solution. Again, these substances dissociate completely in aqueous solution. © 2012 Pearson Education, Inc.

17. DISSOCIATION CONSTANTS For a generalized acid dissociation, For a generalized acid dissociation, the equilibrium expression would be This equilibrium constant is called the acid- dissociation constant, K a. This equilibrium constant is called the acid- dissociation constant, K a. [H 3 O + ] [A  ] [HA] K c = HA (aq) + H 2 O (l) A  (aq) + H 3 O + (aq)

18. DISSOCIATION CONSTANTS The greater the value of K a, the stronger is the acid.

19. CALCULATING K A FROM THE PH The pH of a 0.10 M solution of formic acid, HCOOH, at 25  C is 2.38. Calculate K a for formic acid at this temperature. We know that We know that [H 3 O + ] [HCOO  ] [HCOOH] K a =

20. CALCULATING K A FROM THE PH The pH of a 0.10 M solution of formic acid, HCOOH, at 25  C is 2.38. Calculate K a for formic acid at this temperature. To calculate K a, we need the equilibrium concentrations of all three things. We can find [H 3 O + ], which is the same as [HCOO  ], from the pH.

21. CALCULATING K A FROM THE PH pH=  log [H 3 O + ] pH=  log [H 3 O + ] 2.38=  log [H 3 O + ] 2.38=  log [H 3 O + ]  2.38= log [H 3 O + ]  2.38= log [H 3 O + ] 10  2.38 = 10 log [H 3 O + ] = [H 3 O + ] 10  2.38 = 10 log [H 3 O + ] = [H 3 O + ] 4.2  10  3 = [H 3 O + ] = [HCOO  ]

22. CALCULATING K A FROM PH Now we can set up a table… [HCOOH], M[H 3 O + ], M[HCOO  ], M Initially0.1000 Change At equilibrium

23. CALCULATING K A FROM PH Now we can set up a table… [HCOOH], M[H 3 O + ], M[HCOO  ], M Initially0.1000 Change  4.2  10  3 +4.2  10  3 At equilibrium

24. CALCULATING K A FROM PH Now we can set up a table… [HCOOH], M[H 3 O + ], M[HCOO  ], M Initially0.1000 Change  4.2  10  3 +4.2  10  3 At equilibrium 0.10  4.2  10  3 = 0.0958 = 0.10 4.2  10  3 © 2012 Pearson Education, Inc.

25. CALCULATING K A FROM PH [4.2  10  3 ] [0.10] K a = = 1.8  10  4

26. CALCULATING PERCENT IONIZATION Percent ionization =  100 Percent ionization =  100 In this example, In this example, [H 3 O + ] eq = 4.2  10  3 M [HCOOH] initial = 0.10 M [HCOOH] initial = 0.10 M [H 3 O + ] eq [HA] initial Percent ionization =  100 4.2  10  3 0.10 = 4.2%

27. CALCULATING PH FROM K A Calculate the pH of a 0.30 M solution of acetic acid, HC 2 H 3 O 2, at 25  C. HC 2 H 3 O 2 (aq) + H 2 O (l) H 3 O + (aq) + C 2 H 3 O 2  (aq) HC 2 H 3 O 2 (aq) + H 2 O (l) H 3 O + (aq) + C 2 H 3 O 2  (aq) K a for acetic acid at 25  C is 1.8  10  5. K a for acetic acid at 25  C is 1.8  10  5.

28. CALCULATING PH FROM K A The equilibrium constant expression is [H 3 O + ] [C 2 H 3 O 2  ] [HC 2 H 3 O 2 ] K a =

29. CALCULATING PH FROM K A We next set up a table… [C 2 H 3 O 2 ], M[H 3 O + ], M[C 2 H 3 O 2  ], M Initially0.3000 Change At equilibrium We are assuming that x will be very small compared to 0.30 and can, therefore, be ignored.

30. CALCULATING PH FROM K A We next set up a table… [C 2 H 3 O 2 ], M[H 3 O + ], M[C 2 H 3 O 2  ], M Initially0.3000 Change xx +x+x+x+x At equilibrium We are assuming that x will be very small compared to 0.30 and can, therefore, be ignored.

31. CALCULATING PH FROM K A We next set up a table… [C 2 H 3 O 2 ], M[H 3 O + ], M[C 2 H 3 O 2  ], M Initially0.3000 Change xx +x+x+x+x At equilibrium 0.30  x  0.30 xx We are assuming that x will be very small compared to 0.30 and can, therefore, be ignored.

