Aqueous Equilibria - PowerPoint PPT Presentation

1 / 32
About This Presentation
Title:

Aqueous Equilibria

Description:

Aqueous Equilibria Chapter 16 pH The pH of aqueous solutions not only blood plasma, but seawater, detergents, sap and reaction mixtures is controlled, by the transfer ... – PowerPoint PPT presentation

Number of Views:63
Avg rating:3.0/5.0
Slides: 33
Provided by: etsuEduco
Category:

less

Transcript and Presenter's Notes

Title: Aqueous Equilibria


1
Aqueous Equilibria
  • Chapter 16

2
pH
  • The pH of aqueous solutions not only blood
    plasma, but seawater, detergents, sap and
    reaction mixtures is controlled, by the transfer
    of protons between ions and water molecules.

3
Ions as acids and bases
  • Any cation that is the conjugate acid of a weak
    base functions as an acid and lowers the pH of
    the solution. Ammonium ion the conjugate acid of
    weak base ammonia, is an acid.
  • NH4 (aq) H2O(l)? H3O(aq) NH3(aq)
  • Small highly charged metal cations that can act
    as Lewis acids in water, such as Al3 and Ti3
    also produce acidic solutions, even though the
    cations dont have any protons to donate. The
    protons come from the water molecules that
    hydrate the ions in solution.

4
  • Salts that contain the conjugate acids of weak
    bases produce acidic aqueous solutions so do
    salts that contain small, highly charged metal
    cations. Salts that contain the conjugate bases
    of weak acids produce basic aqueous solutions.

5
pH of a salt solution
  • Aquoeus solutions of salts with acidic cations
    have a pH lower than 7 salts with basic anions
    produce a pH higher than 7 in aqueous solutions.

6
Class Practice
  • Estimate the pH of 0.15M
  • Ca(CH3COO)2(aq).

7
pH of mixed solutions
  • The pH of a solution of a weak acid increases
    when a salt containing its conjugate base is
    added. The pH of a solution of a weak base
    decreases when a salt containing its conjugate
    acid is added.

8
Class Practice
  • Calculate the pH of a solution that is 0.500 M
    HNO2(aq) and 0.100M KNO2(aq)
  • Ka4.3x10-4 for HNO2

9
Titrations
  • Strong acid strong base titrations

10
  • Strong base and strong acid

11
  • In the titration of a strong acid with a strong
    base (or a strong base with a strong acid), the
    pH increases (or decreases) slowly initially,
    increases (or decreases) rapidly through pH7 at
    the stoichiometric point, and then increases (or
    decreases) slowly again.

12
Class Practice
  • Suppose we carry out a titration in which 0.34M
    HCl (aq) is the titrant and the analyte initially
    consists of 25 ml of 0.25M NaOH (aq). What is the
    pH of the analyte solution after the addition of
    5 ml of titrant?

13
Calculating the pH at the stochiometric point of
the titration of weak acid with strong base
  • Calculate the pH of the solution resulting when 5
    ml of 0.150 M NaOH (aq) is added to 25 ml of
    0.100M HCOOH (aq) . Use Ka1.8x10-4 for HCOOH
    (aq).

14
Buffer solutions
  • Solutions that resist the change in pH when small
    amounts of strong acids or base are added are
    called as buffers.

15
Acid Buffer
  • An acid buffer solution consists of a weak acid
    and its conjugate base it has pHlt7.
  • CH3COOH (aq) H2O(l)?H3O(aq) CH3CO2- (aq)
  • Acid Buffer action The weak acid transfers
    protons to the OH- ions from added strong base.
  • The conjugate base of the weak acid accepts
    protons from the H3O ions supplied by a strong
    acid.

16
Base Buffer
  • A base buffer solution consists of a weak base
    and its conjugate acid it has pH gt7.
  • NH3(aq) H2O(l)?NH4 (aq) OH- (aq)
  • Base Buffer action The weak base accepts protons
    from the H3O ions supplied by a strong acid.
  • The conjugate acid of the weak base transfers
    protons to the OH- ions from added strong base.

