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CHAPTER 19 Chemical Kinetics

CHAPTER 19 Chemical Kinetics. Chemical Reactions There are two things that we are interested in concerning chemical reactions: 1) Where is the system going ( chemical equilibrium ). 2) How long will it take for the system to get to where it is going ( chemical kinetics ).

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CHAPTER 19 Chemical Kinetics

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  1. CHAPTER 19 Chemical Kinetics

  2. Chemical Reactions There are two things that we are interested in concerning chemical reactions: 1) Where is the system going (chemical equilibrium). 2) How long will it take for the system to get to where it is going (chemical kinetics). Kinetics is the study of the rate at which a chemical reaction takes place, and the mechanism by which reactants are converted into products.

  3. Example Consider the following irreversible chemical reaction: A(g)  B(g)

  4. Example (continued) We may follow the rate of the reaction by either observing the disappearance of reactant A or the appearance of product B. The average rate of the reaction over some time period from t1 to t2 is: Ave. rate = - ( [A]2 - [A]1) = - [A] t2 - t1 t = ( [B]2 - [B]1 ) = [B] t2 - t1  t where [A] = [A]2 - [A]1 [B] = [B]2 - [B]1 t = t2 - t1 We insert a negative sign when find the rate of disappearance of a reactant to make the rate of reaction positive.

  5. Example (continued) Average rate between 10 s and 20 s is (looking at disappearance of A) Ave. rate = - (0.022 M - 0.030 M) = 0.00080 mol/L.s (20. s - 10. s)

  6. Instantaneous Rate of Reaction The instantaneous rate of reaction at time t is equal to the value for the slope of the tangent line in a plot of concentration vs time (negative if a reactant, positive if a product).

  7. Stoichiometry and Reaction Rate Different reactants (and products) may disappear (or appear) at different rates depending on the stoichiometry of the reaction. For example: H2(g) + 2 ICl(g)  2 HCl(g) + I2(g) In the above reaction ICl disappears twice as fast as H2, and HCl appears twice as fast as I2. To take this into account we can define the average rate of reaction as the change in concentration of a reactant or product divided by the stoichiometric coefficient used to balance the reaction. Ave. rate = - [H2] = - 1[ICl] = 1[HCl] = [I2] t 2 t 2 t t Note we still insert a negative sign when looking at the disappearance of a reactant. By this method we will obtain the same value for average rate no matter which reactant or product we observe.

  8. Rate Law A rate law is an expression that gives the rate of a chemical reaction in terms of the concentrations of the reactants (and occasionally other concentrations as well). For example, consider the following general chemical reaction a A + b B  “products” where a and b are stoichiometric coefficients, and we have assumed the reaction is irreversible (proceeds only in the forward direction). The rate law for reactions of this type can often be written as rate = k [A]m [B]n m = order of reaction with respect to A n = order of reaction with respect to B m + n = overall reaction order k = rate constant, value depends only on temperature. Units determined by dimensional analysis.

  9. For example, for the reaction 2 NO2(g) + F2(g)  2 NO2F(g) rate = - [F2] = k [NO2] [F2] t Reaction is 1st order in NO2, 1st order in F2, and 2nd order overall. Note the following: 1) The reaction orders are usually small whole numbers (0, 1, or 2; occasionally 1/2 or -1; rarely any other values). 2) There is no general relationship between the reaction orders and the stoichiometric coefficients for the reaction. For example, in the above reaction the stoichiometric coefficients for NO2 and F2 are 2 and 1, but the reaction orders (determined by experiment) are 1 and 1.

  10. Experimental Determination of the Rate Law There are several methods that have been developed for finding the rate law for a chemical reaction. The easiest and most common method used is the initial rates method. Consider a general reaction of the form a A + b B  “products” where we assume the rate law for the reaction has the form rate = k [A]m [B]n For a particular set of initial concentrations, the initial rate of reaction is the rate of the reaction measured before the initial concentrations of reactants have had a chance to change significantly. When we measure the initial rate of reaction, we can then use the initial concentrations of our reactants in the rate law.

