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Kinetic Collision Theory

The main ideas of the collision-reaction theory are as follows:

• A chemical sample consists of particles (atoms, ions, or molecules) that are in constant
random motion at various speeds, rebounding elastically from collisions with each other.
The average kinetic energy of the particles is perceived as the temperature of the sample.

• A chemical reaction must involve collisions of reactant particles.

• An effective collision requires sufficient energy and correct orientation (positioning) of the
colliding particles so that bonds can be broken and new bonds formed.

• Ineffective collisions involve particles that rebound from the collision, essentially unchanged
in nature.

• The rate of a given reaction depends on two factors related to collisions: the frequency of
collisions and the fraction of those collisions that are effective.

Factors Affecting Reaction Rates:


The explanation of factors affection reaction rates is as follows:

• A minimum activation energy (the energy of the activated complex) is required for a collision
between particles to be effective, that is, energetic enough to cause the breaking and
forming of bonds to product new particle structures

• Many reactions occur as a sequence of elementary process, or two particle-collision steps,


which make up the overall reaction mechanism.

• The rate of any reaction depends on the nature of the chemical substances reacting
because both the strength of bond(s) to be broken and the location of the bond(s) in the
particle structure affect the likelihood that any given collision is effective.

• An increase in reactant concentration or in reactant surface area increases the rate of a


reaction because the total number of collisions possible per unit time is increased
proportionately. Concentration – [reactant] ([ ] = concentration) , Rate , Surface Area –
Surface Area , Rate 

• An increase in temperature increases the rate of a reaction for two reasons. The total
number of collisions possible per unit time is increased slightly, but more importantly, the
fraction of collisions which are energetic enough to be effective is increased dramatically.
Temperature – Temp , Rate  (and vice-versa)

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 1 OF 26


• A catalyst increases the rate of a reaction by providing an alternative pathway to the same
product formation that has a lower activation energy. A much larger fraction of collisions is
effective following the changed reaction mechanism. Catalysts are involved in the reaction
mechanism at some point, but are regenerated before the reaction is complete.

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 2 OF 26


Kinetic Collision Theory
1. Reaction Mechanism: individual steps during the process of a reaction.

2. Reaction Rate or Rate of Reaction: change in amounts of reactants or products over time.

3. Rate-Determining Step: the slowest reaction step in any reaction mechanism. It has a fairly
high “activation energy” and the rate of the overall reaction is controlled by this step.

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 3 OF 26


Kinetic Collision Theory (Potential Energy Diagram)
Exothermic Reaction
Exothermic reactions are always negative.

Endothermic Reaction
Endothermic reactions are always positive.

Things to Remember:
• Always start at zero.
• Endothermic = +
• Exothermic = -
• Label the diagram!

• Eact(rev)  +∆H + Eact(fwd)

• Eact(fwd)  -∆H + Eact(rev)

• ∆H  If stated, the other ∆H is either positive or negative.


• Put all information that is given to you on your diagram.
• If you are only given a chemical formula, then you must use Hess’s Law of Heat Summation
(Formations) to determine the ∆H value. You will only need to draw a PE (potential energy)
diagram for the value of ∆H and nothing else. For example: if ∆H is negative, then you draw
a PE diagram for below zero (Exothermic), and vice-versa.

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 4 OF 26


Questions for the Kinetic Collision Theory (Potential Energy
Diagram)
1. Carbon monoxide, CO, reacts with nitrogen dioxide, NO2. Carbon dioxide, CO2, and nitric
oxide, NO, are formed. Draw a potential energy diagram to illustrate the progress of the
reaction. Label the axis, transition state, and the activated complex. Indicate the activation
energy for the forward reaction, Eact(fwd) = 134 Kj, as well as ∆H = -226 Kj. Calculate the
activation energy for the reverse reaction, Eact(rev), and show it on the graph.

CO (g) + NO2 (g)  CO2 (g) + NO (g)

Eact(fwd) = 134 Kj
∆H = -226 Kj
* Eact(rev) = ? (360 Kj)
* ∆H = + 226 Kj

* Indicates that you are/have solving/solved for


these variables.

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 5 OF 26


Kinetic Collision Theory (Reaction Intermediates)
Reaction Intermediates are substances that are formed during the reaction, but immediately
react again and are not present when the reaction is complete.

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 6 OF 26


Questions for the Kinetic Collision Theory (Reaction
Intermediates)
1. A chemist proposes the following mechanism. Write the overall balanced equation. Identify
any reaction intermediate.

Step 1 : NO2 (g) + F2 (g)  NO2F (s) + F (s)


Step 2 : NO2 (g) + F (s)  NO2F (s)
---------------------------------------------
2NO2 (g) + F2 (g)  2 NO2F (s)

F (s) is the reaction intermediate. It is a product in the first step, it becomes a reactant in the
second step, and it is not present in the overall formula.

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 7 OF 26


Kinetic Collision Theory (Catalysts)
A catalyst is a substance that increases the rate of a chemical reaction without being consumed
by the reaction. Catalysts are of tremendous importance in all facets of chemistry, from the
laboratory to industry. A catalyst works by lowering the activation energy of a reaction so that a
larger fraction of the reactants have sufficient energy to react. It lowers the activation energy by
providing an alternative mechanism for the reaction.

Things to Remember:
• The activation energy decreases and the ∆H remains the same when a catalyst is added to
a reaction.
• A catalyst changes the activation energy of the reaction.

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 8 OF 26


Questions for the Kinetic Collision Theory (Catalysts)
1. Consider the following reaction:

2A + B2  D + E

A chemist proposes the following reaction mechanism:

Step 1 : A + B2  AB2
Step 2 : AB2 + C  AB2C
Step 3 : AB2C + A  A2B2 + C
Step 4 : A2B2  D + E

(a) What is the roll of AB2C and AB2?


 AB2C and AB2 are both reaction intermediates.

(b) What is the role of C?


 C is a catalyst, as it is a reactant first, then a product, and it is not in the final, overall formula.

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 9 OF 26


Reversible Reactions and Chemical Equilibrium
1. Dynamic Equilibrium: occurs when opposing changes are occurring at the same time and at
the same rate. For instance: a jar that is sealed with water. The water evaporates and
condenses at the same time, and at the same rate.

2. Homogenous Equilibrium: reactants and products are in the same phase (state of matter –
solid, liquid, gas).

3. Heterogeneous Equilibrium: reactants and products are in a different phase.

The Four Conditions That Apply to all Equilibrium Systems:

1. Equilibrium is achieved in a reversible process when the rates of opposing changes are
equal.

 H2O (l) H2O (g)


 H2 (g) + Cl2 (g) 2HCl (g)

2. The observable properties of a system at equilibrium are constant (color, pressure,


concentration, and pH level).

3. Equilibrium can only be achieved in a closed system – does not allow anything to escape or
enter.

4. Equilibrium can be approached from either direction (left to right, or, right to left).

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 10 OF 26


The Equilibrium Constant
The Law of Chemical Equilibrium states, at equilibrium, there is a constant ratio between the
products and reactants in any change.

For any general equilibrium reaction: aP + bQ cR + dS

[ R ]c [ S ]d products
Kc =
[ P ]a [ Q ]b reactants

Where “Kc” is the equilibrium at constant, “a, b, c, d” are the coefficients of “P, Q, R, S”, and [ ]
is the concentration in mols/litre.

Things to Remember:
• When solving for “Kc”, you do not have to use units, for instance: mol, litres, or mol/l.
• If a problem states “mol”, then you must divide the numbers of mol by the litres to obtain
“mol/l”.
• Pure liquids and solids are not included (this is in relation to the subscript of each chemical
compound, (l) and (s)).
• If the coefficient (either a, b, c, d) is 1, do not write it as a superscript number in the general
equilibrium reaction formula, as it is understood to already be there.
• If there is only 1 product or reactant when calculating “Kc”, replace with a 1.

• If a problem states that products or reactants are initially a number, do not use these
numbers when determining “Kc” or a product or reactant; you must only use numbers when
it states that they are at “equilibrium”.