17
Calculate the pH of a buffer solution
  • For a solution containing a weak acid HA and a
    salt that provides the conjugate base anion, A- ,
    the proton transfer equilibrium is
  • HA(aq) H2O(l)?H3O (aq) A- (aq)
  • KaH3O A-/HA
  • Rearranging the equation
  • 1/H3O 1/Ka xA-/HA

18
  • Taking logarithm of both sides
  • log1/H3O log1/ Ka logA-/HA
  • -logH3O -logKa logA-/HA
  • That is pH pka logA-/HA
  • pH pKa log (baseinitial/acidinitial)
  • This relation is called the Henderson Hassel
    balch equation.

19
Class Practice
  • Calculate the pH of a buffer solution that is
    0.40 M NaCH3CO2 (aq) and 0.80M CH3COOH(aq) at
    25C.
  • Calculate the ratio of the molarities of CO32-
    and HCO3- ions required to achieve buffering at
    pH 9.50. The pka of H2CO3 is 10.25.

20
Solubility product
  • The solubility product is the equilibrium
    constant for the equilibrium between an un
    dissolved salt and its ions in a saturated
    solution.

21
Class Practice
  • The molar solubility of silver chromate Ag2CrO4
    is 6.5x10-5 mol/L. determine the value of Ksp.
  • The Ksp for lead(II)iodide in water is 1.4x10-8 .
    Estimate its molar solubility.

22
The common ion effect
  • The common-ion effect is a term used to describe
    the effect on a solution of two dissolved solutes
    that contain the same ion.The presence of a
    common ion suppresses the ionization of a weak
    acid or a weak base.

23
  • If both sodium acetate and acetic acid are
    dissolved in the same solution they both
    dissociate and ionize to produce acetate ions.
    Sodium acetate is a strong electrolyte so it
    dissociates completely in solution. Acetic acid
    is a weak acid so it only ionizes slightly.
  • NaC2H3O2(s) ? Na(aq) C2H3O2-(aq) HC2H3O2(l) ?
    H(aq) C2H3O2-(aq)

24
  • According to Le Chatelier's principle, the
    addition of acetate ions from sodium acetate will
    suppress the ionization of acetic acid and shift
    its equilibrium to the left. This will decrease
    the hydrogen ion concentration and thus the
    common-ion solution will be less acidic than a
    solution containing only acetic acid.

25
Class Practice
  • What is the approximate molar solubility of
    silver chloride in 0.10M NaCl (aq)?

26
Predicting precipitation
  • In the Ksp expression the right hand side of the
    expression is known as the "ion product". At
    saturation when the ions in solution are in
    equilibrium with the solid slightly soluble salt,
    the ion product is equal to a fixed value called
    the solubility product constant
  • Ksp ion product

27
  • Two further cases exist
  • ion product lt Ksp
  • ion product gt Ksp
  • If the ion product lt Ksp then no precipitation
    will occur even though the salt may be insoluble
    according to the solubility rules. If, on the
    other hand, the ion product gt Ksp the ion
    concentration will be large enough for
    precipitation to occur

28
  • The concentration of Calcium ion in blood plasma
    is 0.0025 M. If the concentration of Oxalate ion
    is 1 X 10-8 M. Will Calcium Oxalate, CaC2O4
    precipitate? Ksp 2.3 X 10-9.

29
  • Write the slightly soluble salt equilibria.
    CaC2O4 Ca2 C2O4-2
  • Write the ion product ion product Ca2
    C2O4-2
  • Identify the given ion concentrations
  • Ca2 .0025 2.5 X 10-3 M
  • C2O4-2 1 X 10-8 M
  • Plug in the given ion concentrations into the ion
    product equation

30
  • ion product Ca2 C2O4-2 (2.5 X 10-3) ( 1
    X 10-8)
  • ion product 2.5 X 10-11
  • Compare the ion product value with Ksp value and
    make a conclusion. Since the ion product value
    (2.5 X 10-11) is less than the Ksp (2.3 X 10-9)
    we have to conclude that no precipitation will
    take place.

31
Class Practice
  • Lead II Chromate, PbCrO4, is used in yellow paint
    pigment("chrome yellow"). When the solution is
    5.0 X 10-4 M in Pb2 ion and 5.0 X 10-5 M in
    Chromate ion. Would you expect some of the Lead
    Chromate to precipitate. Ksp PbCrO4 1.8 X
    10-14.

32
Homework
  • Page 744
  • 16.22 all
  • 16.30 all
  • 16.55 all
  • 16.85
Write a Comment
User Comments (0)
About PowerShow.com