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Reaction Kinetics PDF

This document discusses reaction kinetics and methods for determining reaction rates: 1) Reaction rates can be determined by measuring changes in concentrations of reactants or products over time using methods like colorimetry or measuring gas volumes/pressures. 2) Reaction rates are represented by rate equations that show the dependence of rate on reactant concentrations and rate constants. The order of a reaction indicates the power to which the concentration of a reactant is raised in the rate equation. 3) Reaction mechanisms involve rate-determining steps that are identified by analyzing which species appear in the overall rate equation. Catalysts provide alternative reaction pathways to increase rates.

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0% found this document useful (0 votes)
44 views10 pages

Reaction Kinetics PDF

This document discusses reaction kinetics and methods for determining reaction rates: 1) Reaction rates can be determined by measuring changes in concentrations of reactants or products over time using methods like colorimetry or measuring gas volumes/pressures. 2) Reaction rates are represented by rate equations that show the dependence of rate on reactant concentrations and rate constants. The order of a reaction indicates the power to which the concentration of a reactant is raised in the rate equation. 3) Reaction mechanisms involve rate-determining steps that are identified by analyzing which species appear in the overall rate equation. Catalysts provide alternative reaction pathways to increase rates.

Uploaded by

jesie dewangker
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Chemistry (A-level)

Reaction kinetics (Chapter 22)

 Rate of reaction can be found by measuring the a decrease or an increase in a particular


reactant or product over a period of time; unit: mol dm -3 s-1

 Methods to find rate of reaction:


 Colorimetry can be used to monitor colour changes of a particular reactant, e.g.
iodine with propanone (fading colour of iodine):

 Changes in gas volume or gas pressure, e.g. benzenediazonium chloride and water:

 Table 22.1 shows measurements taken at the same temperature:

 [propene] means ‘concentration of propene’


 Figure 22.5 showing the reaction graphically:
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 Concentration of propene increases from 0.00 to 0.27 mol dm-3 in the first 5
minutes, hence average rate of reaction:

 To calculate the rate at a particular point on the curve:

 Calculate the gradient of the tangent (rate of reaction):

 The value of -6.67 10-4 refers to the rate of change of cyclopropane


concentration
 As time passes, concentration of cyclopropane falls; graph of [cyclopropane] against time:
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 Table shows that the rate is directly proportional to the concentration of


cyclopropane, hence:

 Rate of reaction given by:

 K is the rate constant


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 Finding the rate of reaction through experiments (e.g. equation 3):


 Find the effect of H2 (g) on the rate by varying the concentration of H2 (g), while
keeping the concentration of NO (g) constant
 Results show that the rate is proportional to the concentration of hydrogen (rate =
k1 [H2])
 Find the effect of NO (g) on the rate by varying the concentration of NO (g), while
keeping the concentration of H2 (g) constant
 Results show that the rate is proportional to the square of the concentration of NO
(rate = k2 [NO]2)
 Combining gives: rate = k1 [H2] [NO]2
 The order of reaction with respect to a particular reactant is the power to which the
concentration of that reactant is raised in the rate equation
 E.g. equation 3, first-order with respect to H2, second-order with respect to NO,
third-order overall (as the sum of the powers is 1 + 2 = 3)
 For a reaction that is A + B → products, rate of reaction given by:

 [A] and [B] are the concentrations of the reactants


 m and n are the orders of the reaction
 The values of m and n can be 0, 1, 2, 3 or rarely higher
 When the value of m or n is 0 we can ignore the concentration term because any
number to the power of zero = 1.

Graph of reaction rate against concentration


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Graph of concentration of reactant against time

 For first- and second-order reactions, the graph is a curve – distinguished by


determining successive half-lives of the reaction
 Half-life, t1/2, is the time taken for the concentration of a reactant to fall to half its original
value

 Zero-order reaction has successive half-lives which decrease with time


 First-order reaction has a constant half-life, where half-life is independent to the
concentration
 Second-order reaction has successive half-lives which increase with time
 Calculating k from half-life (first-order reactions):

 t1/2 is the half-life, units: s


 Rate-determining step: the slowest step in a reaction mechanism
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 E.g. to find the rate-determining step:

 Rate = k[CH3COCH3] [H+]


 Where the slow step (rate-determining step) does not involve propanone or
hydrogen ion directly, however the intermediate with the formula:

 Is derived from substances that react together to form it, hence propanone and
hydrogen ion appear in the rate equation
 E.g. propanone and bromine in alkaline solution:

 Rate = k[CH3COCH3] [OH-]


 Catalysis provides alternative pathway for the reaction with lower activation energy, hence
increasing the rate of reaction
 Homogeneous catalysis occurs when the catalyst is in the same phase as the reaction
mixture
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 Often involves changes in oxidation number of the ions involved in catalysis


 The catalytic role of Fe3+ in the I-/S2O82- reaction:

 Fe3+ (aq) catalyses this reaction involving two redox reactions:

 The catalytic role of atmospheric oxides of nitrogen in the oxidation of atmospheric


sulfur dioxide:
 One of the steps in the formation of acid rain is the oxidation of sulfur
dioxide to sulfur trioxide:

 Catalysed by nitrogen(IV) oxide

 Heterogeneous catalysis occurs when the catalyst is in a different phase to the reaction
mixture
 Often involves gaseous molecules reacting at the surface of a solid catalyst
 Can be explained using the theory of adsorption onto the catalyst’s surface
 Adsorb means to bond to the surface
 Absorb means to move right into the substance
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 Iron in the Haber process (Fe catalyst):


 Diffusion, adsorption, reaction and desorption

 The catalytic removal of oxides of nitrogen from the exhaust gases of car engines:
 Adsorption, weakening of covalent bonds, formation of new bonds and
desorption
 Small beads coated with platinum catalysts

 Example questions:
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 Another method of finding the rate of reaction:


 Sampling followed by titration can be used where small amounts of the reaction
mixture are withdrawn by pipette at regular intervals; further reaction in this
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sample is prevented or slowed down, e.g. by cooling the sample in ice; the
concentration of one of the reactants or products is then determined by titration of
the samples; common examples are the formation of an acid and an iodination
reaction

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