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Aqueous Solution and Chemical Equilibria

This document discusses acid-base chemistry and chemical equilibria. It defines acids and bases according to the Bronsted-Lowry theory as proton donors and acceptors. It introduces conjugate acid-base pairs and describes neutralization reactions as proton exchange reactions. It discusses amphiprotic species that can act as both acids and bases, and covers the autoprotolysis of amphiprotic solvents like water. The document also defines chemical equilibrium and explains how equilibrium constants are used to describe different types of acid-base and complexation equilibria through concentration terms. It provides examples of calculating equilibrium concentrations using equilibrium expressions and taking into account chemical species present in excess.

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0% found this document useful (0 votes)
49 views27 pages

Aqueous Solution and Chemical Equilibria

This document discusses acid-base chemistry and chemical equilibria. It defines acids and bases according to the Bronsted-Lowry theory as proton donors and acceptors. It introduces conjugate acid-base pairs and describes neutralization reactions as proton exchange reactions. It discusses amphiprotic species that can act as both acids and bases, and covers the autoprotolysis of amphiprotic solvents like water. The document also defines chemical equilibrium and explains how equilibrium constants are used to describe different types of acid-base and complexation equilibria through concentration terms. It provides examples of calculating equilibrium concentrations using equilibrium expressions and taking into account chemical species present in excess.

Uploaded by

S. Martinez
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Chapter 9

Aqueous solution and


chemical equilibria
Acid and base
• Bronsted-Lowry acid-base concept:
- Acid: proton donor: H2O, HCl, HCOOH
- Base: proton acceptor: NH3, NaOH
- Acid-base reaction is a proton exchange reaction
• Conjugate acid and base:
- A conjugate base of an acid is the product after the acid
give out a proton
- A conjugate acid of a base is the product after the base
accepted a proton
- Example:
acid1 base1 + proton
conjugate base of acid
base2 + proton acid2
conjugate acid of base2
Conjugate acid/base
• Neutralization reaction (a proton exchange reaction):
acid1 + base2 base1 + acid2

• Examples of conjugate acid-base pair


NH3 + H2O NH4+ + OH-
base1 acid2 conjugate conjugate
acid1 base2

H2O + HNO2 H3O+ + NO2-


base1 acid2 conjugate conjugate
acid1 base2
Acid and base
----Amphiprotic species
Amphiprotic species: species possess both acid and base
properties
Examples:
H2PO4- + H3O+ H3PO4 + H2O
base1 acid2 acid1 base2

H2PO4- + OH- HPO42- + H2O


acid1 base2 base1 acid2

NH2CH2COOH + H3O+ NH3+CH2COOH + H2O


base1 acid2 acid1 base2

NH2CH2COOH + OH- NH3CH2COO- + H2O


acid1 base2 base1 acid2

NH2CH2COOH NH3+CH2COO- (zwitterion)


base1 acid2 acid1 base2
Amphiprotic solvent and autoprotolysis
• Amphiprotic solvent: a solvent acts either as an acid or as a base.
• Examples: H2O, NH3, HCOOH, CH3OH, C2H5OH.
• Autoprotolysis: a process solvents undergo self-ionization to
form a pair of ionic species.
• Examples
base1 acid2 acid1 base2
H2O + H2O H3O+ + OH-
NH3 + NH3 NH4+ + NH2-
CH3OH + CH3OH CH3OH2+ + CH3O-
HCOOH + HCOOH HCOOH2+ + HCOO-
Chemical equilibrium

• Equilibrium state: the rate of reactants react to generate


products equals the rate of the products react to generate
reactants. (equilibrium, not static. No change macroscopically, but change microscopically)

• Expression:
reactant1 + reactant2 product1 + product2
• Equilibrium position is decided by the thermochemical
property of the reaction system, independent of the route
by which the equilibrium is reached (The 1st thermodynamic
law).
Equilibrium constant expression
• For a general chemical reaction:
wW + xX yY + zZ
• Equilibrium constant:
[Y]y[Z]z
K= (9-1)
[W]w[X]x
• [X] indicates the equilibrium concentration of component X.

• If a reactant is a pure liquid, pure solid or the solvent


present in excess, no term for that species appears in
the equilibrium constant expression.
[Y]y
K= (9-2) (Z is a solid reactant)
[W]w[X]x
Type of equilibrium constants in
analytical chemistry
Type of Name&symbol Typical example Equilibrium
equilibrium of equilibrium constant
constant expression
Dissociation of Ion-product
water constant, Kw 2H2O H3O+ + OH- Kw = [H3O+][OH-]

Dissolving of Solubility
slightly soluble product, Ksp BaSO4(s) Ba2+ + SO42- Ksp = [Ba2+][SO42-]
substance

Dissociation of Dissociation
[H3O+][Ac-]
weak acid or constant, Ka or HAc + H2O H3O+ + Ac- Ka = [HAc]
base Kb