  11. Consider the following two experiments carried out at the same temperature. trial 1, initial concentrations of A and B are [A]1 and [B]1, initial rate of reaction is R1. trial 2, initial concentrations of A and B are [A]2 and [B]2, initial rate of reaction is R2. R1 = k [A]1m [B]1n R2 = k [A]2m [B]2n Then R2 = k [A]2m [B]2n = ( [A]2/[A]1 )m ( [B]2/[B]1 )n R1 k [A]1m [B]1n The above is true in general. Now, consider the case where the initial concentration of B is the same in both trials.

  12. If [B]2 = [B]1, then ( [B]2/[B]1 )n = 1n = 1 and R2 = ( [A]2/[A]1 )m R1 Since the value expected for m is a small whole number (0, 1, or 2) we can find m from the above equation from inspection. Alternatively, we can take the logarithm of both sides of the equation and solve for m, to get m = ln(R2/R1) ln([A]2/[A]1) The value for n (order of reaction with respect to B) can be found by comparing trials where the initial concentration of A is the same in both trials.

  13. Example The following data were obtained for the reaction A + B  “products” trial initial A initial B initial rate (mol/L) (mol/L) (mol/L.s) 1 0.100 0.100 3.1 x 10-5 2 0.100 0.200 3.0 x 10-5 3 0.200 0.200 1.2 x 10-4 We may assume the rate of reaction is given by the expression rate = k [A]m [B]n Based on the above data, find m, n, and k.

  14. Finding m. Compare trial 3 and trial 2. R3 = k [A]3m [B]3n = ( [A]3/[A]2 )m ([B]3/[B]2 )n R2 k [A]2m [B]2n 1.2 x 10-4 = (0.200/0.100)m (0.200/0.200)n 3.0 x 10-5 4.0 = 2m , and so m = 2 Finding n. Compare trial 2 and trial 1. R2 = k [A]2m [B]2n = ( [A]2/[A]1 )m ([B]2/[B]1 )n R1 k [A]1m [B]1n 3.0 x 10-5 = (0.100/0.100)m (0.200/0.100)n 3.1 x 10-5 0.97 = 2n , and so n = 0 So the rate law is: R = k [A]2

  15. To find k we can now use any of the trials. If we use trial 1, then R1 = k [A]12 k = R1/[A]12 = (3.1 x 10-5 mol/L.s) = 3.1 x 10-3 L/mol.s (0.100 mol/L)2 Notice that the units for k are determined by dimensional analysis. For a real set of experimental data we would find a value for k from each data set, and then average to find the best value for k. Also note for real data the values for the reaction orders would likely not work out to be exactly integers due to experimental error.

  16. For example: Experimental value Reaction order 1.94 = 2n n = 1 9.4 = 3m m = 2 1.45 = 2p p = 1/2 We have assumed in the above that the true values for the reaction orders should be integer or half-integer values, and that the small differences we observe are due to random error in the experimental data.

  17. Typical Types of Rate Laws As previously discussed, the rate law for a reaction can often be written as rate = - [A] = k [A]m [B]n t Common rate laws. Zero order rate = k First order homogeneous rate = k [A] Second order homogeneous rate = k [A]2 Second order heterogeneous rate = k [A] [B]

  18. First Order Homogeneous Rate Law For a first order homogeneous rate law rate = k [A] We may show that concentration vs time is given by the expression [A]t = [A]0 e-kt where [A]t = concentration of A at time t [A]0 = concentration of A at t = 0 k = rate constant (units of 1/time) A plot of concentration vs time will exhibit what is called an exponential decay in the concentration of A.

  19. Finding the Rate Constant It is difficult to find the value for k (rate constant) from a plot of concentration vs time since we get nonlinear behavior. We can find a linear relationship as follows [A]t = [A]0 e-kt Take the ln of both sides ln [A]t = ln [A]0 - kt (y) = b + m(x) y = ln[A]t x = t This predicts that for a first order reaction a plot of ln [A]t vs time will give a straight line, with slope = -k (and intercept = ln [A]0)

  20. One way to test whether or not a reaction is first order is to plot the logarithm of concentration vs time. If you get a linear result in the plot, then you know the reaction is first order. If you do not get a linear result in the plot, then you know the reaction is not first order.

  21. Half-life By definition, the half-life for a chemical reaction, t1/2, is the time it takes for the concentration of a reactant to decrease to 1/2 of its initial value. For a first order reaction [A]t = [A]0 e-kt At t = t1/2, [A]t = [A]0/2, so [A]0/2 = [A]0 e-kt½ Divide both sides by [A]0 then 1/2 = e-kt½ Take the ln of both sides then ln(1/2) = -kt1/2 Divide by -k then t1/2 = - ln(1/2) k But - ln(1/2) = ln(2), so t1/2 = ln(2)0.693 k k

  22. Note the following: 1) Since t1/2 = ln(2)/k for a first order reaction, the value for the half-life is independent of the initial concentration of the reactant. 2) First order reactions are the only reactions where the half-life is independent of concentration. 3) If we wait two half-lives, the concentration will decrease to 1/4 of the initial value. For three half-lives the concentration will decrease to 1/8 of the initial value, and so forth.

  23. Second Order Homogeneous Rate Law For a second order homogeneous rate law rate = k [A]2 we may show that concentration vs time is given by the expression [A]t = [A]0 (1 + kt[A]0) where [A]t = concentration of A at time t [A]0 = concentration of A at t = 0 k = rate constant (units of 1/(concentration)(time)) Concentration will not decrease as quickly in a second order reaction as it does for a first order reaction.

  24. Finding the Rate Constant Since [A]t = [A]0 (1 + kt[A]0) then if we invert both sides of this equation we get 1 = (1 + kt[A]0) = 1 + kt [A]t [A]0 [A]0 (y) = b + m(x) y = 1/[A]t x = t This predicts that for a second order reaction a plot of 1/[A]t vs time will give a straight line, with slope = k (and intercept = 1/[A]0).

  25. One way to test whether or not a reaction is second order is to plot 1/concentration vs time. If you get a linear result in the plot, then you know the reaction is second order. If you do not get a linear result in the plot, you know the reaction is not second order.

  26. Half-life We may use the definition of half-life to find an expression for t1/2 for a second order reaction. It is easiest to do this starting with the expression 1 = 1 + kt [A]t [A]0 If we substitute [A]t = [A]0/2 at t = t1/2, we get (after some algebra) t1/2 = 1 k [A]0 Unlike a first order reaction, the half-life for a second order reaction depends on concentration. As the initial concentration decreases the half life becomes longer.

  27. Zero Order Rate Law For a zero order rate law rate = k [A]0 = k we may show that concentration vs time is given by the expression [A]t = [A]0 - kt , t < [A]0/k = 0 , t  [A]0/k where [A]t = concentration of A at time t [A]0 = concentration of A at t = 0 k = rate constant (units of concentration/time) Concentration decreases at a constant rate until all of the reactant has disappeared.

  28. Finding the Rate Constant and Half-Life Since [A]t = [A]0 - kt , t < [A]0/k a plot of concentration vs time will be a straight line, with slope = -k, (and intercept = [A]0). The half life for a zero order reaction will be t1/2 = [A]0/2k

  29. Summary of Results First order [A]t = [A]0 e-kt Second order [A]t = [A]0 (1 + kt[A]0)

  30. Sample Problem Consider the reaction A  “products” The reaction obeys first order homogeneous kinetics. The initial concentration of A in the system is [A]0 0.418 M. After 100. s the concentration of A is 0.322 M. Find k (the rate constant), and the concentration of A after 500. s.

  31. Consider the reaction A  “products” The reaction obeys first order homogeneous kinetics. The initial concentration of A in the system is [A]0 0.418 M. After 100. s the concentration of A is 0.322 M. Find k (the rate constant), and the concentration of A after 500. s. [A]t = [A]0 e-kt ln([A]t) = ln([A]0) - kt ln([A]t/[A]0) = - kt k = - (1/t) ln([A]t/[A]0) = + (1/t) ln([A]0/[A]t) So k = (1/100. s) ln(.418/.322) = 2.61 x 10-3 s-1. At 500. s, [A]500 = (0.418 M) exp[-(2.61 x 10-3 s-1)(500. s)] = 0.1134 M

  32. Temperature Dependence of the Rate Constant For a reaction that obeys the rate law rate = k [A]m [B]n the rate, and therefore the rate constant, for the reaction usually increases as temperature increases. