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Wednesday, 2 March 2011

11.3 Reaction Kinetics

11.3 Factor Affecting Reaction Rate
Objectives
1.    Explain factors affecting reaction rate;

              -Concentration / Pressure   -Temperature
              -Catalyst                              -Particle size

    2. Explain the effect of temperature on reaction
        rate using Maxwell-Boltzmann distribution
        curve.

    3. Explain the effect of catalyst on activation
       energy based on energy profile diagram for
       exothermic and endothermic reactions.
   4. Relate rate constant to temperature and activation energy using the Arrhenius   
       equation
      
       k = Ae-Ea/RT or ln k = ln A –Ea/RT

   5. Determine k, Ea, T and A using Arrhenius
       equation by calculation and graphical method.


Ln (k1 / k2) = Ea/R (1/T2 – 1/T1)



Factors Affecting Reaction rate
a) Effect of Concentration
o When concentration of reactant increases, frequency
of collision also increases.
o More particles present in the same volume, they are more likely to collide
o The probability of effective collisions increase

frequency of effective collision = collision frequency x fraction of molecules with
                                                                                           sufficient energy

o Rate of reaction increases.
   [reactants] increases,the frequency of collision increases
o This observation correlates with the RATE LAW that has been previously  discussed…



    Reaction rate = k [ A ]x [ B ]y …
                             (A & B = reactants)
                            (x & y = rate order)

o Based upon this equation,
                       Reaction rate directly proportional to the concentration of reactants

o REMINDER!
    Only in zero order reactions, the rate of reaction is not
    dependant upon the concentration of the reactants.
    (depending on its rate order)
    Reaction rate = k [ A ]0 = k (constant)
b) Effect of Temperature
o At a higher temperature, molecules have higher kinetic energy and move at higher speed
o more collisions will occur in a given time
o Furthermore, the higher the KE, the higher the energy of the collisions
o So more molecules will have energy greater than Ea
o effective collision also will be increased
o thus the reaction rate increases.
Distribution of Kinetic of Molecules(Maxwell-Boltzmann Distributions)


The collision frequency is higher temperature because the fraction of reactant molecules with activation energy is higher.
Maxwell-Boltzmann Distributions
• The figure shows the distribution KE of gaseous molecule at temperature T1 and T2.
• At higher temperature, the fraction of molecules with energy greater than Ea increases.axwel-Boltzmann Distributions
• Thus, rate of reaction increase with increase of
temperature.
Take note:
• Area under the curve ∝ to the total number of molecules
area under the curve is the same, bcoz no. of molecules is the same.
Maxwel-Boltzmann Distributions
• There are a wide range of molecular energy
A few molecules have low and high KE, most have value in the middle.

• The shape of the graph changes with temperature
At higher temperature the peak of the graph moves towards the right to a higher KE value as the curve broadens out.


• At higher temperatures, the fraction of molecules with higher energy increase
Average energy increase at higher temperature, but fraction of molecules with low energy decreases. At higher temperature, fraction of molecules with energy
greater than Ea increase.
Effect Of Temperature
ARRHENIUS EQUATION

• the effect of temperature on the rate constant, k:

                                k = A e -Ea⁄RT

Where…
k = rate constant
A = frequency factor
(is a measure of the probability of a favorable collision)
e = natural log exponent
Ea = activation energy for the reaction (kJ/mol)
R = universal gas constant (8.314 J mol-1 K-1)
T = absolute temperature (T in Kelvin)
Arrhenius Equation - Derivation

  k = A e^ -Ea⁄RT

ln k = ln (A.e^ –Ea/RT)



ln k = ln A – Ea/RT


ln k = ln A - Ea / R (1/T)


   y = C + mx



Example

The table below gives the rate constants, k for the reaction between potassium hydroxide and bromoethane at different temperatures.

K(M^-1s^-1)
T(k)
0.63
322
2.50
331
10.0
347
22.6
353

a) Using a graphical method, calculate the activation energy (kJmol-1) for this reaction.
b) What is the overall order of reaction? Explain
c) Calculate the initial rate of reaction at 330 K when the concentrations for both KOH and   CH3CH2Br are 0.1M.

