Chapter 6 Reaction Kinetics Flashcards

1
Q

The rate of reaction refers to the change in the amount or concentration of a reactant or product per unit time and can be found by:

A
  • Measuring the decrease in the concentration of a reactant OR
  • Measuring the increase in the concentration of a product over time
    • The units of rate of reaction are mol dm-3 s-1
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2
Q

Rate equation

A
  • The thermal decomposition of calcium carbonate (CaCO3) will be used as an example to study the rate of reaction

CaCO3 (s) → CaO (s) + CO2 (g)

  • The rate of reaction at different concentrations of CaCO3 is measured and tabulated
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3
Q

Rate of reactions table

A
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4
Q
  • Rate equations can only be determined experimentally and cannot be found from the stoichiometric equation
A

Rate of reaction = k [A]m [B]n

[A] and [B] = concentrations of reactants

m and n = orders of the reaction

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5
Q

Order of reaction

A
  • The order of reaction shows how the concentration of a reactant affects the rate of reaction
    • It is the power to which the concentration of that reactant is raised in the rate equation
    • The order of reaction can be 0, 1,2 or 3
    • When the order of reaction of a reactant is 0, its concentration is ignored
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6
Q

The overall order of reaction is

A
  • the sum of the powers of the reactants in a rate equation
  • For example, in the following rate equation, the reaction is:

Rate = k [NO2]2[H2]

    • Second-order with respect to NO
      • First-order with respect to H2
      • Third-order overall (2 + 1)
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7
Q

Half-life

A
  • The half-life (t1/2) is the time taken for the concentration of a limiting reactant to become half of its initial value
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8
Q

The rate-determining step is the

A
  • slowest step in a reaction
  • If a reactant appears in the rate-determining step, then the concentration of that reactant will also appear in the rate equation
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9
Q

a bimolecular reaction

A
  • Bimolecular: two species involved in the rate-determining step
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10
Q

Unimolecular:

A

one species involved in the rate-determining step

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11
Q

The intermediate is derived from

A

substances that react together to form it in the rate-determining step

  • For example, for the reaction above the intermediate would consist of CH3Br and OH-
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12
Q

The order of reaction shows how the concentration of a

A
  • reactant affects the rate of reaction

Rate = k [A]m [B]n

  • When m or n is zero = the concentration of the reactants does not affect the rate
  • When the order of reaction (m or n) of a reactant is 0, its concentration is ignored
  • The overall order of reaction is the sum of the powers of the reactants in a rate equation
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13
Q

In a zero-order the concentration of the reactant is

A

inversely proportional to time

  • This means that the concentration of the reactant decreases with increasing time
  • The graph is a straight line going down
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14
Q

In a first-order reaction the concentration of the reactant

A
  • decreases with time
    • The graph is a curve going downwards and eventually plateaus
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15
Q

In a second-order reaction the concentration of the reactant

A

decreases more steeply with time

  • The concentration of reactant decreases more with increasing time compared to in a first-order reaction
  • The graph is a steeper curve going downwards
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16
Q

The progress of the reaction can be followed by measuring the

A
  • initial rates of the reaction using various initial concentrations of each reactant
  • These rates can then be plotted against time in a rate-time graph
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17
Q

In a zero-order reaction the rate doesn’t depend on the

A
  • concentration of the reactant
    • The rate of the reaction therefore remains constant throughout the reaction
    • The graph is a horizontal line
    • The rate equation is rate = k
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18
Q

In a first-order reaction the rate is

A

directly proportional to the concentration of a reactant

  • The rate of the reaction decreases as the concentration of the reactant decreases when it gets used up during the reaction
  • The graph is a straight line
  • The rate equation is rate = k [A]
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19
Q

In a second-order reaction, the rate

A
  • is directly proportional to the square of concentration of a reactant
    • The rate of the reaction decreases more as the concentration of the reactant decreases when it gets used up during the reaction
    • The graph is a curved line
    • The rate equation is rate = k [A]2
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20
Q
  • The order of a reaction can also be deduced from its half-life (t1/2 )
  • For a zero-order reaction the successive half-lives decrease
A

with time

  • This means that it would take less time for the concentration of reactant to halve as the reaction progresses
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21
Q

The half-life of a first-order reaction remains constant throughout the reaction

A
  • The amount of time required for the concentration of reactants to halve will be the same during the entire reaction
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22
Q

For a second-order reaction, the half-life increases with time

A
  • This means that as the reaction is taking place, it takes more time for the concentration of reactants to halve
23
Q

Half-lives of zero, first and second-order reactions

A
24
Q

The initial rate can be calculated by using the

A

initial concentrations of the reactants in the rate equation

25
Q

The half-life of a first-order reaction is independent of the

A

concentration of reactants

  • This means that despite the concentrations of the reactants decreasing during the reaction
  • The amount of time taken for the concentrations of the reactants to halve will remain the same throughout the reaction
  • The graph is a straight line going downwards
26
Q

Experimental data of the changes in concentration over time suggests that the half-life is

A
  • constant
    • Even if the half-lives are slightly different from each other, they can still be considered to remain constant
  • This means that no matter what the original concentration of the CH3CN is, the half-life will always be around 10.0 minutes
27
Q

In a first-order reaction, the time taken for the concentration to halve remains constant

A
28
Q

The rate constant (k) of a reaction can be calculated using:

A
  • The initial rates and the rate equation
  • The half-life
29
Q

Calculating the rate constant from the initial rate

A
  • The reaction of calcium carbonate (CaCO3) with chloride (Cl-) ions to form calcium chloride (CaCl2) will be used as an example to calculate the rate constant from the initial rate and initial concentrations
  • The reaction and rate equation are as follows:

CaCO3 (s) + 2Cl- (aq) + 2H+ (aq) → CaCl2 (aq) + CO2 (g) + H2O (l)

Rate = k [CaCO3] [Cl-]

  • The progress of the reaction can be followed by measuring the initial rates of the reaction using various initial concentrations of each reactant
30
Q

Calculating the rate constant from the half-life

A
  • The rate constant (k) can also be calculated from the half-life of a reaction
  • You are only expected to deduce k from the half-life of a first-order reaction as the calculations for second and zero-order reactions are more complicated
31
Q
  • For a first-order reaction, the half-life is related to the rate constant by the following expression:
A
  • Rearranging the equation to find k gives:
  • So, for a first-order reaction such as the methyl (CH3) rearrangement in ethanenitrile (CH3CN) with a half-life of 10.0 minutes the rate constant is:

= 1.16 x 10-3 dm3 mol-1 s-1

32
Q

The reaction mechanism of a reaction describes how many steps are involved in the

A
  • making and breaking of bonds during a chemical reaction
33
Q

It is the slowest step in a reaction and includes the reactants that have an impact on the reaction rate when their concentrations are changed

  • Therefore, ll reactants that therefore appear in the
A
  • rate equation will also appear in the rate-determining step
  • This means that reactants that have a zero-order and intermediates will not be present in the rate-determining step
34
Q

The overall reaction equation and rate equation can be used to

A

predict a possible reaction mechanism of a reaction

35
Q

The order of a reactant and thus the rate equation can be deduced from a

A

reaction mechanism given that the rate-determining step is known

36
Q

Identifying the rate-determining step

A
  • from a rate equation given that the reaction mechanism is known
  • For example, propane (CH3CH2CH3) undergoes bromination under alkaline solutions
  • The overall reaction is:

CH3CH2CH3 + Br2 + OH- → CH3CH2CH2Br + H2O + Br-

  • The reaction mechanism is:
  • The rate equation is:

Rate = k [CH3CH2CH3] [OH-]

  • From the rate equation, it can be deduced that only CH3COCH3 and OH- are involved in the rate-determining step and not bromine (Br2)
  • Since only in step 1 of the reaction mechanism are CH3COCH3 and OH- involved, the rate-determining step is step 1 is the case for step 1 of the reaction mechanism
37
Q

Identifying intermediates & catalyst

A
  • When a rate equation includes a species that is not part of the chemical reaction equation then this species is a catalyst
38
Q

Identifying intermediates & catalyst

A
  • For example, the halogenation of butanone under acidic conditions
  • The reaction mechanism is:
  • The rate equation is:

Rate = k [CH3CH2COCH3] [H+]

  • The H+ is not present in the chemical reaction equation but does appear in the rate equation
    • H+ must therefore be a catalyst
  • Furthermore, the rate equation suggest that CH3CH2COCH3 and H+ must be involved in the rate-determining (slowest) step
  • The CH3CH2COCH3 and H+ appear in the rate-determining step in the form of an intermediate (which is a combination of the two species)
39
Q

At higher temperatures, a greater proportion of molecules have energy greater than than the

A
  • activation energy
  • Since the rate constant and rate of reaction is directly proportional to the fraction of molecules with energy equal or greater than the activation energy, then at higher temperatures:
    • The rate constant increases
    • The rate of reaction increases
40
Q
  • The relationship between the rate constant and the temperature is given by the following equation:
A

ln k = natural logarithm of the rate constant

A = constant related to the collision frequency and orientation of the molecules

Ea = activation energy (joules, J)

R = gas constant (8.31 J K-1 mol-1)

T = temperature (kelvin, K)

41
Q

The graph of ln k over 1/T is a straight line with gradient -Ea/R

A
  • A varies only a little bit with temperature, it can be considered a constant
  • Ea and R are also constants
  • The equation shows that an increase in temperature (higher value of T) gives a greater value of ln k (and therefore a higher value of k)
  • Since the rate of the reaction depends on the rate constant (k) an increase in k also means an increased rate of reaction
42
Q

Catalysts increase the rate of reaction by providing an alternative

A
  • pathway which has a lower activation energy
  • Catalysts can be either homogeneous or heterogeneous
  • Homogeneous catalysts are those that are in the same phase as the reaction mixture
  • For example, in the esterification of ethanoic acid (CH3COOH) wit
43
Q

