KINETICS (Chapter 13 – Rates of Reaction)

NOTES:
We saw from thermodynamics that we can predict with confidence the extent of a chemical reaction, i.e.,
thermodynamics can tell you if a reaction will move in the forward direction when ∆G < 0. We can also
determine whether products or reactants are favoured at equilibrium, e.g., ∆G° = – RTlnKeq. But this tells
us absolutely NOTHING about how quickly or slowly a reaction takes place. Reactions can have a very
large and negative ∆G and still take years to produce a substantial amount of products.

The study of allows you to determine:

• (how fast, slow)
• (such as concentrations & temperature)
•

– Section 13.1
• rate (i.e., speed, velocity) indicates that time is a factor to be considered.
• or something similar.
• The rate of almost all chemical reactions changes as the reaction proceeds;
they
• The ZERO ; the
.
(We shall see why this is so once we examine the rate equations for chemical processes.)
• (i.e., the sequence of molecular steps that
the reaction takes to proceed to the products).

Experimental Determination of Reaction Rates – Section 13.2

To determine a rate of reaction, we must measure ∆[ ]/∆t (or d[ ]/dt).
e.g., for the reaction: 2N2O5(in CCl4) → 4NO2(in CCl4) + O2(g),
we can follow the course of the reaction by measuring the change in [N2O5]
OR the change in [NO2] OR the change in P(O2) as the reaction proceeds.
Rate is always a _____________
POSITIVE number, therefore,

Plot of concentration versus time for the N2O5 decomposition reaction, i.e.,
2N2O5(in CCl4) → 4NO2(in CCl4) + O2(g)
Instantaneous rate slope

For a finite change in time (∆t), we

measure the AVERAGE rate of change,
e.g., average rate of change of [NO2] =
∆ [NO2] /∆t (i.e., slope = rise over run)

To find the instantaneous rate of NO2 at

time t, one has to determine the slope of
the tangent line at time, t.

111
Notes: NOTES:
a) One usually the
b) (e.g., ∆[ ]/ ∆t or d[ ]/dt).
c) Value for the r may be in the reaction,
e.g., for A + 2B → C, rate of disappearance of B is 2 × the rate of disappearance of A.
d) s must be Then we can propose a rate equation (or
rate law) which tells us about the conc’n dependence of the rate, i.e., rate α concentration.
e) gives a (the ).
f) A mechanism is a that hopes to ,
i.e., the molecular level reorganization.
reactants: x(-1) and products: x(+1)
Look at the equation: 2N2O5 → 4NO2 + O2
At any time, t, the rate of the reaction is given by:
Rate = – ½ × ∆[N2O5 ]/∆t = + ¼ × d[NO2]/dt = + ∆[O2]/∆t

Rate = –(1/a) ∆ [A]/∆

∆t = –(1/b) d[B]/dt = (1/c) ∆ [C]/∆
∆ t = (1/d) d[D]/dt
Note: Merely by looking at a balanced equation and knowing nothing about the
mechanism. etc., you can write down this "rate" statement.
When the rate relationship includes reactants, because their concentrations are decreasing
we need to include a negative sign to cancel out this effect. This will make the rate positive
(remember it is always positive!). In the case of products, their concentrations are
increasing so we don’t have to include the negative sign.

Clicker Question#1: All the following would be expected to affect the rate of a
chemical reaction EXCEPT
A) increasing reactant concentrations. the rate of rxn depends
on the conc’ns and states
of the reactants,
C) increasing the temperature. temperature, and
D) changing the solvent. presence of a catalyst

E) adding a catalyst. Activation energy is lowered, allowing rxn to occur more readily

Rate Law – Section 13.3

• the of a chemical reaction (or current)

Rates are often proportional to the concentration of 1 or 2 reactants with each reactant raised
to a small integral power. Generally, for the reaction:
aA + bB → cC + dD
(this relationship is known as the “Rate law”)

The reaction is then x order with respect to A, and y order with respect to B.
The overall order is the sum of the various orders, i.e., x + y

112
 • RATE CONSTANT
the proportionality constant “k” is called the _______________________ . NOTES:
•

•
• The "order" of a chemical reaction is the number of chemical concentration
terms upon which the rate depends.

(e.g., 2N2O5(g) → 4NO2(g) + O2(g); Rate = k[N2O5])

Case I is an example of a rate expression.
The rate of the reaction depends upon one concentration term.

(e.g., 2NO2 → 2NO + O2 ; Rate = k[NO2]2)

Case II is an example of a rate expression.
The rate depends upon two concentration terms.

(e.g., H2 + I2 → 2HI; Rate = k[H2][I2])

Cases III is an example of rate expression.
The rate depends upon two concentration terms.

(e.g., C2H5OH → CH3CHO; Rate = constant)

Case IV is an example of a rate expression.

(e.g., CH3CHO → CH4 + CO; Rate = k[CH3CHO]1.5)

Case V is an example of a rate expression.
The rate depends upon one & a half concentration terms.
Note:
a)
b) Order is only
c) Orders may be (not common) or even (not common).
d) Reaction rate
e) – independent of concentration (see case IV).
f) 3rd order – rare.

Method for Determining Kinetic Order

• study how the rate changes with different concentrations of reactants
• if reaction is 1st order, rate will ______________
DOUBLE if initial concentration of Direct relationship
substance doubles.
2^x = 4, exponential
• if reaction is 2nd order, rate will quadruple when concentration is DOUBLED
__________ relationship

113
For the reaction: 2N2O5(in CCl4) → 4NO 2(in CCl4) + O 2(g) NOTES:

1st
i.e., first-order in N2O5 and ________order overall.
−∆[𝑁𝑁2 𝑂𝑂5 ] ∆[𝑁𝑁𝑂𝑂2] ∆[𝑂𝑂2]
i.e., Rate = = = = k[N2O5]
2 ×∆𝑡𝑡 4×∆𝑡𝑡 ∆𝑡𝑡

For the reaction: NO(g) + CO(g) → CO2(g) + ½N2(g) Dependent on both the
reactants ; b/c order is
BY EXPERIMENT it is found that Rate = k[NO][CO] changing, units of K also
2nd
i.e., first-order in NO, first-order in CO and ____________order overall. changes

Clicker Question#2: For the reaction, IO3–(aq) + 5I–(aq) + 6H+(aq) → 3I2(aq) + 3H2O(l),
the rate of disappearance of I – at a particular time and concentration is
5.0 × 10–3 M s–1. What is the rate of appearance of I 2 in M/sec?
A) –5.0 × 10–3 M s–1 Rate = - [I-] / (5*∆t) = ∆[I2] / (3*∆t)
B) 1.0 × 10–3 M s–1 = (1/5) (5 x 10^-3)
= ∆[I2] / (3*∆t)
D) 5.0 × 10–3 M s–1
E) 6.0 × 10–3 M s–1 Therefore, ∆[I2] / ∆t = 3 x 10^-3 M s

The distinction b/w a rate & a rate constant is a frequent point of confusion. Units are helpful here.

A rate is in , e.g., M.s–1.

Rate constants are the proportionality constants between the rate and the
concentration terms in the rate expression and therefore have DIFFERENT units
according to the order of the reaction.
A rate constant is a characteristic property of the reaction under discussion; it is
called a to remind us that, in contrast with the reaction rate,
of substances reacting.
; they almost always increase with increasing temperature.

NOTE: , i.e., mol L–1 s–1.

For a first-order rate equation: Rate (mol L–1 s–1) = k[A],
s^-1
the units of the rate constant, k, must be _________.

For a second-order rate equation: Rate (mol L–1 s–1) = k[A]2,

the units for k must be ____________________
L / mol•s

A useful method for determining the kinetic order of a reaction experimentally is to study how the
rate changes with different concentrations of the reactants (i.e., Kinetics Wet Lab).
For zero-order, k will be mols/L•s ; k will have units of conc’n/time
114
Experimental Determination of RATE LAW (Method of Initial Rates) NOTES:
To determine the rate law (i.e., Rate = k[A]x [B]y [C]z) we need to do some
experiments. For example, take data in the early stages of a reaction (called the
method of initial rates), and determine values for x, y, z and k.
e.g., , where [ ]0 represents initial concentrations.