Solution……

1/T
0.0031
0.0030
0.0029
0.0028
ln k
-0.46
0.92
2.30
3.12

a) Slope = Ea/R
              = 12492
Ea = 12492 × 8.314
     = 1.04 ×105 Jmol-1
     = 104 kJmol-1

b) Second order, unit of k = M-1s-1

 c) ln k = -Ea/R(1/T) + ln A
     ln k = -12492 (1/330) + 38.45
         k = 1.81 M^-1s^-1

Rate = k [KOH][CH3CH2Br]
        = 1.81 x 0.1 x 0.1
        = 1.81 x 10-2 Ms-1
Arrhenius Equation – Further Derivation

Rate constant, k varies with T.
The ratio of rate constant at two different T can be calculated.

ln k1 = ln A – Ea / RT1……………………….(1)
ln k2 = ln A – Ea / RT2……………………….(2)
Equation (1) minus (2) gives :
ln ( k1/k2) = Ea / R (1/T2-1/T1)
Effect Of Catalyst
• A catalyst is a substance that increases the rate of a chemical reaction without itself being consumed.
• It increases the reaction rate by providing an alternative reaction pathway of which having lower activation energy.
• A catalyst provides a different reaction mechanism.

A catalyst provides an alternative pathway for the reaction to occur (----curve) which has a lower activation energy.



When Ea decreases, k increases, reaction rate increases

Effect Of Surface Area
• For reactions that occur on a surface that is for solid, the rate increases as the surface
area is increased.

• A larger surface area increases the contact area between the reactants thus increases
the frequency of collision and the probability of effective collision between the molecules
of the reactants.


Tuesday, 1 March 2011

11.2 Collision Theory And Transition State Theory

Objectives
1.Collision theory.
   Explain the requirements for effective collision:
      i. minimum energy
     ii. Correct orientation

2. Transition state theory
    i. Define activation energy of a reaction with reference to the energy profile      diagram.
   ii. Define activated complex.
  iii. State the characteristics of an activated complex.

Collision Theory
Collision Theory is the theory to explain the rate of chemical reactions. It is based on;
1-    molecule must collide to react
2-    molecules must possess a certain minimum kinetic energy (activation energy) to initiate the chemical reaction .
3-    molecule must collide in the right orientation in order that the collisions will result  in a reaction.

Only effective collisions cause formation of product that is collisions of molecules with Ea and at correct orientation.        



Rate directly proportional to the number of effective collisions / time


           
Activation Energy

The activation energy (Ea) is the min. kinetic energy that molecules must posses in order for a chemical reaction to occur. The Ea is shown on reaction profiles diagrams, illustrate the role of the Ea as an energy barrier that must be overcome by the reactants before they can form products.

Orientation factor/stearic factor : is how reacting molecules are oriented relative to each other.
·         Collision that cannot produce chemical change(ineffective collision)
·         Collision that lead a reaction(effective collision)

Transition State Theory

o The transition state theory describes what happens to the reactant molecules prior to their change into products.
o An intermediate stage lies between the reactants and the products is transition state.
o The transitional species with partial bonds is activated complex.

A Reaction Profile

Characteristics Of An Activated Complex

• Very unstable, It has a short half-life (exists at the instant the reacting system has the highest potential energy.
• Its potential energy is greater than reactants or products.
• In an activated complex, the bonds in the reactant molecules are in the process of breaking while the new bonds in the product molecules are starting to form.
• The activated complex and the reactants are in chemical equilibriumharacteristics
• It decomposes to form products or reactants.

Example


1. Define the term activation energy
2. Draw a potential energy diagram for an endothermic reaction. Indicate on the
drawing
    i. the potential energy of reactants
   ii. the potential energy of the products
  iii. the energies of activation for the forward and reverse reactions
  iv. the heat of reaction.

Solution

The activation energy (Ea)…..is the minimum energy is required
to initiate the chemical reaction and produce the product. It must be
supplied by collisions.

Study Chem!!!!!!

Characteristics Graphs for Zero Order Reaction
       
Rate = k[A]o
[A]o – [A]t = kt
[A]t = [A]o – kt
Y    = C + mx
Integrated Rate Equation
            For reaction, A to forms products
b) For first-order reaction
    Rate = - d[A] / dt              Rate = k [A]1
The differential rate equation : - d[A] / dt = k[A]
The integrated rate law :


Ln[A]o – ln[A]t = kt



Half life (t ½) of a first-order reaction

            Since, ln [A]o / [A]t = kt
Substituting t = t ½ ,            [A]t = [A]o / 2

Ln [A]o / ([A]o/2) = kt ½


t ½ = ln2 / k



Characteristic Graph For First-Order Reaction

Rate = k [A]
Ln[A]o – ln[A]t = kt
Graph of half life(t ½) for First-Order Reaction

t ½ = ln2 / k
t ½ is independent of initial concentration t1 = t2

Jom Explore!!!!!!