In heterogeneous catalysis, the molecules react at the

A
  • surface of a solid catalyst
  • The mode of action of a heterogeneous catalyst consists of the following steps:
  • Adsorption (or chemisorption) of the reactants on the catalyst surface
    • The reactants diffuse to the surface of the catalyst
    • The reactant is physically adsorbed onto the surface by weak forces
    • The reactant is chemically adsorbed onto the surface by stronger bonds
    • Chemisorption causes bond weakening between the atoms of the reactants
  • Desorption of the products
    • The bonds between the products and catalyst weaken so much that the products break away from the surface
44
Q

In the Haber process ammonia (NH3) is produced from

A

nitrogen (N2) and hydrogen (H2)

45
Q

An iron catalyst is used which

A
  • speeds up the reaction by bringing the reactants close together on the metal surface
  • This increases their likelihood to react with each other
46
Q

The mode of action of the iron catalyst is as follows:

A
  • Diffusion of the nitrogen and hydrogen gas to the iron surface
  • Adsorption of the reactant molecules onto the iron surface by forming bonds between the iron and reactant atoms
    • These bonds are so strong that they weaken the covalent bonds between the nitrogen atoms in N2 and hydrogen atoms in H2
    • But they are weak enough to break when the catalysis has been completed
  • The reaction takes place between the adsorbed nitrogen and hydrogen atoms which react with each other on the iron surface to form NH3
  • Desorption occurs when the bonds between the NH3 and iron surface are weakened and eventually broken
  • The formed NH3 diffuses away from the iron surface
47
Q

Iron brings the nitrogen and hydrogen closer together so that they can react and hence increases the rate of reaction

A
47
Q

Iron brings the nitrogen and hydrogen closer together so that they can react and hence increases the rate of reaction

A
48
Q

Heterogeneous catalysts are also used in the

A
  • catalytic removal of oxides of nitrogen from the exhaust gases of car engines
  • The catalysts speed up the conversion of:
    • Nitrogen oxides (NOy) into harmless nitrogen gas (N2)
    • Carbon monoxide (CO) into carbon dioxide (CO2)
49
Q

The catalytic converter has a honeycomb structure containing small beads coated with

A

platinum, palladium, or rhodium metals which act as heterogeneous catalysts

50
Q

The mode of action of the catalysts is as following

A
    • Adsorption of the nitrogen oxides and CO onto the catalyst surface
      • The weakening of the covalent bonds within nitrogen oxides and CO
      • Formation of new bonds between:
        • Adjacent nitrogen atoms to form N2 molecules
        • CO and oxygen atoms to form CO2 molecules
      • Desorption of N2 and CO2 molecules which eventually diffuse away from the metal surface
51
Q

Homogeneous catalysis often involves

A
  • redox reactions in which the ions involved in catalysis undergo changes in their oxidation number
    • As ions of transition metals can change oxidation number they are often good catalysts
  • Homogeneous catalysts are used in one step and are reformed in a later step
52
Q

This is a very slow reaction in which the peroxydisulfate (S2,O82- ) ions oxidise the

A
  • iodide to iodine

S2O82- (aq) + 2I- (aq) → 2SO42- (aq) + I2 (aq)

  • Since both the S2O82- and I- ions have a negative charge, it will require a lot of energy for the ions to overcome the repulsive forces and collide with each other
  • Therefore, Fe3+ (aq) ions are used as a homogeneous catalyst
  • The catalysis involves two redox reactions:
    • First, Fe3+ ions are reduced to Fe2+ by I-

2Fe3+ (aq) + 2I- (aq) → 2Fe2+ (aq) + I2 (aq)

  • Then, Fe2+ is oxidized back to Fe3+ by S2O82-

2Fe2+ (aq) + S2O82- (aq) → 2Fe3+ (aq) + 2SO42- (aq)

  • By reacting the reactants with a positively charged Fe ion, there are no repulsive forces, and the activation energy is significantly lowered
  • The order of the two reactions does not matter
    • So, Fe2+ can be first oxidised to Fe3+ followed by the reduction of Fe3+ to Fe2+
53
Q

Nitrogen oxides & acid rain

A
  • As fossil fuels contain sulfur, burning the fuels will release sulfur dioxide which oxidises in air to sulfur trioxide, and then dilute sulfuric acid (H2SO4) is formed by reaction with water. The result is acidification of rain:

SO3(g) + H2O(l) → H2SO4(aq)

  • Nitrogen oxides can act as catalysts in the formation of acid rain by catalysing the oxidation of SO2 to SO3

NO2(g) + SO2(g) → SO3(g) + NO(g)

  • The formed NO gets oxidised to regenerate NO2

NO(g) + ½ O2(g) → NO2(g)

  • The regenerated NO2 molecule can again oxidise another SO2 molecule to SO3 which will react with rainwater to form H2SO4 and so on