Professional Documents
Culture Documents
Chapter 6 Chemical Equilibrium
Chapter 6 Chemical Equilibrium
Chapter 6 Chemical Equilibrium
CHEMICAL EQUILIBRIUM
LEARNING OUTCOME
⚫Kc and Kp
⚫Equilibrium expressions
⚫Conversion of Kc and Kp
Example :
Vaporization of water in a
closed container
!!
The reaction do not stop when
equilibrium is reached.
N2O4 2NO2
(g) gas
colorless (g) color
dark-brown
Characteristic of a system in equilibrium
1 Closed system
aA + bB cC + Dd
Kc = [product] = [C]c[D]d
[reactant] [A]a[B]b
[SO3]2
Kc =
[O2]2[O2]
Unit of Kc :
(mol dm-3)2
(mol dm-3)2(mol dm-3) = dm3 mol-1
• For a reaction, the equilibrium constant for the
forward reaction is Kfwd and the equilibrium
constant for the reverse reaction is Krev.
Kfwd
aA + bB cC + dD
Krev
1
Kfwd = or Kfwd x Krev = 1
Krev
The range of equilibrium constants
small K intermediate K
Very little Significant amount
product
large K of reactant and
Very little product
reactant
[C]c[D]d
K= aA + bB cC + dD
[A]a[B]b
Equilibrium Will
[CH3COO-][H3O+]
Kc = [H2O] = constant
[CH3COOH][H2O]
[CH3COO-][H3O+]
Kc = = Kc′ [H2O]
[CH3COOH]
Example:
CaCO3 (s) CaO (s) + CO2 (g)
Expression of Kc for heterogeneous system
32
CONVERSION OF Kc & Kp
P=
n P n
PV = nRT RT = = M
V RT V
Kp = Kc (RT)Δn(gas)
Kp = Kc(RT)∆n
Kc = [COCl2] 0.14
= = 216 #
[CO][Cl2] 0.012 x 0.054
Kp = Kc(RT)∆n ∆n = 1 – 2 = -1
Solution:
Kp = PNH PH2S = 0.265 x 0.265 = 0.0702
3
Kp = Kc(RT)∆n ∆n = 2 – 0 = 2 T = 295 K
Q= [C]c[D]d Qfwd = 1
[A]a[B]b Qrev
The change in Q during the N2O4-NO2 reaction
At equilibrium
EXERCISE 5
Write the reaction quotient, Qc for the decomposition of
dinitrogen pentoxide
Solution:
Qoverall = Q1 x Q2 x Q3 x …..
Koverall = K1 x K2 x K3 x …..
Example:
Solution:
[NO2]2 (0.55)2
Qc = = = 2.5
[N2O4] (0.12)
46
Calculating Equilibrium Concentrations
ICE
EXERCISE 7
Calculating Kc from Concentration Data
In order to study hydrogen halide decomposition, a
researcher fills an evacuated 2.00-L flask with 0.200 mol of
HI gas and allows the reaction to proceed at 453oC.
Solution:
0.200 mol = 0.100 M
[HI] =
2.00 L
Let x be the amount of [H2] at equilibrium. Then x will
also be the concentration of [I2] and the change in of [HI]
will be the original concentration minus the
stoichiometric amount that reacted, 2x, or 0.078 M.
initial 0.100 0 0
change -2x +x +x
equilibrium 0.100 - 2x x x
(0.500 - x) = 4.8x10-2
CHECK: 0.020/0.500 = 0.04 or 4% percent error
(x)(x) assume x is << 0.010 so
(b) Kc = 8.3x10-4 =
(0.010 - x) that we can drop x in
the denominator
(x)(x)
8.3 x 10-4 = x ≈ 2.9x10-3 M
(0.010)
8.3 x10-6 = x2
(0.010 - x) = 0.0071 M
In one experiment, 1.00 mol of CH4, 1.00 mol of CS2, 2.00 mol
of H2S, and 2.00 mol of H2 are mixed in a 250-mL vessel at
960oC. At this temperature, Kc = 0.036.
[CS2][H2]4 [4.0][8.0]4
Qc = = = 64
[CH4][H2 S]2 [4.0][8.0]2
Remove Remove
Add Add
aA + bB cC + dD
Disturbance +0.075
Change -x -x +x
What happens to
Solution:
a) CO2 is the only gas present. To increase its yield, we
should increase the volume (decrease the pressure).
b) There are more moles of gaseous reactants than
products, so we should decrease the volume (increase
the pressure) to shift the reaction to the right.
EFFECT OF TEMPERATURE
Solution:
(a) CaO(s) + H2O(l) Ca(OH)2(aq) + heat
An increase in temperature will shift the reaction to the left,
decrease [Ca(OH)2], and decrease K.
(b) CaCO3(s) + heat CaO(s) + CO2(g)
The reaction will shift right resulting in an increase in [CO2]
and increase in K.
EFFECT OF CATALYST
A catalyst works by providing an alternative
route that has a lower Ea forward and backward
reaction. The rate of reaction with a catalyst is
much faster and system will reach equilibrium
more quickly
TAKE NOTE!!!!!!
• does not change K
• does not change equilibrium constant
• does not shift the position of an equilibrium
system
SUMMARY OF LE CHATELIER’S PRINCIPLE