Complex Formation
[Ni(CN)42-]
formation constant, β Ni2+ + 4CN- Ni(CN)42- β = [Ni2+][CN-]4
Type of equilibrium constants in
analytical chemistry
Type of Name&symbol Typical example Equilibrium
equilibrium of equilibrium constant
constant expression
Oxidation/reduction Kredox MnO4- + 5Fe2+ + 8H+ Kredox =
equilibrium Mn2+ + 5Fe3+ + 4H2O [Mn2+][Fe3+]5
[MnO4-][Fe2+]5[H+]8
Distribution of a
solute between Kd I2(aq) I2(org) Kd = [I2]org/[I2]aq
immiscible solvents
Stepwise formation constant for
complexation reactions
• Stepwise formation of complexes
[Ni(CN)+]
Ni2+ + CN- Ni(CN)+ K1 =
[Ni2+][CN-]
[Ni(CN)2]
Ni(CN)+ + CN- Ni(CN)2 K2 =
[Ni(CN)+][CN-]

Ni(CN)2 + CN- NI(CN)3- [Ni(CN)3-]


K3 =
[Ni(CN)2][CN-]
Ni(CN)3- + CN- Ni(CN)42- [Ni(CN)42-]
K4 =
[Ni(CN)3-][CN-]
Overall formation constant of
complexes
• Overall formation of complexes
[Ni(CN)2]
Ni2+ + 2CN- Ni(CN)2 β2 =K1 K2 =
[Ni2+][CN-]2
[Ni(CN)3]
Ni2+ + 3CN- Ni(CN)2 β3 =K1 K2 K3 =
[Ni2+][CN-]3
[Ni(CN)4]
Ni2+ + 4CN- NI(CN)4- β4 =K1 K2 K3 K4=
[Ni2+][CN-]4
Application of equilibrium constant
in calculations
• “If a reactant is a pure liquid, pure solid or the solvent
present in excess, no term for that species appears in
the equilibrium constant expression”

Take water as an example: water molar concentration in an


dilute aqueous solution is:
1000g/L = 55.6 M
18 g
In a pure water solution, the dissociation reaction will generate 1.0 x 10-7
M H3O+ ions and 1.0 x 10-7 M OH- ions. If we add HCl to the solution to
make a 0.1 M HCl solution, Suppose all the OH- ions in water reacted with
H3O+ ions, then water concentration will increase 1.0 x 10-7 M. Therefore,
the change of water concentration is negligible.
Q Do it your self
1. What is the H3O+ concentration in a 0.001 M
NaOH solution. (Kw = 1.00 x 10-14), and what is
the OH- concentration in the solution?
2. Suppose the Ksp for Ba(IO3)2 is 1.57 x 10-9.
What is the Ba2+ concentration and IO3-
concentration in a solution in equilibrium with
solid Ba(IO3)2 (a saturated Ba(IO3)2 solution).
3. if 2.00 x 10-2 M Ba2+ is added to the Ba(IO3)2
saturated solution, then, what is the
concentration of Ba2+ and IO3- in the solution.
(Common ion effect).
Dissociation constants for
conjugate acid/base pair
• Take NH4+/NH3 conjugate acid/base pair as an example:
- Dissociation of NH4+ [NH3][H3O+]
NH4+ + H2O NH3 + H3O+ Ka =
[NH4+]
- Dissociation of NH3: [NH4+][OH-]
NH3 + H2O NH4+ + OH- Kb =
[NH3]

[NH3][H3O+] [NH4+][OH-]
KaKb = x = [H3O+][OH-] = Kw
[NH4+] [NH3]

Kw = KaKb (9-3)
Q Do it yourself
• Calculate the dissociation constant of conjugate acid/base

Acid Ka Base Kb

NH4+ ? NH3 1.75 x 10-5

C6H5COOH 6.28 x 10-5 C6H5COO- ?

CH3COOH 1.75 x 10-5 CH3COO- ?

ClCH2COOH 1.36 x 10-3 ClCH2COO- ?


Hydronium ion concentration of
solutions of weak acids
• Dissociation reactions in a weak acid solution
HA + H2O H3O+ + A- [A-][H3O+]
Ka = (9-4)
[HA]
2H2O H3O+ + OH- Kw = [H3O+][OH-]
• Water dissociation is negligible in such a solution
(common ion effect)

• Suppose the analytical concentration of the weak acid in the


solution is CHA
• What we need to know if we want to calculate [H3O+]
using the dissociation constant equation?
[A-][H3O+]
Ka = (9-4)
[HA]
Hydronium ion concentration of
solutions of weak acids
[A-][H3O+]
• From the dissociation reaction: Ka =
[HA]
[A-] = [H3O+]
CHA = [A-] + [HA] = [H3O+] + [HA]
[HA] = CHA – [H3O+]
• Re-write dissociation constant expression:
[A-][H3O+] [H3O+]2
Ka = = (9-5)
[HA] CHA – [H3O+]
Resulted in an equation:
[H3O+]2 + Ka[H3O+] – KaCHA = 0 (9-6)
Hydronium ion concentration of
solutions of weak acids
• Solution of equation (9-6):