A systematic variation of the concentrations of reactants is usually used in

order to determine the order of a reaction. Remember the process is:

e.g., A → B; Rate0 = k[A] 0x

Value of x (rxn order) Effect on rate when [A]0 is doubled (1M → 2M)
0 [1]0 → [2]0 = 1, no effect on rate
½ [1]½ → [2] ½ = 1.41, rate increased by 1.41
1 [1]1 → [2]1 = 2, rate increased by 2 (doubles)
2 [1]2 → [2]2 = 4, rate increased by 4 (quadruples)

EXAMPLE #1: A + B → 2 P; Rate0 = k[A]0x[B]0y x = 0, y = 1

Expt. Initial Rate [A] 0 [B]0
# (mol L-1 h-1) If you have something with
-2 the exponent to zero, it does
1 0.5 × 10
nothing
2 0.5 × 10-2 0.75
3 0.5 × 10-2 1.00
4 1.0 × 10-2 0.40
5 1.5 × 10-2 0.60

a) In the first three experiments, [B]0 is constant and [A]0 changes, but the rate
does not change, i.e., rate is independent of [A]0 & ∴ ________
zero order in [A]

b) In experiments 1, 4 and 5, [A]0 kept constant while [B]0 changes.

1st
Change in rate directly proportional to the change in [B]0; therefore, _______
order in [B]
∴ k[A]00[B]01 = overall first order in [B].

Can get k from the data:

= 1.5×10-2 mol L-1 h-1/0.60 mol L-1 = 2.5×10-2 h-1

115
 EXAMPLE #2: NOTES:
In the gas–phase reaction at 25°C: 2 NO + O2 → 2 NO2
[NO] [O2 ] Initial Rate
Expt. (mmol⋅L –1) (mmol⋅L–1 ) (µ mol⋅L–1⋅s –1 )
1 0.28 1.44 0.69
2 0.84 1.44 6.2
3 2.52 1.44 56.
4 0.84 0.36 1.6
Note: Watch units!

Table entries 1, 2, and 3 are run at constant [O 2], and can be used to determine the order
with respect to NO. Table entries 2 and 4 are run at constant NO, and can be used to
determine the order with respect to O2.
The rate expression will be: rate = k [NO]m [O2]n and we want to find the values of the
constants m and n. Compare the ratios of the rates with the ratios of concentrations.
Comparing table entries 1 and 2 at constant [O2]:
[k(0.84)^m * (1.44)^n] = 6.2 / [k(0.28)^m * (1.44)^n] = 0.69
Rate(2)
Rate(1)
=
(0.84/0.28)^m = (6.2 / 0.69)
3^m = 8.99
m log3 = log 8.99
m=2
Since increasing [NO] by three increases the rate by nine, it is likely that the reaction is
2nd
__________-order in NO. (Check that this relationship is also true for table entries 2 & 3).
Now compare table entries 2 and 4, at constant [NO].
Rate(2)
Rate(4)
= [k(0.84)^m * (1.44)^n] = 6.2 / [k(0.84)^m * (0.36)^n] = 1.6
(1.44/0.36)^n = (6.2/1.6)
4^n = 3.88 (APPROX 4)
n=1

Since increasing [O2] by four increases the rate by four , it is likely that the reaction is
1st
_________-order in O2. Thus the rate equation is: Rate = k [NO] 2[O2] .

What is the value of the rate constant k and what are the units of k?
If we want to find the rate constant in terms of mol/L or M, and seconds, we need to
convert the units. Using experiment#1:
Rate = 0.69 µ mol L–1 s–1 × (1 mol/1 × 106 µ mol) = 6.9 × 10–7 mol L–1 s–1
[NO] = 0.28 mmol L–1 × (1 mol/1 × 103 mmol) = 2.8 × 10–4 mol L–1
[O2] = 1.44 mmol L–1 × (1 mol/1 × 103 mmol) = _______________
1.44 x 10^-3 mol L–1

[6.9 x 10^-7 mol / L • s] / [(2.8 x 10^-4 mol/L)^2 * 1.44 x 10^-3 mol/L]

6.1 x 10^3 / M^2 • s

k = ____________________ for this 3rd order reaction!
i.e., the rate law for this process is:
Rate = 6.1 × 103 M–2 s–1 [NO]2 [O2] or simply .
116

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 Question A: The hypochlorite ion oxidizes the iodide ion in aqueous sol’n as NOTES:
represented by OCl– + I– → OI– + Cl–. The rate of formation of OI– is given by:
- -
[I ][OCl ] Rate = []^1 []^1 []^-1
Hydroxide is the catalyst Rate = k -
[OH ]
The overall reaction order and the order with respect to OH– are Therefore, Overall
Order = 1+1-1 = 1
A) 0 & 1 B) 0 & –1 D) 2 & 1 E) 2 & –1.

Question B: If the rate law for a reaction is Rate = k[ClO3–][I–][H+]2, what are the Rate = [] / time
units of k when time is in seconds and concentration is in moles per liter? = K[]^4
mol L ⋅s mol 2 L2 3
A) B) C) 2 D)
L⋅s mol L ⋅s mol 2 ⋅ s

Problem 1 – try on your own…

A reaction between gaseous substances A and B yielded the following set of data:
Expt. # Initial [A] Initial [B] Initial rate
(mol L–1) (mol L–1) (mol L–1 min–1)
1 1.00 0.25 0.26
2 1.00 0.50 0.52
3 1.00 1.00 β
4 2.00 1.00 4.16
5 3.00 1.00 9.36
6 4.00 α 16.64

Deduce (and show your reasoning clearly) the values of α and β in the above table
and of k, m and n in the rate expression: rate = k[A]m[B]n.

Problem 2 – try on your own…

The rxn: 2H2O2(aq) → 2H2O(aq) + O2(g) is catalyzed by I– (aq) and by H+(aq).
The following data were obtained: (conc. in mol/litre, rates in mol⋅litre-1⋅second-1)
Expt # [H2O2] [I–] [H+] Initial Rate (M/sec)
1 0.20 0.010 0.010 2.0 × 10–3
2 0.40 0.010 0.0฀0 4.0 × 10–3
3 0.40 0฀020 0.010 8.0 × 10–3
4 0.20 0.020 0.020 1.6 × 10–2
5 0.40 0.020 0.040 δ
What are: (i) m, n, p in the rate law equation: rate = k [H2O2]m [I–]n [H+]p ?
(ii) the value and units of k ?
(iii) the value of δ

117
Answer 1: Rate = k[A]m [B] n To find m, compare 4 & 5 when [B] is constant: NOTES:
Expt #4: 4.16 = k (2.00)m (1.00)n = (2.00)m
Expt #5: 9.36 = k (3.00)m (1.00)n = (3.00)m
0.44 = 0.66 m
log 0.44 = m log 0.66
m = log 0.44 / log 0.66; ∴m ≈ 2

To find n, compare 1 & 2 when [A] is constant:

Expt #1: 0.26 = k (1.00)x (0.25)n = (0.25)n ∴n≈1
Expt #2: 0.52 = k (1.00)x (0.50)n = (0.50)n
∴ Rate Law: rate = k[A] [B]
2 1

To find the rate constant, use any of the experimental runs:

i.e., k = rate/[A]2 [B]1 = 0.26 / (1.00) 2 (0.25) = 1.04 M–2min–1

To determine β , use experimental runs 2 & 3. If the [B] is doubled, the rate
doubles. Therefore β = 1.04 M min–1
To determine α , compare runs 5 & 6:
Expt #5: 9.36 = k (3.00)2 (1.00) = 9 ∴ α ≈ 1.00
Expt #6: 16.64 = k (4.00)2 (α ) 16α

Answer 2: Rate = k [H2O2]m [I–]n [H+]p

To find m, compare 1 & 2 when [I–] and [H+] are constant:
Expt #1: 2.0 × 10–3 = k (0.20)m (0.010)n (0.010)p ∴m=1
Expt #2: 4.0 × 10–3 = k (0.40)m (0.010)n (0.010)p

To determine n, compare 2 & 3:

Expt #2: 4.0 × 10–3 = k (0.40)m (0.010)n (0.010)p ∴n=1
Expt #3: 8.0 × 10–3 = k (0.40)m (0.020)n (0.010)p

To determine p, compare 3&4 and use m = 1:

Expt #3: 8.0 × 10–3 = k (0.40) (0.020)n (0.010)p
Expt #4: 1.6 × 10–2 = k (0.20) (0.020)n (0.020)p
0.5 = 2 × 0.5 p
0.25 = 0.5 p
p =2
∴ Rate Law: rate = k [H2O2] [I–] [H+]2 (overall order = 4)
To solve for k: k = rate / [H2O2] [I–] [H+]2
k = 2.0 ×10–3/(0.20)(0.010)(0.010)2
k = 1.0 × 104 M–3s–1
To find δ , compare 3 & 5:
Expt #3: 8.0 × 10–3 = k (0.40) (0.020) (0.010)2 = 0.010 δ = 0.128
Expt #5: δ k (0.40) (0.020) (0.040)2 0.160

118
 NOTES:
Integrated Rate Laws – dependence of concentration on time – Section 13.4
We often want a mathematical relationship showing how a reactant concentration changes over time.
We use calculus to convert the differential rate equations into integrated rate equations.
This serves a couple of purposes:
a) By examining how the conc’n changes with time during a single exp’t; we can determine
the rate law. [Note: the initial rate law method needs several exp’ts.]
b) We can determine how long a rxn must proceed to give a particular conc’n.
c) We can determine what the concentrations are after a period of time.

An integrated rate law is a formula that gives the (or

products) after the start of the reaction, if the initial concentration of
reactants is known.

–∆[A]/∆t = ∴ rate is independent of concentration

Units? M/s

Example: 2NH3(g) → N2(g) + 3H2(g)

Zero-order reactions continue at the same rate until all reactants gone, then the rate
stops abruptly.

Zero-Order Derivation:
Rate = –d[A]/dt = k This is the differential form of the rate law.

Isolate the variables, [A] and t, and integrate each side between
the limits of [A]0 to [A]t and t ime 0 to t, i.e., Text
t
[A ]t
∫[ A]0
d [ A] = − k ∫ dt
0

Integrating with respect to [A] on the left-hand side, we get [A] (i.e., ∫ dx = x).
Integrating with respect to t on the right-hand side gives t. So we get:
[A ] t
[ A] [A ]t = − kt 0
0

[A]t – [A]0 = –k(t – 0)

OR
This is the integrated form of the rate law where [A]t is the conc’n at some time, t.

119
 NOTES:
Absorbance and
If it doesn’t follow the straight line, concentration are
then it’s one of the other orders statiscally directly
propotional

Might encounter
encou something
ing like this
Zero Order Rate Example:
Clearance of alcohol from the body after consumption is a zero-order process with a
rate constant 0.20 ounces per hour. Beer is typically sold in 10 oz. bottles with a 5%
alcohol content, so if you drink 1 bottle of beer, you have consumed: 10 oz. × 0.05 =
0.50 oz. of alcohol.
(a) If 5 (10 oz.) beers are consumed, how long before no alcohol is left in the body?
(b) If the legal limit of blood alcohol was equivalent to 1 beer, how long after
consuming 5 beers would it be "safe" to drive?

Answer: A rate constant, k, of 0.20 ounces per hour ≅ 5 hours per ounce (oz.).
Alcohol consumed = 5 beers × 0.05 oz. of alcohol/ beer = 2.5 oz.

where [A]0 = 2.5 oz. & [A] = 0 oz.

∴ 0 = 2.5 oz. – (0.20 oz./hr × t hr )
t = 2.5 oz. / 0.20 oz./hr = 13 hours

(b) 1 beer has 0.50 oz. alcohol, so again use:

, only now .
0.50 oz. = 2.5 oz. – (0.20 oz./hr × t hr )
t = (2.5 – 0.50)/0.20 = 10 hours

120
 Reaction rate = k[A] or NOTES:
[ A ]t t
d[ A]
Integrated rate law: ∫[A ] [A ] = − ∫0 kdt ; ∴ln[A]t – ln[A]0 = – kt OR
0

ln[A]t =– kt + ln[A]0 (integrated first-order rate law)

(i.e., y = mx + b)

 [A ]   [A ] 
ln 
 [A ]  = – kt
ln 
 [ A ]  = kt
t 0
OR OR
 0   t 

OR
First order rate constants have the units of (time)–1.

A plot of the logarithm of the concentration of A remaining versus time gives –k for
the slope and ln[A]0 as the y-intercept, i.e.,
ln [A] ln[A] = –kt + ln[A] 0
(y = mx + b)

ln [A]0

slope = –k

The of any reaction is the

so that
[ A] 0
Substitute [A]t = into the 1st-order equation and solve to t:
2
 
 [ A ]0 
ln   = ln(2) = k t ½
 [ A ]0 
 2 
(first-order half-life)
Note: Half–life for a first order reaction is

, i.e.,

( Final Activity ) = e–kt or [ A ]t

= e–kt (more later…)
( Initial Activity ) [ A]0

121
First Order Example 1 NOTES:
A reaction A → B is first order in A and first-order overall. It requires 60.0 min
1st order: Rate = k[A]
for 75.0% of A to react. The rate constant for this process in units of min–1 is:
A) 4.79 × 10–3 It matters on how much is left, not how much has gone,
B) 1.00 × 10–3 therefore 25% is left; [A] / [A]0 = 0.25
C) 1.16 × 10–2 Integrated rate law:
D) 1.73 × 10–2 ln([A] / [A]0) = -kt
ln(0.25) = -k(60.0 mins)
k = 2.31 x 10^-2 /mins

Answer:
First-order: Rate =
At 60 minutes, 75% of A has reacted. What is [A]/[A]0?

First Order Rate Example 2

For the 1st-order decomposition of N2O5 at a given temperature, it was found that
[N2O5] was 0.0300 mol⋅L–1 after 10.0 min and 0.0150 mol⋅L–1 after 30.0 min. 1 way to approach
Calculate the rate constant k and the original N2O5 concentration when the reaction
was started.

Answer: After 20.0 minutes, how much N2O5 has reacted?

k = ln(2) / t(1/2)
= 0.693 / 20.0 min
= 0.0347 / min
Another way to
data with a 1st-order plot (where you should get a very good straight line!), i.e., approach
Time, min [N2O5], M ln[N2O5]
10.0 0.0300 -3.507
30.0 0.0150 -4.200 m = -0.0347 / min
Because this is a first-order reaction, the slope of the line is equal to –k. (You can use
the statistical function on your calculator to do "linear regression" and solve for the slope of the line.)

To solve for [A]0, use ln[A]0 = kt + ln[A] and sub in one set of the values, i.e.,
ln[A]0 = [(0.0347 / min) * 10.0 min] _ ln(0.030)
[A]0 = 0.0424 M

122
First Order Rate Example 3 - Radioactive Decay NOTES:
A piece of wood, found in an archeological dig, has a carbon–14 activity that is 90% Don’t need to know
of the current carbon–14 activity. How old is the piece of wood? (t ½ for carbon–14 [A]o for 1st order
= 5.73 × 103 years) rate examples.
Answer: Radioactivity follows 1st-order kinetics, ∴ using the 1st-order half–life:
In first order, rate is
k = ln 2/t½ = 0.693/5.73 × 103 years = 1.21 x 10^-4 / years
NOT dependent on
Use (Final Activity)/(Initial Activity) = e–kt temperature
90% of the current activity makes the ratio of [A]/[A]0 = 0.90
0.90 = e–(0.000121)t
ln 0.90 = 0.000121 t
t = 870 years

Rate law:
or
[ A]t t
d [A] d[ A]
[A]
2
= – k dt i.e., ∫
[ A ]0
[ A]2
= −∫ kdt
0

–
[ ] [ ]
The second order rate constant has the units L⋅mol–1⋅s–1 or M–1⋅s–1.

Plot for Second-Order Kinetics:

1/[A] 1/[A] = 1/[A]0 + kt
(y = b + mx)

slope = +k
1/[A] 0
t

1/[A] versus time gives a straight line with a slope = +k.

]
Unlike a first order reaction, a second-order reaction
; if the initial concentration of reactant is higher, the reaction
is not only faster in terms of moles of reactant consumed per litre per second but the half–
life is shorter as well. This makes the concept of half-life far less useful for second-order
than for a first-order reaction where the half-life is a consistent value.
123
Second Order Rate Example NOTES:
The decomposition reaction: 2A → 3B is 2nd order. At t = 0, [A] = 0.60 mol L–1
(a) Calculate rate constant for this rxn if the initial rate is 10 mol L–1 s–1 at 25°C.
(b) How much time is need to form 0.30 mol L–1 of B?