The Order Of Reaction


OBJECTIVES

1. Write the integrated rate laws for zero order, 1st order and 2nd order reaction
2. Define half-life.
3. Draw the respective graphs for the different order reactions.
4. Solve quantitative problems.


For Reaction,

               A To form Products

                         Rate = k [A]x

i)If x=0              Rate = k [A]0
                         Rate = k

Rate is not dependent on [A]

Thus, this reaction is zero order with respect to A



              A To form Products

                          Rate = k [A]x

ii) If x=1              Rate = k [A]1
                     
    If the [A] will double the rate of reaction.

Thus, this reaction is  first order with respect to A



              A To form Products

                          Rate = k [A]x

iii) If x=2              Rate = k [A]2

Doubling the [A],the rate increase by a factor of 4.

Thus,the reaction is second order with respect to A

Reaction Kinetics(11.1)

Objective


  1. define rate laws,order of reaction and rate constant
  2. write the rate law/rate equation
  3. calculate the order with respect to a certain reactant and the overall order of reaction from the experimental data
  4. calculate the value and determine the units of rate constants,k.
The Rate Law


  • The rate law for a chemical reaction relate the rate of reaction to the concentrations of reactants.
  • At constant T&P,rate of chemical reaction directly proportional to [reactants]
Rate directly proportional to [reactants]

Consider this equation:

                                  aA + bB to cC                                                k = rate constant 
                                  Rate directly proportional to [reactants]          m = reaction order with respect to A
                                  Rate = k[A]m[B]n                                          n = reaction order with respect to B
                                                                                                   m+n = overall reaction order

  • The exponents in a rate law/ reaction order must be determined by experiment.They are not derived from the stoichiometric coefficients in an overall chemical equation.They are generally small,positive integers (0,1,2......)
  • The rate constant,k and its value depends on specific reaction,T& the presence of catalyst.The larger k,the faster the reaction proceeds.Units of k depends on the values of m,n.....
Example 1

determining reaction order from Rate Laws

2NO(g) + O2(g) TO 2NO2(g)                 (rate = k[NO2]2[O2])

Solution:

The reaction order with respect to NO =2
The reaction order with respect to O2 = 1
The overall reaction order =3

Example 2

S2O8 + 3I to 2SO4 + I3

The above reaction is first order with respect to iodide and to thiosulphate ion

a)Write the rate equation for the reaction
b)What is the unit of rate constant,k?

Solution:

a) Rate = k [S2O8]-1[I]-1
b) Rate = k[S2O8]1[I]1

               k = rate/([S2O8]1[I]1 = Ms-1/M2 = M-1S-1

Determine rate law:Method of Initial Rates
 ine rate law: Method Of Initial Rates
• The method of initial rates involves a series of expt in which the initial [ ] of some reactants are held constant and others are varied in order to determine the rate law for that reaction.
• The effects of doubling one initial concentration:
·         For zero-order reactions, no effect on rate.
·         For first-order reactions, the rate doubles.
·         For second-order reactions, the rate quadruples.
·         For third-order reactions, the rate increases
             eightfold.

Method Of Initial Rates

Initial Rates of the Reaction:

2NO(g) + Cl2(g)  to 2NOCl(g)



   Exp.
Initial [NO]
Initial [Cl2]
Initial rate,Ms-1
1
0.0125
0.0255
2.27 x 10-5
2
0.0125
0.0510
4.55 x 10-5
3
0.0250
0.0255
9.08 x 10-5



d
2NO(g) + Cl2(g) To 2NOCl(g)

The rate law in general is; Rate = k [NO]m [Cl2]n,Compare 2 experiments,of [one reactant] varies and the [other reactant] constant.

Rate exp2/Rate exp1 = k[NO]exp2(m) [Cl2]exp2(N) / k[NO]exp1(m) [Cl2]exp1(n)
4.55x10-5/2.27x10-5  = k(0.0125)m (0.0510)n / k(0.0125)m (0.0255)n
                                2 = 2 power of n

Thus,n,order of rxn wrt Cl2 = 1

Rate exp3 / Rate exp1 = k[NO]exp3(m) [Cl2]exp3(n) / k[NO]exp1(m) [Cl2]exp1(n)
9.08 x10-5/2.27 x10-5 = k(0.0250)m (0.0255)n / k(0.0125)m (0.0255)n
                                  4 = 2 power of m

Thus,m, order of rxn wrt NO = 2
Thus,rate law is Rate = k [NO]2 [Cl2]
Overall order of reaction  = m+n = 2+1=3