chapter 13 chemical equilibrium - kfupm 102-ch 13... · 2009. 3. 10. · chapter 13 chemical...
TRANSCRIPT
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Chapter 13Chemical Equilibrium
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Topics
What is meant by equilibrium?Equilibrium conditions Equilibrium constant and law of mass actionEquilibrium expressions involving pressuresHeterogeneous equilibriaApplications of equilibrium constant and solving equilibria problemsLe Chatelier’s Principle
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Introduction Chemical Equilibrium
The state where the concentrations of all reactants and products remain constant with time.
Equilibrium is not static, but is a highly dynamic situation.
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13.1 The Equilibrium Conditions Reactions are reversible
A + B C + D ( forward)C + D A + B (reverse)Initially there is only A and B so only the forward reaction is possibleAs C and D build up, the reverse reaction speeds up while the forward reaction slows down.Eventually the rates are equal
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Rea
ctio
n R
ate
Time
Forward Reaction
Reverse reaction
EquilibriumDynamic?
Rate forwards = Rate reverse
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Equilibrium conditionsRates of forward and reverse reactions are equal if temperature remains constantConcentrations are not equal.Factors affecting the equilibrium position of a reaction:
initial concentrations; relative energies of reactants and products;Relative degree of organization of reactants and products(Nature tends to achieve minimum energy and maximum disorder
The concentrations of reactants or products do not change at equilibrium.
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13.2 The equilibrium constantLaw of Mass Action
For any reaction jA + kB lC + mD
[C]l[D]m PRODUCTSpower
[A]j[B]k REACTANTSpower
K is called the equilibrium constant.
is how a reversible reaction is identified
K =
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Comments on Law of mass actionK is constant regardless of the amounts of materials mixed initiallyEquilibrium concentrations will notalways be the same but K is the same
Each set of equilibrium concentrations in an equilibrium system is called equilibrium positionThere is only one K value for a given system but infinite number of equilibrium positionsThe law of mass action applies to solution and gaseous equilibria
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Changing the chemical equation of an equilibrium system: Reciprocal rule
If we write the reaction in reverse.lC + mD jA + kBThen the new equilibrium constant is
K’ = K1
[D][C] [B][A]
ml
kj
= Reciprocal rule
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Multiplying the equation by a coefficient:Coefficient Rule
If we multiply the equation by a constantnjA + nkB nlC + nmDThen the equilibrium constant is
K’ = [C]nl[D]nm= ([C] l[D]m)n
= Kn
[A]nj[B]nk ([A]j[B]k)n
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Rules of Multiple EqulibriaReaction 3 = Reaction 1 + Reaction 2
SO2(g) + 1/2O2 SO3(g); K1 = 2.2NO2(g) NO(g) + 1/2O2(g); K2 = 4.0
SO2(g) +NO2(g) SO3(g) + NO (g);
K3=2.2 X4.0 = 8.8
22
3
NOSO
NOSO
PPXPP
K3 = K1XK2
K3 = = K1XK2
K (Reaction 3) =K (reaction 1) X K (reaction 2)
2122
31 l
OSO
SO
XPPpK =
2
2/12
2NO
ONO
PXPPK =
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Notes on Equilibrium Expressions
The Equilibrium Expression for a reaction is the reciprocalreciprocal of that for the reaction written in reversereverse.When the equation for a reaction is multiplied by n, the equilib expression changes as follows: (Equilib Expression) final = (Equilib Expression initial)n
Usually K is written without units
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Calculation of K
N2 + 3H2 3NH3Initial At Equilibrium[N2]0 =1.000 M [N2] = 0.921M[H2]0 =1.000 M [H2] = 0.763M[NH3]0 =0 M [NH3] = 0.157M
= 9.47X10-3322
23
]][[][
HNNHK =
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Calculation of KN2 + 3H2 3NH3Initial At Equilibrium[N2]0 = 0 M [N2] = 0.399 M[H2]0 = 0 M [H2] = 1.197 M[NH3]0 = 1.000 M [NH3] = 0.157MK is the same no matter what the amount of starting materials
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Symbols used for equilibrium constantK = used when the quantities of reactants and products are expressed as concentrations. That is mol/LThe symbol Kc is used in some books to express same value.Kp is used when the equilibrium involves gases and their quantities are expressed in partial pressures.
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13.3 Equilibrium Expressions Involving Pressures
Some reactions are involve gaseous materialsFor the sake of equilibria, the amounts of gases may be expressed as concentrations (mol/L) or pressures.Relationships between P & conc.:PV = nRTP = (n/V)RTP = CRTC is a concentration in moles/LiterC = P/RT
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Equilibrium and Pressure2SO2(g) + O2(g) 2SO3(g)
(PSO3)2
(PSO2)2 (PO2)
[SO3]2
[SO2]2 [O2]
Kp =
K = Kc=
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Relationship between K and Kp
K = (PSO3/RT)2
(PSO2/RT)2(PO2/RT)
K = (PSO3)2 (1/RT)2
(PSO2)2(PO2) (1/RT)3
(1/RT)2 = Kp RT(1/RT)3
K = Kp X
][(][][
22
2
23
OSOSOK =
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General Equation for the relationship between K and Kp
jA + kB lC + mDKp= (PC)l (PD)m= (CCxRT)l (CDxRT)m
(PA)j (PB)k (CAxRT)j(CBxRT)k
Kp= (CC)l (CD)mx(RT)l+m
(CA)j(CB)kx(RT)j+k
Kp = K (RT)(l+m)-(j+k) = K (RT)∆n
∆n=(l+m)-(j+k)=Change in moles of gas#moles of Products - #moles of reactants
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Homogeneous EquilibriaAll reactants and products are in one phase, gases for exampleK can be used in terms of either concentration or pressure.
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13.4 Heterogeneous EquilibriaIf the reaction involves pure solids or pure liquids as well as gases, the concentration of the solid or the liquid doesn’t change.As long as they are not used up they are left out of the equilibrium expression.Thus, there is no term for L or S in “K”expression.However, the presence of L or SL or S is a must for equilibrium to occur.
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Example: Equilibrium expression for heterogeneous equilibria
H2(g) + I2(s) 2HI(g)
But the concentration of I2 does not change.
]][[]['
22
2
IHHIK =
][][]['
2
2
2 HHIIK = K=
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Comments on heterogeneous EquilibriumPosition of equilibrium is independent of the amount of L or solid as long as some is presentL and S should be pure otherwise they cannot be neglected because their concentrations changeGases enter K expression as their partial pressureSolvents do not enter the K expressionsSpecies (ions or molecules) in water solution should enter the K expression as their molar concentrationsExample: CaCO3(s) CaO(s) + CO2 (g)
Kp = P CO2 K = [CO2]
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13.5 Applications of the equilibrium Constant
The magnitude of K helps prediction of the feasibility (extent or direction but not the speed) of the reactionK> 1; the reaction system consists mostly products (equilibrium mostly lies to the right)
Systems with very large K go mostly to completionSystems with very small values of K do not occur to any significant extent
There is no relation between the value of K and the time to reach equilibrium (the rate of reaction)
Time to reach equilibrium depends on Ea forreactants and products
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The Reaction Quotient, Q(Quantitative prediction of direction of reaction)
Q Tells how the direction of a reaction will go to reach equilibriumQ’s are calculated the same as K’s, but for a system not at equilibrium
[Products]coefficient
[Reactants] coefficient
aA(g) + bB(g) cC(g) + dD(g)
Q =
bB
aA
dD
cC
PXPPXPQ
)()()()(
=
Compare value of Q to that of K
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What Q tells us?If Q<K
Not enough productsEquilibrium shifts to right; forward reaction is predominant
If Q>K Too many productsEquilibrium shifts to left; reverse reaction is predominant
If Q=K system is at equilibrium; there is no further change
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Examplefor the reactionN2O4 (g) 2NO2(g)K = 11 at 100ºCIn an experiment 0.20 mol N2O4, 0. 20 mol NO2(g) are mixed in 4.0 L flask.Which direction will the reaction proceed to reach equilibrium?
][][
42
22
ONNOQ = K 0.05
(0.2/4)(0.2/4)2
<==
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Calculating equilibrium partial pressures and concentrations
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Example
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Example
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Example
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Example 13.9
At a certain temperature a 1.00-L flask contained 0.298 mol PCl3(g) and 8.70X10-3 mol PCl5(g). After the system had reached equilibrium, 2.00X10-3 mol Cl2(g) was found in the flask. Calculate the equilibrium conc. Of all species and the value of K
PCl5 PCl3(g) + Cl2(g)
Initial 8.70X10-3 mol 0.298 mol 0 mol
[ ] init 8.70X10-3 M 0.298 M 0 MChange -x +x +x
Equilib ? ? +2.00X10-3 M
K = ??
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Example 13.10Consider: CO (g) + H2O(g) CO2(g)+ H2(g)At 700K, K is 5.10. Calculate the equilibrium concentrations of all species if 1.00 mol of each component is mixed in 1.00L flask
CO (g) + H2O(g) CO2(g)+ H2(g)Initial 1 mol 1 mol 1 mol 1mol[ ] 1mol/1L 1mol/1L 1mol/1L 1mol/1L
Change -x -x +x +x
Equilib 1-x 1-x 1+x 1+x
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10.5)1()1(
)1)(1()1)(1(
2
2
=−+
=−−++
=xx
xxxxK
10.5)1()1(=
−+
xx
10.5)1()1(=
−+
xx
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13.6 Solving Equilibrium Problems
Given the starting concentrations and one equilibrium concentration.Use stoichiometry to figure out other concentrations and K.Learn to create a table of initial and final conditions.
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Consider the following reaction at 600ºC2SO2(g) + O2(g) 2SO3(g)In a certain experiment 2.00 mol of SO2, 1.50 mol of O2 and 3.00 mol of SO3 were placed in a 1.00 L flask. At equilibrium 3.50 mol SO3 were found to be present. Calculate the equilibrium concentrations of O2 and SO2, K and KP
2SO2(g) + O2(g) 2SO3(g)
Init 2.00 mol/L 1.50 mol/L 3.00 mol/L
Change -2X -X +2X
Equilib 3.50 mol/L
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What if equilibrium concentrationis not given?
The size of K will determine what approach to take.First let’s look at the case of a LARGE value of K ( >100).Simplifying assumptions can be made.
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ExampleH2(g) + I2(g) 2HI(g)K = 7.1 x 102 at 25ºCCalculate the equilibrium conc. if a 5.00 L container initially contains 15.9 g of H2 and 294 g of I2 .[H2]0 = (15.7g/2.02)/5.00 L = 1.56 M [I2]0 = (294g/253.8)/5.00L = 0.232 M[HI]0 = 0
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Q= 0<K so more product will be formed.Assumption: since K is large reaction will go to completion.Stoichiometry tells us I2 is LR, it will be smallest at equilibrium Set up table of initial, change and equilibrium concentrations.
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H2(g) I2(g) HI(g)initial 1.56 M 0.232 M 0 Mchange -0.232 -0.232 +0.232X2Final 1.328 0 +0.464
(before the reverse reaction takes place)When the reverse reaction takes place to
achieve an equilibrium a decrease of 2x will take place in HI and an increase of x in each of H2 and I2 will take place
Thus final concentrations will be taken as the initials
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H2(g) I2(g) 2HI(g)Initial 1.328 0 +0.464Change +X +X -2XEquilib 1.328+X X 0.464-2X
Now plug these values into the equilibrium expression
(0.464-2X)2 = 7.1 x 102
(1.328+X)(X)
When we solve for X we get 2.8 x 10-4
K =
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Can we eliminate X from the equation?