32. CALCULATING PH FROM K A Now, (x) 2 (0.30) 1.8  10  5 = (1.8  10  5 ) (0.30) = x 2 5.4  10  6 = x 2 2.3  10  3 = x

33. CALCULATING PH FROM K A pH =  log [H 3 O + ] pH =  log (2.3  10  3 ) pH = 2.64

34. POLYPROTIC ACIDS Polyprotic acids have more than one acidic proton. Polyprotic acids have more than one acidic proton. If the difference between the K a for the first dissociation and subsequent K a values is 10 3 or more, the pH generally depends only on the first dissociation.

35. WEAK BASES Bases react with water to produce hydroxide ion.

36. WEAK BASES The equilibrium constant expression for this reaction is [HB] [OH  ] [B  ] K b = where K b is the base-dissociation constant.

37. WEAK BASES K b can be used to find [OH  ] and, through it, pH.

38. PH OF BASIC SOLUTIONS What is the pH of a 0.15 M solution of NH 3 ? [NH 4 + ] [OH  ] [NH 3 ] K b = = 1.8  10  5 NH 3 (aq) + H 2 O (l) NH 4 + (aq) + OH  (aq)

39. PH OF BASIC SOLUTIONS Tabulate the data. [NH 3 ], M[NH 4 + ], M[OH  ], M Initially0.1500 At equilibrium

40. PH OF BASIC SOLUTIONS Tabulate the data. [NH 3 ], M[NH 4 + ], M[OH  ], M Initially0.1500 At equilibrium 0.15  x  0.15 xx

41. PH OF BASIC SOLUTIONS (1.8  10  5 ) (0.15) = x 2 2.7  10  6 = x 2 1.6  10  3 = x 2 (x) 2 (0.15) 1.8  10  5 =

42. PH OF BASIC SOLUTIONS Therefore, [OH  ] = 1.6  10  3 M [OH  ] = 1.6  10  3 M pOH =  log (1.6  10  3 ) pOH = 2.80 pH = 14.00  2.80 pH = 14.00  2.80 pH = 11.20

43. K A AND K B K a and K b are related in this way: K a  K b = K w Therefore, if you know one of them, you can calculate the other.

44. REACTIONS OF ANIONS WITH WATER Anions are bases. Anions are bases. As such, they can react with water in a hydrolysis reaction to form OH  and the conjugate acid: As such, they can react with water in a hydrolysis reaction to form OH  and the conjugate acid: X  (aq) + H 2 O (l) HX (aq) + OH  (aq)

45. REACTIONS OF CATIONS WITH WATER Cations with acidic protons (like NH 4 + ) will lower the pH of a solution. Most metal cations that are hydrated in solution also lower the pH of the solution.

46. REACTIONS OF CATIONS WITH WATER Attraction between nonbonding electrons on oxygen and the metal causes a shift of the electron density in water. This makes the O–H bond more polar and the water more acidic.

47. REACTIONS OF CATIONS WITH WATER Greater charge and smaller size make a cation more acidic.

48. EFFECT OF CATIONS AND ANIONS 1.An anion that is the conjugate base of a strong acid will not affect the pH. 2.An anion that is the conjugate base of a weak acid will increase the pH. 3.A cation that is the conjugate acid of a weak base will decrease the pH.

49. EFFECT OF CATIONS AND ANIONS 4.Cations of the strong Arrhenius bases will not affect the pH. 5.Other metal ions will cause a decrease in pH. 6.When a solution contains both a weak acid and a weak base, the affect on pH depends on the K a and K b values.

50. FACTORS AFFECTING ACID STRENGTH The more polar the H– X bond and/or the weaker the H–X bond, the more acidic the compound. The more polar the H– X bond and/or the weaker the H–X bond, the more acidic the compound. So acidity increases from left to right across a row and from top to bottom down a group. So acidity increases from left to right across a row and from top to bottom down a group.

51. FACTORS AFFECTING ACID STRENGTH In oxyacids, in which an –OH is bonded to another atom, Y, the more electronegative Y is, the more acidic the acid.

52. FACTORS AFFECTING ACID STRENGTH For a series of oxyacids, acidity increases with the number of oxygens.

53. FACTORS AFFECTING ACID STRENGTH Resonance in the conjugate bases of carboxylic acids stabilizes the base and makes the conjugate acid more acidic.