Answer: Second order: Rate = k[A]^2

(a) k = Rate/[A]2 = (10 mol L–1 s–1)/( 0.60 mol L–1 ) 2 = 28 /M•s

(b) Based on the stoichiometry of the chemical equation, to form 0.30 M of B, we

must consume how much of A, i.e.,
2 mol A
0.30 mol B × = 0.2 mol A.
3 mol B
Therefore, 0.60 M – 0.20 M = 0.40 M of A must remain.
Using the integrated rate law for a simple second order:
1/[A]t - 1/[A]0 = kt
1/0.40 - 1/0.60 = 28t
t = 0.03 seconds

KINETICS PROBLEMS
Problem 1: The rate equation for the rxn: A → B + C is expressed in terms of [A]
only. The rate of disappearance of A is 8.0 mmol L–1 s–1 when [A] = 0.20 mol L–1.
Calculate the value of the rate constant k if the rxn is (a) 1st-order, (b) 2nd-order.

Problem 2
For the decomposition of CH2N2 at 600°C, the following data were obtained:
t (min) [CH2N2] ln[ ] 1/[ ]
0 0.100 –2.30 10.0
5 0.076 –2.58 13.2
10 0.058 –2.85 17.2
15 0.044 –3.12 22.7
20 0.033 –3.41 30.0
25 0.025 –3.69 40.0

Use Graphical methods to determine the ORDER of the reaction and determine the rate
constant from the SLOPE of your plot. You may wish to use the Kinetics Plotting Tool:
[Link]/educmat/chm19105/kinetics/intro_kinetic_applet.htm
WARNING: Applet simply calculates slope based on 1st and last data point; not from line of best fit!

124
Problem 3
The half–life of a reaction: A → products is 12.0 minutes when the initial value of
[A] is 0.100 M. How long will it take for [A] to drop to 0.020 M if the reaction is
(a) 1st -order, or (b) 2nd -order?

Problem 4: More Difficult Rate Law Question

Beginning with equal concentrations of A and B, the rate was found to decrease to
40.7% of its initial value after 19.0% of A had been consumed. After 31.0%
consumption of A, the rate had decreased to 18.1% of its initial value. Determine
the rate law for the reaction: A + 2B → C + D.

Answer 1:
Rate = 8.0 mmol L–1 s–1 × 1 mol/1000 mmol = 8.0 × 10–3 mol L–1 s–1
(a) First-Order: Rate = k[A]
k = 8.0 × 10–3 mol L–1 s–1/0.20 mol/L = 0.04 s–1

(b) Second-Order: Rate = k[A]2

k = 8.0 × 10–3 mol L–1 s–1/{0.20 mol/L}2 = 0.2 M–1 s–1

Answer 2:
If first-order, a plot of ln[A] versus time will result in a straight line and slope = –k.
If second-order, a plot of 1/[A] versus time results in a straight line and slope = k.
If zero-order, a plot of [A] versus time gives a straight line and a slope = –k.
In this case, the first case is true and the slope of the line is –0.056
(∴ k = 0.056 min–1).
Answer 3:
(a) First-order half-life: k = 0.693/12.0 = 0.0578 min–1
ln[A]0 – ln[A] = kt
t = {ln[A]0 – ln[A]}/k = {ln(0.100) – ln(0.020)}/0.0578
t = 27.8 minutes
(b) Second-order half-life: k = 1/{12.0 × 0.100} = 0.833 M–1 min–1
1/[A] – 1/[A]0 = kt
t = {1/0.020 – 1/0.100}/0.833
t = 48.0 minutes
Answer 4:
Relationship % consumpt’n of A [A] [B] Rate
1 0% Let [A] 0 = x Let [B] 0 = x Let R 0= Initial Rate
2 19% (1 – 0.19)x (1–{2 × 0.19})x 0.407R 0
= 0.81x = 0.62x
3 31% (1–0.31)x (1–{2 × 0.31})x 0.181R 0
= 0.69x = 0.38x

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Based on the general rate law: Rate = k[A]m [B]n, equations can be derived:
From Relationship #1: R0 = k x m x n = kx m+n
From #2: 0.407R0 = k{0.81x}m {0.62x}n = k 0.81m 0.62n x m+n
From #3: 0.181R0 = k{0.69x}m {0.38x}n = k0.69m 0.38n x m+n
Divide equation #2 and #3 by #1 to get two simultaneous equations to solve:
(2a) 0.407 = 0.81m 0.62 n
(3a) 0.181 = 0.69m 0.38 n
where m = 2 and n =1 to give: Rate = k[A]2[B]
*************************************************************************
Algebra for solving for m and n:
Simplify using logarithm rules: (2b) log 0.407 = m log {0.81} + n log{ 0.62}
(3b) log 0.181= m log {0.69} + n log {0.38}
To get: (2c) -0.39 = -0.09m – 0.21n
(3c) -0.74 = -0.16m – 0.42n
Isolate for m (i.e., 2c × 2): (2d) -0.78 = -0.18m – 0.42n
(3d) -0.74 = -0.16m – 0.42n
(2d) – (3d): –0.04 = –0.02m; m = 2
Solve for n, e.g., (2d) –0.78 = –0.18(2) – 0.42n; n =1

Additional Problems:
1. Based on 2H2S(g) + O2(g) → 2S(s) + 2H2O(g), we can conclude that
A) the reaction is second order in H2S and first order in O2.
B) the reaction is first order in H2S and second order in O2.
C) Rate = k[H2S]2[O2].
D) Rate = k[H2S][O2].
E) None of these conclusions are justified.

2. The magnitude of the rate constant k is dependent on the

A) concentration of the reactant. B) concentration of the product.
C) temperature. D) order of the reaction.

3. Consider these data in order to answer the question that follows:

[A] [B] [C] Initial Rate (Ms–1)
A) Zero order
0.4 0.4 0.2 160
B) First order
0.2 0.4 0.4 80 C) Second order
0.6 0.1 0.2 15
D) Minus one (rate ∝ 1/B)
0.2 0.1 0.2 5
E) Impossible to tell from the data given.
0.2 0.2 0.4 20

Wh t i th d f th ti ith t t C?

126
4. i) Which order has a half-life that depends upon 1/k?
A) Zero order
B) First order
C) Second order
D) All of the above
ii) Which order has a half-life that only depends upon 1/k and no other variable?

5. Nitrosyl chloride is produced from the reaction of nitrogen monoxide and chlorine.
2NO(g) + Cl2(g) → 2NOCl(g)
The following initial rates at a given temperature were obtained for the conc’ns listed below:
Experiment  mol   mol   mol 
NO   Cl 2   Rate  
 L   L   L • hr 
1 0.25 0.25 2.21
2 0.50 0.25 8.83
3 0.50 0.50 17.5

The experimental rate law is

A) rate = k[NO].
B) rate = k[NO]1/2[Cl2].
C) rate = k[NO][Cl2]1/2.
D) rate = k[NO]2[Cl2].
E) rate = k[NO][Cl2].

6. For a first-order rxn: aA → products, the first half-life is 20 minutes. The second half-life is
A) 10 minutes. B) 20 minutes. C) 40 minutes.

7. At a particular temperature the half-life of a zero-order reaction is 20.0 minutes. How long
will it take for the reactant concentration to be depleted by a factor of eight?
A) 20.0 minutes
B) 35.0 minutes
C) 60.0 minutes
D) 140. minutes
E) 160. minutes

Answers: 1. E; 2. C; 3. A; 4 i) D; 4 ii) B; 5. D; 6. C; 7. t½ = [A]0/2k and [A]0 = 40 k, ∴B.

127
 DEPENDENCE OF RATE ON TEMPERATURE
Experimentally it is found that for most reactions, the reaction rate NOTES:
( / decreases ) as the temperature is raised.
we rate constants at 2
By trying various combinations of plots, it was soon realised that a plot of ln k vs. diff temps to work
1/T (or logk versus 1/T) gave a linear plot with a negative slope. What does it mean backwards and find
if a plot of ln(something) plotted against 1/T gives a negative slope? What sort of activation energies
algebraic equation does this imply?
Arrhenius supplied the answer in 1899:

where k = rate constant, A = pre-exponential factor (a constant) & Ea = Activation Energy

If you take the natural logarithm of this equation:

i.e., a plot of ln k vs. 1/T gives a linear plot with intercept ln A,

with negative slope = – Ea/R,.
(where have you seen this sort of equation before?)