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 11 OF 26


Questions for The Equilibrium Constant
1. The reaction between propane and oxygen to form carbon dioxide and water vapour:

C3H8 (g) + 5O2 (g) 3CO2 (g) + 4H20 (g)

[ R ]c [ S ]d
Kc =
[ P ]a [ Q ]b

[ CO2 (g) ]3 [ H2O (g) ]4


Kc =
[ C3H8 (g) ] [ O2 (g) ]5

2. A mixture of nitrogen and chlorine gases was kept at a certain temperature in a 5.0 litre
reaction flask. When the equilibrium mixture was analyzed, it was found to contain 0.0070 mol of
N2 (g), 0.0022 mol of Cl2 (g), and 0.95 mole of NCL3 (g). Calculate the equilibrium constant for
this reaction.

N2 (g) + 3Cl2 (g) 2NCl3 (g)

[ N2 (g) ] = 0.0070 mols ÷ 5.0 l = 0.0014 mols/l


[ Cl2 (g) ] = 0.0022 mols ÷ 5.0 l = 0.00044 mols/l
[ NCl3 (g) ] = 0.95 mols ÷ 5.0 l = 0.19 mols/l

[ NCl3 (g) ]2
Kc =
[ N2 (g) ] [ Cl2 (g) ]3

[ CO2 (g) ]2 [ H2O (g) ]4


Kc =
[ C3H8 (g) ] [ Cl2(g) ]3

(0.19) 2
Kc =
(0.0014)(0.00044) 3

0.036
Kc =
(1.19 x 10 -13)

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 12 OF 26


Kc = 3.03 x 10 11

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 13 OF 26


Le Châtelier’s Principle
When a chemical system at equilibrium is disturbed by a change in a property of the system, the
system adjusts to oppose the change.

Variables Direction of Change Response of System

Shifts to consume some of the added reactant or


Concentration Increase
product.

Shifts to replace some of the removed reactant or


Decrease
product.

Temperature Increase Shifts to consume some of the added heat.

Decrease Shifts to replace some of the removed heat.

Shifts toward the side with the larger total amount


Volume (Overall pressure) Increase (decrease in pressure)
of gaseous entities.

Shifts toward the side with the smaller total


Decrease (increase in pressure)
amount of gaseous entities.

Catalyst Added to the reaction No effect.

Things to Remember:
• If “energy” or “kj” is stated on the left side (reactants), it is considered to be endothermic;
however, if it is stated on the right side (products), it is considered to be exothermic.

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 14 OF 26


Examples for Le Châtelier’s Principle
Concentration:
A few crystals of OH- are added.
H20 (l) H+ (aq) + OH- (aq)
 Effect: shift left

CO2 (g) is removed from the container.


CaCO3 (s) + energy CaO (s) + CO2 (g)
 Effect: shift right

Temperature:
The container is heated.
H2O (l) + energy H2O (g)
 Effect: shift right

Energy is removed.
2SO2 (g) + O2 (g) 2SO3 (g) + energy
 Effect: shift right

Volume (Overall Pressure):


The volume is decreased (increase in pressure).
N2 (g) + 3H2 (g) 2NH3 (g)
 Effect: shift right

The volume is increased (decrease in pressure).


2NO (g) + O2 (g) 2NO2 (g)
 Effect: shift left

The volume is decreased (increase in pressure).


H2 (g) + I2 (G) 2HI (g)
 Effect: no effect (the coefficients are equal)

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 15 OF 26


Finding Equilibrium Amounts for Initial Amounts and Kc
(Quadratics)

Problem:
The following reaction has an equilibrium constant of 25.0 at 1100 K.

H2 (g) + I2 (G) 2HI (g)

2.00 mol of H2 (g) and 3.00 mol of I2 (g) are placed in a 1.00 litre reaction vessel at 1100 K.
What is the equilibrium concentration of each gas?

What is Required?
You need to find [ H2 (g) ], [ I2 (g) ], and [ HI (g) ].

What is Given?
You have the balanced chemical equation. You know the equilibrium constant for this reaction,
Kc = 25.0. You also know the concentrations of the reactants and product: [ H2 (g) ]i = 2.00
mol/l, [ I2 (g) ]i = 3.00 mol/l, and [ HI (g) ]i = 0.

Plan Your Strategy:

Step 1: Set up an ICE table. Let the change in molar concentrations of the reactants be x. Use
the stoichiometry of the chemical equation to write expressions for the equilibrium
concentrations. Record these expressions in your ICE table.

Step 2: Write the equilibrium expression. Substitute the expressions for the equilibrium
concentrations into the equilibrium expression. Rearrange the equilibrium expression into the
form of a quadratic equation. Solve the quadratic equation for x.

Step 3: Substitute x into the equilibrium line of the ICE table to find the equilibrium
concentrations.

Act on Your Strategy:


Step 1: Set up an ICE table.

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 16 OF 26


Concentration (mol/l) H2 (g) + I2 (g) 2HI (g)

Initial 2.00 3.00 0

Change -x -x +2x

Equilibrium 2.00 - x 3.00 - x +2x

Finding Equilibrium Amounts for Initial Amounts and Kc


(Quadratics) Continued…
Step 2: Write and solve the equilibrium expression.

[ HI (g) ]2
Kc =
[ H2 (g) ] [ I2 (g) ]

(2x) 2
25.0 =
(2.00 – x)(3.00 – x)

(2X)2
25.0 =
(6.00 – 2.00 x -3.00x + x2)

This equation does not involve a perfect square. It must be re-arranged into a quadratic
equation.

4x2
25.0 =
(6.00 – 5.00x + x2)

6.00 – 5.00x + x2 = 4x2 ÷ 25.0


6.00 – 5.00x + x2 = 0.16 x2
6.00 – 5.00x + x2 – 0.16x2 = 0
0.840x2 – 5.00x + 6.00 = 0

-b + √b22 – 4ac
x=
2a

-(-5.00) + √(-5.00)2 – 4(0.840)(6.00)


x=
2(0.840)

5.00 + √25 – 20.16


x=
1.68

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 17 OF 26


5.00 + √4.84
x=
1.68

x= 4.3 and 1.7

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 18 OF 26


Finding Equilibrium Amounts for Initial Amounts and Kc
(Quadratics) Continued…
Step 3: The value x = 4.3 is not physically possible. It would result in negative concentrations of
H2 (g) and I2 (g) at equilibrium. The concentration of each substance at equilibrium is found by
substituting x = 1.7 into the last line of the ICE table.

[ H2 (g) ] = 2.00 – x
[ H2 (g) ] = 2.00 – 1.7
[ H2 (g) ] = 0.3 mol/l

[ I2 (g) ] = 3.00 – x
[ I2 (g) ] = 3.00 – 1.7
[ I2 (g) ] = 1.3 mol/l

[ HI (g) ] = 2x
[ HI (g) ] = 2(1.7)
[ HI (g) ] = 3.4 mol/l

Check Your Solution:


The coefficients in the chemical equation match the exponents in the equilibrium expression. To
check your concentrations, substitute them back into the equilibrium expression.

(3.4)2
25.0 =
(0.3)(1.3)

(3.4)2
25.0 =
0.39

11.56
25.0 =
0.39

25.0 = 29.64

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 19 OF 26


Solving the quadratic equation gives a value of x, correct to one decimal place. As a result, [ H2
(g) ] can only have one significant figure. The calculated value of “Kc” is equal to the given
value, within the error introduced by rounding.

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 20 OF 26


Finding Equilibrium Amounts for Initial Amounts and Kc (Perfect
Square)

Problem:
The following reaction increases the proportion of hydrogen gas for use as a fuel.

CO (g) + H2O (g) H2 (g) + CO2 (g)

This reaction has been studied at different temperatures to find the optimum conditions. At 700
K, the equilibrium constant is 8.3. Suppose that you start with 1.0 mol of CO (g) and 1.0 mol of
H2O (g) in a 5.0 litre container. What amount of each substance will be present in the container
when the gases are at equilibrium, at 700 K?

What is Required?
You need to find the amount (in mols) of CO (g), H2O (g), H2 (g), and CO2 (g) at equilibrium.

What is Given?
You have the balanced chemical equation. You know the initial amount of each gas, the volume
of the container, and the equilibrium constant.

Plan Your Strategy:

Step 1: Calculate the initial concentrations, if needed.

[ CO (g) ] = 1.0 mol ÷ 5.0 L = 0.2 mol/l


[ H2O (g) ] = 1.0 mol ÷ 5.0 L = 0.2 mol/l

Step 2: Set up an ICE (initial, change, and equilibrium) table. Record the initial concentrations
you calculated in step 1 in your ICE table. Let the change in molar concentrations of the
reactants be x. Use the stoichiometry of the chemical equation to write the record expressions
for the equilibrium concentrations.

Concentration (mol/l) CO (g) + H2O (g) H2 (g) + CO2 (g)

Initial 0.2 0.2 0 0

Change -x -x +x +x

Equilibrium 0.2 - x 0.2 - x 0+x 0+x

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 21 OF 26


UNIT 5: KINETICS AND EQUILIBRIUM PAGE 22 OF 26
Finding Equilibrium Amounts for Initial Amounts and Kc (Perfect
Square) Continued…
Step 3: Write the equilibrium expression. Substitute the expressions for the equilibrium
concentrations into the equilibrium expression. Solve the equilibrium expression for x.

[ H2 (g) ] [ CO2 (g)]


Kc =
[ CO (g) ] [ H2O (g) ]

(x)(x)
8.3 =
(0.2 – x)(0.2 – x)

(X)2
8.3 =
(0.2 – x)2

√ (X)2
√8.3 =
√ (0.2 – x)2

(x)
+ 2.88 =
(0.2 – x)

+ 2.88 (0.2 - x) =x

+ 2.88 (0.2 - x) =x

0.576 ÷ 3.88 = 3.88x

0.148 =x

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 23 OF 26


- 2.88 (0.2 - x) =x

Finding Equilibrium Amounts for Initial Amounts and Kc (Perfect


Square) Continued…

- 0.576 ÷ -1.88 = -1.88x

0.306 =x

Step 4: The value x = 0.306 is physically impossible because it would result in a negative
concentration of both CO (g) and H2O (g) at equilibrium.

Therefore:

[ H2 (g) ] = 0.148 mol/l


[ CO2 (g) ] = 0.148 mol/l

[ CO (g) ] = 0.20 – x
[ CO (g) ] = 0.20 – 0.148
[ CO (g) ] = 0.052

[ H2O (g) ] = 0.20 – x


[ H2O (g) ] = 0.20 – 0.148
[ H2O (g) ] = 0.052

To find the amount of each gas, multiply the concentrations of each gas by the volume of the
container (5.0 litre in this case).

Amount of H2 (g) = CO2 (g) = 0.75 mol


Amount of CO (g) = H2O (g) = 0.25 mol

Check Your Solution:


The equilibrium expression has product terms in the numerator and reactant terms in the
denominator. The amounts of chemicals at equilibrium are given in mols. Check “Kc”.

(0.75)2
8.3 =
(0.25)2

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 24 OF 26


8.3 = 9.0

Finding Equilibrium Amounts for Initial Amounts and Kc (Perfect


Square) Continued…
This is close to the given value, Kc = 8.3. The difference is due to some mathematical rounding.

Things to Remember:
• “x” will always be negative on the reactant side, while “x” will always be positive on the
product side.
• Be sure to use the coefficient on the chemical compound. For example: 2HI(g).

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 25 OF 26


Questions for Finding Equilibrium Amounts for Initial Amounts
and Kc
1. A chemist was studying the following reaction.

SO2 (g) + NO2 (g) (g) NO (g) + SO3 (g)

In a 1.0 litre container, the chemist added 1.7 x 10-1 mol of SO2 (g) to 1.1 x 10-1 mol of NO2 (g).
At equilibrium, the concentration of SO3 (g) was found to be 0.089 mol/l. What is the value of
“Kc” for the reaction at this temperature?

[ SO2 (g)]i = 1.7 x 10-1 mol ÷ 1.0 l = 1.7 x 10-1 mol mol/l
[ NO2 (g)]i = 1.1 x 10-1 mol ÷ 1.0 l = 1.1 x 10-1 mol/l

Concentration (mol/l) SO2 (g) + NO2 (g) NO (g) + SO3 (g)

Initial 1.7 x 10-1 1.1 x 10-1 0 0

Change - 0.089 - 0.089 + 0.089 + 0.089

Equilibrium 0.081 0.021 0.089 0.089

[ NO (g) ] [ SO3 (g) ]


Kc =
[ SO2 (g) ] [ NO2 (g) ]

(0.089)(0.089)
Kc =
(0.081)(0.021)

0.007921
Kc =
0.001701

Kc = 4.7 (rounded)

UNIT 5: KINETICS AND EQUILIBRIUM PAGE 26 OF 26

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