-Ka + Ka2 + 4KaCHA


[H3O+] = (9-7)
2
• We are dealing with a WEAK acid, it is supposed the
dissociation is very limited. Therefore, we can assume
[H3O+] << CHA and CHA – [H3O+] = CHA

• Rewrite equation (9-5)


[H3O+]2
Ka = (9-8)
CHA

[H3O+] = KaCHA (9-9)


Q Do it yourself
Acetic acid, CH3COOH, is an essential ingredient of
commercial vinegar, which gives the flavor you tasted. A
commercial vinegar usually have 5.00% (w/w) acetic acid.
The density of vinegar is 1.01 g/mL (http://www.apple-cider-vinegar-
benefits.com/properties-of-vinegar.html#phv). Suppose there is no
other ingredient contribute to [H3O+] in the vinegar, calculate
[H3O+] concentration in the vinegar (Acetic acid, MCH3COOH =
60.0 g; Ka = 1.75 x 10-5)
Buffer solutions
• Definition: A buffer solution resist the changes in pH with
dilution or with addition of acid or base.
• Composition: buffer solutions consist of conjugate acid/base
pairs.
• Examples: NH3/NH4Cl, NaH2PO4/Na2HPO4, HOAc/NaOAc
Buffer solution calculation
-----What is the pH value of a buffer solution
• Dissociation reactions in a buffer solution consists of a
conjugate acid/base pair: HA/NaA
- +]
[A ][H O
HA + H2O H3O+ + A- Ka =
3 (9-4)
[HA]
A- + H2O HA + OH- [HA][OH-] Kw
Kb = = (9-10)
[A-] Ka
• From these reactions:
[HA] = CHA – [H3O+] + [OH-] = CHA (9-11)
[A-] = CNaA + [H3O+] - [OH-] = CNaA (9-12)

• Replace [HA] and [A-] in equation 9-4 with the value


expressed in equation 9-11 and 9-12
+ CHA (9-13)
[H3O ] = Ka
CNaA
pH = pKa - logCHA + logCNaA (9-14)
Properties of buffer solutions
CHA
[H3O+] = Ka
CNaA
1. Buffer the pH change in dilution.
2. Buffer pH change in case acid or base of limited
quantity was added to the solution
• Example: a 400 mL buffer solution having 0.200 M
NH3 and 0.300 M NH4Cl. Calculate the pH change
after 100 mL of 0.0500 M NaOH solution is added to
the buffer solution. (NH3, Kb = 1.75 x 10-5)
Solution:
- Before addition of NaOH solution
pOH = pKb - logCNH3 + logCNH4Cl = 4.75 + 0.699 - 0.522
= 4.93
pH = 14.00 – 4.93 = 9.07
Properties of buffer solution
• After adding NaOH solution
NH4+ + OH- NH3 + H2O
400x0.300 – 100x0.0500
CNH4+ = = 0.230 M
400 + 100
400x0.200 + 100x0.0500
CNH3 = = 0.170 M
400 + 100
pOH = pKb - logCNH3 + logCNH4Cl = 4.75 + 0.769 – 0.638
= 4.88
pH = 14.00 – 4.88 = 9.12
∆pH = 9.12 – 9.07 = 0.05

• If without buffer, the pH change will be from pH = 7 (pure


water) to pH = 12 (0.01 M NaOH). ∆pH = 5.
The composition of buffer solutions
as a function of pH, α values
• α value: the relative equilibrium concentration of the two
components of a conjugate acid/base pair.
• A buffer solution consists of HA and NaA. The α values
for HA and NaA can be calculated with follow equation:
[H3O+]
αHA =
[H3O+] + Ka

[H3O+] + Ka
αNaA =
[H3O+]

In a solution with pH = pKa, αHA = αNaA. Most of the transition


between αHA and αNaA occurs within + 1 pH unit around pH =
pKa.
Buffer capacity
• Definition: buffer capacity is the number of moles of a
strong acid or base that causes 1.00 L of a buffer solution to
undergoing a 1.00 unit change in pH.

dCb dCa
β=
dpH = - dpH

• The bigger the β value, the stronger the buffer solution to


resist a change of pH value caused by the addition of an
acid or base.
How to select and prepare a buffer solution

• Consider what pH range you want the


solution to keep, choose the central pH
value as close as possible to pKa
• Choose appropriate buffer capacity.
• The recipes of many commonly used
buffer solutions can be founded in
chemical handbooks (e.g. J. A. Dean, Analytical
chemistry Handbook, New York, McGraw-Hill, 1995).
Q Question
• What is the components buffered the
potential vigorous pH change in river and
lake water caused by acid rain?

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