The Arrhenius equation allows us to do is to calculate the Activation Energy for a

reaction if we know the rate constants for the reaction at two temperatures.
Thus:
E 1
(1) at T2: ln k2 = ln A – � a � � �
R 𝑇𝑇 2
Ea 1
(2) at T1: ln k1 = ln A – � � � �
R 𝑇𝑇1

k2 E 1 1
Subtract equation (1) from (2): ln � � = – � �a � − �
𝑘𝑘1 R 𝑇𝑇2 𝑇𝑇1

k2 E 𝑇𝑇 −𝑇𝑇
By rearranging the equation: ln � � = – � a� � 𝑇𝑇1 ×𝑇𝑇2 �
𝑘𝑘1 R 1 2

OR

K2 ∆𝐻𝐻 ∆𝑇𝑇
{Recall ln� � = �R � �𝑇𝑇 𝑇𝑇 � – van’t Hoff equation}
𝐾𝐾1 1 2

The activation energy, E a is the energy that the reactants need to make the reaction
"go". The significance of the temperature, T, is that an increase in temperature
increases the average velocities and hence kinetic energies of molecules. The larger
the value of Ea, the more sensitive is the rate constant k to temperature changes.

128
 NOTES:

Reference J. Olmsted & G.M. Williams, Chemistry, 3rd ed., John

Wiley & Sons, Inc., New York, 2002, p. 682.

We can create plots to show the relationship of Ea and ∆HRxn – the reaction profile.
These plots display the difference in energy between the reactants and the products
(i.e., ∆HRxn ) and the energy changes as reactants go to products.
AB≠

A+B

Reference: L. Jones & P. Atkins, Chemistry - Molecules, Matter and

Change, 4th ed., W.H. Freeman and Company, New York, 2000, p. 592

QUESTION:
In the diagram provided, the quantity y is:
A) ∆H = z E(a) forward
B) Ea(forward) = x E(a) reversed
=y
D) collision energy
E) steric factor (p) = ∆H

129
 Collision Theory NOTES:

In collision theory, the potential energy ( / decreases ) as reactants

approach each other, reaching a maximum as the molecules distort into what is
known as a transition state or activated complex. The energy then
( increases / ) as the atoms rearrange into the bonding pattern of the
product(s). The reaction profile indicates this increase in energy due to the transition
state, located at the peak of the profile. The energy difference between the top of the
curve and the reactants represents the Ea for the reaction. Only molecules with
sufficient energy ( ) can cross the energy barrier and .

Catalysts
Catalysts ( / decrease ) the rate of reaction without being consumed in the
reaction. The catalyst provides an alternate reaction pathway which requires less
energy, i.e., Ea (with catalyst) < Ea (no catalyst).

Question 1
A reaction has an activation energy of 48 kJ mol–1 at 25°C. A catalyst increases the
rate of reaction by a factor of 1000. What is activation energy in the presence of the
catalyst, assuming the Arrhenius A–factor is unchanged?

Solution:
– Ea ( catalyst)
k catalyst [ A ]
[ B]
m n
Rate ( catalyst) Ae RT
1000
= = =
Rate ( no catalyst ) k no catalyst [A ] [B ]nm –E a ( no catalyst )
RT 1
Ae
– Ea (catalyst )
k catalyst e 1000 RT
∴ = =
– E a ( no catalyst )
k no catalyst RT 1
e
−Ea (catalyst )
 
e RT
ln  − Ea ( no catalyst)  = ln (1000 )
 
e
RT

E a (catalyst ) E a (no catalyst )
− + = ln (1000)
RT RT
Ea ( no catalyst ) − Ea ( catalyst ) = RT ln (1000 )
∴ Ea ( catalyst ) = Ea ( no catalyst ) − RT ln (1000 )
Substituting values:
Ea ( catalyst) = 48 kJ/mol − (8.314 ×10−3 kJ ⋅mol−1 ⋅ K−1 )(298.15 K) (6.9078 )
Ea catalyst = 31 kJ/mol
( )

130
Question 2 NOTES:
The reaction A → B is 1st order in A. At 25°C, 10.1% reacts in 20.0 minutes. If
Ea = 84.5 kJ mol–1, what percentage of A will react during the same period at 50°C?

Solution:
If 10.1% of A reacts, then what % remains? 100-10.1 = 89.9% left
Using the 1st–order integrated rate law, one can find k at 25°C (i.e., 5.32 × 10–3 min–1).
ln([A]/[A]) = -kt
ln(0.899) = -k(20.0mins)
k= 5.32 e-3 / min
There are now two ways of solving this problem:
– Ea
Method I: Use k = Ae RT to determine A using k1, Ea and T = 298K.
Then solve for the new rate constant (k2) at the new temperature (50°C).

 k 2  Ea  T2 – T1  to find k2 at 323K (50°C)

Method II: Use: ln =  
 k1  R  T1 × T2  when k1 = 5.32 × 10–3 min–1 at 298K
METHOD II is a
ln(K2/ (5.32 e-3/min)) = (84.5 / 8.314e-3) (25 / 298 *323)
more direct route
k2/5.32e-3/min = e^2.640
= 14.010
(k2 = 0.0745 min–1)
k2 = 0.0745 / min
Now that the new rate constant is known, the %A that has reacted at 50°C within the same
amount of time can be determined.

(Ans: 77.5%)

Question 3
At an altitude of 3000 metres on a mountain, water boils at 90°C and it takes 300
minutes to cook a "three–minute–egg". Calculate the activation energy for the
coagulation of egg–albumin = denaturing a protein. [Hint: The rate constant is inversely
proportional to cooking time.]

Solution:
At 3000 m, water boils at 90°C (T1 = 363 K) & t = 300 min. OR k1 = 1/300 = 3.33×10–3 min–1
At "sea level", water boils at 100°C (T2 = 373K) and t = 3 minutes OR k2 =
 k 2  Ea  T 2 – T1 
Use ln  =  
 k1  R  T1 × T2 

(Ans : Ea = 520 kJ/mol)

131
 Collision Theory of Gas Phase Bimolecular Reactions NOTES:
Consider the gas phase bimolecular elementary rxn: A(g) + B(g) → C(g) + D(g)
rate = – ∆[A]/∆t = – ∆[B]/∆t = k[A][B]
rate of frequency of
collide
Assumption 1: A and B must ______________ to react. collisions
-1 -1
The rate is proportional to the frequency of collisions per litre (e.g., collisions L ⋅s ).
The frequency of collisions, Z, can be calculated from the average velocity of A and B
(from the Kinetic Theory of Gases) and their cross-sectional areas.
This frequency is proportional to [A] and [B], i.e. , moles of collisions between A and B
per litre per second = Z[A][B], where Z = moles of collisions L-1⋅s-1 when [A]=[B]=1 M.

rate fraction of collisions

Assumption 2: A and B collide with an energy ( less ) than some minimum
having energy > E
value to result in a reaction.
The rate is proportional to f, the fraction of collisions having energy greater than some
value E that depends on the reaction. For gases at STP (1 atm, 273 K), the molar volume
is 22.4 L. Therefore, the concentration is 1 mole/22.4 L. There are typically around 10 8
moles of collisions L-1⋅s-1. If every collision resulted in a reaction, the initial rate would
be ~108 mol⋅L-1⋅s-1 and the reaction would be 99.9% complete in around 10-7 s.
Obviously, only a small fraction of the collisions can lead to product(s) in most
reactions. Z increases with temperature (i.e., Z ∝ T0.5).
.

For example, if E = 100 kJ/mol, then the fraction of collisions at 298 K is

f = e −E RT = exp{–100,000 J/mol/(8.314 J⋅mol-1⋅K-1 × 298 K)}
f = 3.0 × 10-18
Note: This fraction increases sharply with T and is the main reason that k increas es with T.

orientation
Assumption 3: Only collisions having the proper ___________ of the two reactants
can result in a reaction.
Rate is proportional to the fraction of the collisions having the proper orientation (p).

Putting all these assumptions together, we get: rate = k[A][B] = p × Z[A][B] × f

where, p is the fraction of collisions having the proper orientation for reaction;
Z[A][B] is the moles of collisions L-1 s-1
f = e-E/RT ≥ E
i.e., rate/([A][B]) = k = p × Z × e-E/RT

Now cast your mind back to the Arrhenius Equation:

k = A e-Ea/RT and compare it to k = p × Z × e-E/RT
i.e., p × Z = A and E = Ea
Ea is the minimum energy required for a reaction to occur.

Collision theory therefore explains why the rate constant depends on temperature
and defines the rate constant as a product of three factors: Z, f & p. However, it does
not explain the role of the activation energy.
132
 Transition State Theory OR Activated Complexes Theory NOTES:
– focuses on the species formed at the top of the potential barrier, e.g., AB‡

Sample Potential-Energy Diagram for an Exothermic Reaction:

I - I must be stretched

H2 + I2
2HI

Consider the elementary reaction: Cl•(g) + CH4(g) → Cl–H(g) + •CH3(g)

Given: Ea = 16 kJ⋅mol–1 & ∆H = +8 kJ⋅mol–1 (Rxn endothermic since ∆Hº positive.)
Potential-Energy Profile:

Question A:
The bimolecular gas-phase reaction, NO(g) + Cl2(g) → NOCl(g) + Cl(g) has ∆Hº
+83.7 kJ/mol and Ea +84.9 kJ mol-1. The value of the activation energy for the
reverse rxn is:
A) –84.9 Ea(reverse) = Ea - ∆H
= 84.9 - 83.7
C) 84.9 = 1.2
D) 168.6
E) none of these
133
Question B: According to the collision theory of bimolecular gas phase reactions, NOTES:
the activation energy in the Arrhenius model is associated with
A) The potential energy of interaction of two molecules.
B) The frequency of collisions. c) proper orientation—>
C) The fraction of the collisions having the proper orientation. exponential eq∆
D) The pressure of the reactants.
Ea = exponential factor!

REACTION MECHANISMS (section 13.7)

Consider 2 reactions:
1. H2(g) + I2(g) → 2HI(g); rate = k[H2][I2]
2. H2(g) + Br2(g) → 2HBr(g); rate = k[H2][Br2]3/2/{[Br2] + k′[HBr]}
How do we account for complicated rate laws?

Kinetics and Mechanisms

To understand the rates of reactions, to explain the temperature dependence of rates and
(ultimately) explain the mechanism of the reaction, we need to consider some theories of
reaction rates. Reaction mechanisms must involve a series of steps, each an
“elementary” process producing the overall reaction. An overall reaction is made up
of one or more elementary reactions. These are reactions that occur in a SINGLE
step i.e., there are no intermediate reactions.

Types of Elementary Reactions:

one
1. Unimolecular Reactions: _______ molecule reacts/decomposes to give products, e.g., “Unimolecular” - one
O3(g) → O2(g) + O(g) molecule
N2O4(g) → 2NO2(g)
two
2. Bimolecular Reactions: _________ molecules react to give products, e.g.,
NO(g) + O3(g) → NO2(g) + O2(g)
2NO2(g) → N2O4(g)
three
3. Termolecular Reactions: ________ molecules react to give products.
These are RARE - WHY??

Elementary Reactions
Once you know a reaction is an elementary reaction, and this must be determined by
experimentation, the rate law follows from the stoichiometry of the reaction. Thus for
an elementary reaction, but ONLY for an elementary reaction, the rate equation can be
written down just by looking at the balanced chemical equation. This means, for
elementary reactions the of the
elementary reaction.

For example, in the case of the elementary rxn:

the , making it i.e.,

134
 We can think of a MECHANISM as being a sequence of elementary reactions that convert NOTES:
the reactants to products. The sum of all the elementary reactions (mechanistic steps) will
give the overall stoichiometric equation. IF you have a postulated mechanism, the
overall rate law derived from it MUST agree with that which is found by
experiment or the postulated mechanism is wrong! [Recall that the Rate Law can NOT
be predicted from the overall stoichiometric equation.]

The term molecularity can only be applied to an elementary reaction. It describes the
number of chemical species participating in the elementary reaction. For elementary
processes, the molecularity is the same as the overall kinetic order. The kinetic order
of a reaction is what is determined experimentally from the rate equation. You can
talk about the order of the reaction, or the order with respect to any reactant.
Example:
It’s not 2NO2
The reaction of NO2 in the laboratory: CO(g) + NO2(g) → NO(g) + CO2(g) THEREFORE its
follows the following rate experimental law: rate = k[NO2]
bimolecular
(i) Is this an elementary reaction? No ; not “rate = k[NO2]^1 ”
(ii) Does it involve a bimolecular reaction between NO2 and CO?
false ; no dependence on CO! (not included in the rate law!
Answer: If we write a rate law based on the above chemical equation (i.e., assume it was an
elementary reaction), we would have:

rate = k[NO2]^2 rate law is zero/ r/t CO!

Question A: For: A + B → C + D has Ea = 40 kJ mol-1 and ∆H = -12 kJ mol-1. Ea(reverse) = 40 - (-12)

The activation energy (kJ mol-1) for the reverse reaction is: = 52
A) -40 B) 28 D) 12 E) none of these

Question B: For the diagram below, which set of labels is correct?

Reactant Transition State Intermediate Product
A) E B,D C A
B) A B None C
C) C D None E
D) A C B,D E

transition
transition

2 steps in rxn mechanism

D is faster ; requires less energy intermediate
reactant product

135
Reaction Mechanisms – detailed path by which reactants are converted to products. NOTES:
We need to know or predict or guess:
• sequence and type of elementary reactions
• reaction intermediates (energy minima)
• possible transition states (energy maxima)
• energy barriers involved
The overall reaction is obtained by the sequence of elementary reaction steps.
Very often it is
found/implied/suggested/proposed that one of the elementary reaction steps is much slower
than the others; in this case the , which brings us to the
idea of a Rate Limiting Step.

Rate Limiting Reactions (section 13.8)

• The reaction mechanism is the dissection of a complicated reaction sequence into
its elementary steps.
• The overall rate of a complex reaction is the rate of the slowest of these
rate-determining
elementary steps, which is called the ____________________________ or the
rate-limiting step. => has highest E(a)
• In a chemical reaction, the reaction rate is determined by the events leading up
to and including the rate-determining step, but not by the (fast) reactions
which occur afterwards.

Example 1: The following mechanism is suggested for the reaction:

CO(g) + NO2(g) → NO(g) + CO2(g) having an exp’tal rate law: rate = k[NO2]2
Possible Mechanism:
1. 2NO2(g) → NO(g) + NO3(g) (k1, slow)
2. NO3(g) + CO(g) → NO2(g) + CO2(g) (k2, fast)

rate of slow step = K1[NO2]^2

The rate equation then includes 2 moles of NO 2 (slow step of the rxn), but does not
include CO (fast step). Since the rate of the reaction does not depend on the
0
concentration of CO, the reaction is said to be _______–order in CO. We can then
conclude: “The proposed mechanism is consistent with the experimental data."
If one adds up all the steps in the mechanism, you will arrive at the overall stoichiometric
equation and can identify any intermediates in the process:
2NO2(g) → NO(g) + intermediate
+ + CO(g) → NO2(g) + CO2(g)
NO2(g) + CO(g) → NO(g) + CO2(g)
Therefore, NO2 and CO are the reactants while NO and CO2 are the products. An
intermediate
________________________ is a species that is formed and then consumed in a
later step. In this reaction the intermediate is NO3(g) .

Catalysts => affects in 1st and reacts, comes in later and takes product
136
General Energy Profile: NOTES:

slightly exothermic rxn

The overall reaction is exothermic, which is indicated by the fact that the products
are lower than the reactants (you can determine this from calculating ∆HRxn).
Slow steps are slower because there is a larger energy barrier involved in the
reaction while fast steps have a lower Ea.

Example 2:
F2(g) + 2NO(g) → 2ONF(g); experimental rate law: rate = k[NO][F2]
Possible Mechanism:
1. NO(g) + F2(g) → ONF(g) + F(g) (slow)
2. F(g) + NO(g) → ONF(g) (fast)
If this mechanism were true, then it would give rise to the following rate equation:

Conclusion: "Proposed mechanism is ________________ with experimental data."

Reactions with a Rapid Equilibrium Step

For the reaction, 2NO(g) + O2(g) → 2NO2(g), we find experimentally that:
–∆[O2]/∆t = rate = k[NO]2[O2], i.e., third order overall
Possible Mechanism:
2NO(g) U N2O2(g) rapid equilibrium, K1
N2O2(g) + O2(g) → 2NO2(g) slow, k2
Pictorially:

∆H is negative ;
exothermic rxn

137
 d[ O2 ] NOTES:
Based on the slow step: − = rate = k2[N2O2][O2]
dt
Note: N2O2 is a reaction intermediate.