K = (0.464-2-X)2 = 7.1 x 102
(1.328+X)(X)Since X is going to be small, we can ignore it in relation to 0.464 and 1.328So we can rewrite the equation7.1 x 102 = (0.464)2
(1.328)(X)This makes the algebra easy
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When we solve for X we get 2.8 x 10-4
X was also without approximation 2.8 x 10-4
So we can find the other concentrationsI2 = 2.8 x 10-4 MH2 = 1.328 M HI = 0.464 M
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Problems with small K
K< .01
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For exampleFor the reaction
2NOCl 2NO +Cl2K= 1.6 x 10-5
If 1.0 mol NOCl, is placed in 2.0L flask What are the equilibrium concentrations?
Since there are no products exist intially, the system will move to the right to reach equilibrium[NOCl]0 = 1.0 mol/2.0L = 0.50M
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K = 1.6X10-5 = This equation is complicated; an approximation is needed
2NOCl 2NO Cl2Initial 0.50M 0 0
Change -2x +2x + x
Equilib. 0.50-2x 2x x
2
2
22
2
)250.0()()2(
][][][
xxx
NOClClNO
−=
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2
2
22
2
)250.0()()2(
][][][
xxx
NOClClNO
−=K = 1.6X10-5 =
0.50-2x ≈ 0.50
2
3
2
2
)50.0(4
)50.0())(2( xxx= = K = 1.6X10-5
X = 1.0X10-2
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13.7 Le Chatelier’s Principleif a change is imposed on a system at equilibrium, the position of the equilibrium will shift in a direction that tends to reduce that change.If a stress is applied to a system at equilibrium, the position of the equilibrium will shift to reduce the stress.There are 3 Types of stress
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External conditions that cause a disturbance to a chemical equilibrium
Adding or removing reactants or productsChanging the volume (or pressure) of the systemChanging the temperature
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The effect of a change in concentration of reactants and/or products
The system will shift away from the added component
Adding product makes Q>KRemoving reactant makes Q>KAdding reactant makes Q<KRemoving product makes Q<K knowing the effect on Q, will tell you the direction of the shiftAdding or removing liquids or solidsdoes not affect the equilibrium
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The effect of a Change in Pressure
The pressure changes as a result of:Adding or removing gaseous reactant or
productAdding an inert gasChanging the volume of the container
Adding inert gas does not affect the equilibrium position; conc. or P will not change.
By reducing the volume of the container, the system will move in the direction that reduces its volume.
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The effect of a Change in Pressure
The system will respond to the decrease in volume by decreasing the total number of gaseous molecules in the system.
At constant temp and pressure the volume of a gas is directly proportional to the number of moles of gas present
n
PRTV
nRTPV
)(=
=
Thus Vα n
Thus V Thus V αα nn
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Change in TemperatureAffects the rates of both the forward and reverse reactions.changes the equilibrium constant.The direction of the shift depends on whether it is exo- or endothermic
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Exothermic∆H<0Releases heatThink of heat as a productRaising temperature push toward reactants.Shifts to left.
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Endothermic∆H>0Heat is added to the systemThink of heat as a reactantRaising temperature push toward products.Shifts to right.
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Learning Outcomes• Explain how dies a system reach
equilibrium.• Explain how does equilibrium work as a
dynamic process.• Write the equilibrium constant expression
according to the law of mass action• Write K for the reversible reaction; for a
reaction whose coefficients are multiplied by any integer; and for a reaction that represents the summation of more than one reaction
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• Relating Kp to K (Kc)• Write equilibrium expression for
reactions involving heterogeneous equilibria.
• Explain what is meant by equilibrium position.
• Predict the direction of equilibrium position from the value of the Quotient, Q by comparing Q with K
• Solve equilibria problems• Apply Le Chaetelier’s principle