Transcript ppt

Determining Rate Laws
2 NO(g) + O2(g)  2 NO2(g)
Determine the rate expression and the value of the rate
constant from the data below.
[NO] (mol L-1) [O2](mol L-1)
initial rate (mol L-1 s-1)
(1) 1.0 x 10-4
1.0 x 10-4
2.8 x 10-6
(2) 1.0 x 10-4
3.0 x 10-4
8.4 x 10-6
(3) 2.0 x 10-4
3.0 x 10-4
3.4 x 10-5
Rate = k [O2]m [NO]n
To determine the rate law from the data, first determine the
dependence of the rate on each reactant separately.
rate2/rate1 = k [O2]2m [NO]2n / k [O2]1m [NO]1n
8.4 x 10-6 / 2.8 x 10-6 = (3.0 x 10-4)m/ (1.0 x 10-4)m
3= 3m => m = 1; 1st order in O2
rate3/rate2 = k [O2]3m [NO]3n / k [O2]2m [NO]2n
3.4 x 10-5 / 8.4 x 10-6 = (2.0 x 10-4)n/ (1.0 x 10-4)n
4= 2n => n = 2; 2nd order in NO
Rate = k [O2][NO]2
Order of reaction = 3
2.8 x 10-6 mol L-1s-1 = k [1.0 x 10-4 mol L-1] [1.0 x 10-4 mol L-1]2
k = 2.8 x 106 L2 mol-2s-1
Concentration and Time - Integrated Rate Laws
Integrated rate laws: variation of concentration of reactants
or products at any time
Derived from the experimental rate laws
Zero order reactions
AP
- d[A]/ dt = k
d[A] = - k dt
[A]t = [A]o - k t
integrated rate law
[A]o : concentration of A at t = 0
[ A]t
 d[A]
[ A]o

t
  kdt
0
Slope = -k
First Order Reactions
Rate = - d[A]/ dt = k [A]
first order reaction
Units of k for a 1st order reaction is time-1
d[A]/ dt = - k [A]
d[A]/[A] = - k dt
Solution is:
ln [A]t = - kt
[A]o
[A]t = [A]o e-kt
[A]o where is the initial concentration of A at time t = 0
[ A]t d[A]

[ A]o A

t
  kdt
0
N2O5(g)  N2O4(g) + 1/2 O2(g)
ln[A]t = ln [A]o - k t
[A]t = [A]o e-kt
Half life of a 1st order reaction
Half life : time it takes for the concentration of the reactant A
to fall to half its initial value
t1/2 when [A]t = [A]o/2
ln[A]t = ln [A]o - kt
ln [A]o/2 = ln [A]o - k t1/2
ln(1/2) = - k t1/2
ln(2) = k t1/2
t1/2 = ln(2) / k
0.693
t1/2 =
k
Mercury (II) is eliminated from the body by a first-order
process that has a half life of 6 days. If a person accidentally
ingests mercury(II) by eating contaminated grain, what
percentage of mercury (II) would remain in the body after 30
days if therapeutic measures were not taken?
k = ln 2 / t1/2 = (ln 2) / (6 days)
Fraction remaining after 30 days
[A]t / [A]0 = e-kt = 0.03
Answer: 3% remaining in the body after 30 days.
Radioactive decay is a first order process
Nt = No e-kt
where Nt is the number of radioactive nuclei at time t
No is the initial number of radioactive nuclei
k is called the decay constant
t1/2 = ln 2/ k
Carbon-14 dating uses the decay of 14C
14
6C
0
 147N  1
e  
14C
is produced in the atmosphere at an almost constant
rate 14N  1n  14 C  1p
7
0
6
1
As a result proportion of 14C to 12C is ~ constant
14C
enters living systems as 14CO2; all living systems have a
fixed ratio of 14C to 12C; about 1 14C to 1012 12C
When the organism dies, there is no longer exchange of C
with surroundings, but 14C already in the organism
continues to decay with a constant half life, so ratio of 14C to
12C decreases.
Second order reactions
rate = k [A] [B] or rate = k [A]2
Rate = k[A]2
2nd order reaction for which the rate
depends on one reactant
- d[A]/ dt = k [A]2
d[A]/[A]2 = - k dt
1
1

 kt
[A]t [A]o
[A]t

[A]o
d[A]
2
[A]

t
 kdt
0
[A]t 
[A]o
1  [A]o kt
[A]o
[A]t 
1  [A]o kt
t1/2
1

k[A]o
The half-life of a 2nd order reaction when
[A] = [A]o/2
ln[A]t = ln [A]o - kt
1st order
1
1

 kt
[A]t [A]o
2nd order
2C2F4  C4F8
ln[C2F4] vs time - nonlinear
1
1

 kt
[A]t [A]o
slope = k
rate = k [C2F4]2
Reaction Mechanisms
Determines rate laws; use experimental rate law to determine
mechanism
Reactions often proceed in a series of steps - elementary
reactions
For example:
O2 + light  O2*
O2*  O. + O.
2(O. + O2 + M  O3 + M)
Overall reaction: 3O2 + light  2O3
O. is an intermediate species; involved in a step in the
mechanism, but does not appear in the overall reaction
Overall reaction
6 Fe2+(aq) + Cr2O72-(aq) + 14H+(aq) 
6 Fe3+(aq) + 2 Cr3+(aq) + 7 H2O(l)
The rate of an elementary reaction is directly proportional to
the product of the concentrations of the reactants, each
raised to a power equal to its coefficient in the balanced
equation for that step
The number of reacting species in an elementary reaction molecularity
Types of elementary reactions
Unimolecular reaction; molecularity = 1
O 2*  O + O
Rate = k[O2*]
Bimolecular reaction; molecularity = 2
NO(g) + O3(g)  NO2(g) + O2(g)
Rate = k [NO] [O3]
Termolecular reaction; molecularity = 3
O + O2 + M  O3 + M
rate = k [O] [O2] [M]
Termolecular reactions are low probability reactions; require
three species to come together simultaneously
From rate law to reaction mechanism
Products of a reaction can never be produced faster than the
rate of the slowest elementary reaction - rate determining
step
Experimental data for the reaction between NO2 and F2
indicate a second-order rate
Overall reaction: 2 NO2(g) + F2(g)  2FNO2(g)
Rate = k [NO2] [F2]
How can a mechanism be deduced from the rate law?
Rate law indicates that the reaction cannot take place in one
step