So, we need to do some “chemical algebra” to eliminate intermediates from rate equation.
Based on the equilibrium reaction, we can define:
K1 = [N2O2] / [NO]^2 OR [N2O2] = K1[NO]^2
^ replaces intermediate
Using this relationship, we now can substitute for [N2O2] in the rate law:

–∆[O2]/∆t = rate = k2 K1 [NO]^2 [O2]

From experimental data: –∆[O2]/∆t = rate = kobserved[NO]2[O2]

consistent
We can then conclude: "The proposed mechanism is _______________________
with the experimental data."
Note: Ea for the overall reaction is the energy required to go from the reactants to the top of
the energy barrier for the slowest step.

Alternate Mechanism:
NO(g) + O2(g) U OONO(g), rapid equilibrium, K1
NO(g) + OONO(g) → 2NO2(g), slow, k2
rate = k2[NO][OONO]

Substituting for [OONO]:

K1 = [OONO] / [NO][O2]
[OONO] = K1[NO][O2]
Substitute for [OONO] in the rate law:

–∆[O2]/∆t = rate = k2K1[NO]^2 [O2]

rate = k(observed) [NO]^2 [O2]

This mechanism produces the same rate law as what we saw in the previous case. We would
therefore need further evidence to distinguish between the two mechanisms (i.e., which
intermediate is correct?).
REMEMBER: For a good proposed mechanism, the rate limiting step must be consistent
with the rate law. Also, the sum of all the elementary steps must give the correct
stoichiometric equation.
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ALTERNATE SUBSTITION: NOTES:
Instead of using the equilibrium constant, one can also determine a substitution
expression based on the fact that the forward and reverse rates are equal when a reaction
is at equilibrium. For example, in the case of mechanism #1 above, i.e.,
2NO(g) U N2O2(g) rapid equilibrium, K1
N2O2(g) + O2(g) → 2NO2(g) slow, k2 rate = k2[N2O2] [O2]
The rapid equilibrium step involved: 2NO U N2O2
Based on the definition of equilibrium: rateforward = ratereverse

k1[NO]^2 = k-1[N2O2]
[N2O2] = (k1)/k-1 [NO]^2

where &

Using this relationship to substitute for [N2O2] in the rate law:

rate = k2(k1/k-1) [NO]^2 [O2] , or

rate = NO]2[O2] where

Note: from previous method.

1st order each

Consider the following: H2(g) + I2(g) → 2HI(g); rateobserved = k[H2][I2]
(a) What was taught in high school ~50 year ago: 2nd order overall
H2(g) + I2(g) → 2HI(g) – a bimolecular elementary reaction
(b) Current thinking:
rxn 1: I2 U 2I (fast equilibrium, K1) (2I) - Radicals are
highly reactive!
rxn 2: I + H2 U H2I (fast equilibrium, K2)
rxn 3: H2I + I → 2HI (slow, k3) —> bimolecular process
WHY is this a "better" mechanism?
improved efficiency, able to better understand steps
nd
Using the 2 mechanism, we get: rate = k3[I][H2I]
{both intermediates – need to find substitutions}
Based on rxn#2: K2 = [H2I] / [I][H2] = [H2I] = K2[I][H2]

OR
k2
K2[I][H2] = K-2[H2I] = [H2I] = [I][H2]
k –2

k 2k 3
which gives: rate = K2 k3 [I]2[H2 ] = [I]2[H2 ]
k –2
139
Based on rxn#1: K1 = [I]^2 / [I2] [I]2 = K1[I2] = k1 [I2] NOTES:
k –1

k1 k2 k3
which gives: rate = K1K2 k3 [I2][H2 ] = [I2][H2 ]
k –1 k –2

where rateobserved = kobserved [I2 ] [H2 ]

Chain Reactions
Chain reactions have highly reactive intermediates that react to produce another,
which produces another, which … etc.
e.g., H2 and O2
CH4 and O2 can be mixed with no effect
H2 and Cl2
However, if a reaction is initiated, it goes very rapidly
with a large negative ∆H; i.e., explosion!

For example, in the case of H2 and O2:

Initiating step – creates highly reactive species (e.g., free radicals)
e.g., H2 spark
→ 2H• rate limiting, high E a
slow rate
Branching step – increases number of reactive species; rapid acceleration of rxn.
e.g., H• + O2 → O• + •O•
•O• + H2 → HO• + H•
Propagating step – maintains number of reactive species.
e.g., HO• + H2 → H2O + H•
Terminating step – reduces number of reactive species.
e.g., HO• + H• → H2O
H• + H• → H2

Question A: The following is a proposed mechanism for an overall reaction.

ClO– (aq) + H2O(l) U HOCl(aq) + OH–(aq)
overall:
I–(aq) + HOCl(aq) → HOI(aq) + Cl–(aq)
ClO-(aq) + I-(aq) —> Cl-(aq) + OI-(aq)
HOI(aq) + OH–(aq) → OI–(aq) + H2O(l)
Identify the following species as reactant, catalyst, intermediate or product.
(1) H2O(l) catalyst ; first step ; its a reactant, then is consumed, and shows up in final rxn step
(2) OH–(aq)
i t di t f d d ti 1 t t d 3 d t it i t t di d
(3) I–(aq) reactant ; look @ overall rxn!

140
 Question B: For the following mechanism: NOTES:
overall: 2NO(g) U N2O2(g) K1, fast
2NO(g) —> O2(g) + 2NO2(g) N2O2(g) + O2(g) → 2NO2(g) k2, slow higher Ea!
The rate equation was determined to be: rate = k2 K1 [NO]2 [O2]. For a plot of potential
energy versus progress of reaction, the profile shows
higher Ea!
B. 2 minima representing the 2 reactions.
C. 2 maxima, the 1 st maxima being highest.
D. 1 maximum for the 2nd step.
E. 1 maximum for the 1st step.

Catalysis
Previously we have seen that we can speed up a reaction by , or
. There are two other ways that this can be achieved:
reduce Ea
1. lower the barrier, i.e., _______________
2. improve collision efficiency by i (s).

A increases the reaction rate without itself being used up in the process by
1)
2) assisting in the ,
3) providing the steric for conversion of reactants to products.

There are two kinds of catalysts: homogeneous and heterogeneous

Homogeneous Catalysis: reactants and catalyst are in the same phase.
e.g., the conversion of 2O3(g) → 3O2(g) is catalysed by freons;
molecules like CF2Cl2 which are used in air-conditioners, etc.

Heterogeneous Catalysis: reactants and catalyst are in phases.

e.g., catalytic hydrogenation of alkenes.

Ozone Decomposition:
Uncatalysed mechanism:
O3(g) U O2(g) + O(g) rapid equilibrium, K1
O3(g) + O(g) → 2O2(g) slow, k2
Overall reaction: 2O3(g) → 3O2(g)

½ ∆[O2]/∆t = rate = k2[O3] [O]

K1 =
[O 2 ][O ]
, where [O] = K1[O3] / [O2] Oxygen is an intermediate OR
[O 3 ]
k1[O3] = k–1[O2][O], where [O] = (k1 / k-1) [O3] [O2]

[ O3 ]2
k1k 2 [ O3 ]
2
[ O 3] 2
∴rate = K1 k2 = (where rate = kobs is observed by experiment)
[ O2 ] k–1 [O2 ] [ O2 ]
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Homogenous catalysed mechanism for the slow step in the previous mechanism: NOTES:
CF2Cl2 → Cl• + •CF2Cl
Cl• + O3 → •ClO + O2
•ClO + O → •Cl + O2
Cl• + •CF2Cl → CF2Cl2
Net effect is O3 + O → 2O2, but now no longer "slow".
The catalyst CF2Cl2 emerges unchanged.

Compare Reaction Profiles:

Reference J. Olmsted & G.M. Williams, Chemistry, 3rd ed., John

Wiley & Sons, Inc., New York, 2002, p. 689.

With the catalyst, the overall reaction has lower activation energy than the uncatalysed
reaction. Therefore a larger fraction of molecules will have sufficient energy to exceed E a
and hence participate in the reaction.
To distinguish between a catalyst and an intermediate: A catalyst is present at the beginning and
reacts to form something else. Later the catalyst is reformed unchanged, so it is cancelled out of the
overall reaction. An intermediate must be formed, and then is consumed in a following step.

Heterogeneous Catalysis:
These catalysts are very important to the chemical industry, e.g.,
Fe
Haber process: 3H2(g) + N2(g) → 2NH3(g) (400ºC and 200 atm)
Cu −ZnO/Al O
2 3
2H2(g) + CO(g) → → CH3OH(g)
A catalytic converter in the exhaust system of automobiles provides a catalytic
surface so that the following reactions occur at higher efficiency:
Pt
2CO(g) + O2(g)  → 2CO2(g)
Pt
2NO(g) → N2(g) + O2(g)
¾ Mechanisms involving catalysts are often complex and are not fully understood.
¾ There is a great deal of interest in metal clusters, organometallic chemistry and
surface/surface reactivity for industrial applications.

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You have already seen an example of heterogeneous catalysis from CHEM*1040. During NOTES:
hydrogenation of alkenes, hydrogen is adsorbed to the surface of a metal catalyst (Ni, Pt or
Pd). The surface of the catalyst allows for the weakening of the H–H bond, and thus the
addition of H´s to the alkene.
e.g., H2C=CH2(g) + H2(g) → H3C-CH3(g)
(in the presence of a metal catalyst)
Possible mechanism:
H2C=CH2(surface) + H(surface) → H2C—CH3(surface)
H2C—CH3(surface) + H(surface) → H3C=CH3(g)

¾ Catalysts are also involved in biological processes, such as enzyme catalysis to

allow biochemical process to take place that would otherwise be too slow.
and have active sites where reactions take place allowing for a
better orientation or weaken bonds in reactants, which lowers the Ea.

¾ In this case, another species may react with the catalyst

to inhibit the intended reaction.
e.g., Lead (in gasoline) will poison a catalytic converter in a car
Arsenic(V) when ingested is reduced to As(III) which then binds to the
–SH groups of enzymes inhibit their action.

Problem 1: One pathway for destruction of ozone in the upper atmosphere is:
O3 → O2 + O (rapid equilibrium)
O3 + NO → NO2 + O2 (slow)
NO2 + O → NO + O2 (fast)
2O3 → 3O2 (overall reaction)
The catalyst in this reaction is: (a) O (b) NO2 (c) O3 (d) O2 (e) NO

Problem 2: The rate law for the reaction between chlorine and chloroform, CHCl3
(i.e., CHCl3 + Cl2 → HCl + CCl4) was found to be, rate = kobs[CHCl3][Cl2]½
Show that the following mechanism is consistent with this rate law:
Cl2 → 2 Cl (fast)
CHCl3 + Cl → CCl3 + HCl (slow)
CCl3 + Cl → CCl4 (fast)

Problem 3: Plot energy profiles, and identify Ea(forward), for the following:
i. a slow step followed by a fast step (endothermic).
ii. a fast step followed by a slow step (exothermic rxn).
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Answer 1:
A catalyst is used up and then reformed unchanged. Therefore, NO is the catalyst.
(Others: O – intermediate; NO2 – intermediate; O3 – reactant; O2 – product)

Answer 2:
Rate is determined by the slow step: rate = k2[CHCl3][Cl]
Cl is an intermediate and must be replaced. Use equation one, an equilibrium
reaction, to find a relationship between this intermediate and the reactant(s).
K1 = [Cl]2/ [Cl2]; ∴ [Cl] = {K1[Cl2]}½
Substituting into the rate expression:

rate = k2[CHCl3] {K1[Cl2]}½

rate = k2 K1½[CHCl3] [Cl2]½
rate = k [CHCl3][Cl2]½
This rate expression is the same as the observe rate law, so the proposed mechanism
is consistent with experimental data.

Answer 3:
i. a slow step followed by a fast step (endothermic)

ii. a fast step followed by a slow step (exothermic rxn).

Note, E a for the reaction is the energy required to go from reactants to the top of the
energy barrier for the slow step.

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KINETICS REVIEW QUESTIONS
I. For the diagram provided, identify the one correct answer:
A) The forward reaction is exothermic
B) The forward reaction is endothermic
C) Ea(forward) < Ea(reverse)
D) Ea(forward) = 0
E) Ea(reverse) = 0

II. For the diagram below, which one of the following is true?
Α) ∆H(forward) = C – B
Β) ∆H(forward) = B – A
C) Ea(forward) > Ea(reverse)
D) Ea(reverse) = C – A
E) The potential energy of the transition state is
greater for the forward reaction than for the
reverse reaction.
III. For a simple two-step mechanism: reactants → intermediates → products,
the potential energy diagram shown is obtained. Which
one of the following statements applies?
A) The reactants quickly form intermediates that
slowly form products.
B) The presence of intermediates is difficult to
determine kinetically, although the two-step
reaction is not ultrafast.
C) The intermediates are the final products.
D) The intermediates accumulate in measurable
quantities, and the reaction is easily resolved into
two steps.
E) None of the above.

IV. To establish first-order kinetics unequivocally by graphical methods, which of the following
graphs does one draw?
A) [A] vs. t B) 1/[A] vs. t C) ln[A] vs. t D) ln[A] vs. 1/t E) none of these.

V. To establish second-order kinetics unequivocally by graphical methods, which of the following

graphs does one draw?
A) [A] vs. t B) 1/[A] vs. t C) ln[A] vs. t D) ln[A] vs. 1/t E) none of these.

VI. For a second-order reaction 2A → B, when the concentration of [A] is doubled the value of the
rate changes by a factor of:
A) 0.25 B) 0.5 C) 2 D) 4 E) none of these.

145
VII. The reaction 2NO(g) + O2(g) → 2NO2(g) has the rate equation: rate = k[NO]2[O2]
When an experiment is started with equal concentrations of both reactants,
(i) the rate after 25.0% of the NO has been consumed will be what fraction of the initial rate:
A) 0 B) 0.125 C) 0.188 D) 0.413 E) 0.500 F) none of these.
(ii) the rate after 25.0% of the O2 has been consumed will be what fraction of the initial rate?
A) 0.0625 B) 0.125 C) 0.188 D) 0.413 E) none of these

VIII. The reaction: 2NO(g) + O2(g) → 2NO2(g) is 2nd order in NO and 1 st order in O2. Starting with
equal concentrations of NO and O2, the rate after 50% of the NO has been consumed will be what
fraction of the initial rate?
A) 0.125 B) 2. 0 C) 0.188 D) 0.250 E) 0.413 F) None of these

IX. To establish first-order kinetics unequivocally by graphical methods, one can draw a plot of
ln[A] vs. t (where [A] is the reactant concentration at time t). The slope is then equal to
A) +k B) – k C) ln(2/k) D) 1/k E) none of these.

X. To establish simple second-order kinetics unequivocally by graphical methods, one would plot a
graph of 1/[A]t vs. t. The slope of this graph is then equal to
A) +k B) – k C) 1/( –k) D) 1/k E) none of these.

XI. The reaction A → B is simple second-order in A with a rate constant of 2.0×10-2 L mol-1 s-1 at
25ºC. The time (s) required for 75% reaction of A under these conditions is
A) 0.33 B) 3.0 C) 29 D) 14 E) not enough data given

XII. To determine Ea one measures rate constants (k) at various temperatures (T K) and
i) plots which graph?
A) k vs. T B) 1/k vs. T C) lnk vs. T D) lnk vs. 1/T E) none of these
ii) The slope of the graph is equal to:
A) –Ea B) Ea C) –Ea/R D) Ea/R E) none of these

XIII. The bimolecular gas-phase reaction, NO(g) + Cl2(g) → NOCl(g) + Cl(g) has ∆Hº +83.7 kJ/mol
and Ea +84.9 kJ mol-1. The value of the activation energy for the reverse rxn is:
A) –84.9 B) 1.2 C) 84.9 D) 168.6 E) none of these

XIV. The rxn A → B is 1 st order in A and 1st order overall, with a rate constant = 4.00×10–4 s–1 at
323 K. The percentage of A which will react in a 1.00 hour period is:
A) 0.42 B) 14.4 C) 23.7 D) 69.4 E) 76.3

ANSWERS:
Question Answer(s) Question Answer(s) Question Answer(s)
I. B) VI. D) XI. E)
II. B) VII. E); C) XII. D); C)
III. A) VIII. C) XIII. B)

IV
V. C)
B) IX
X. B)
A) XIV E)

146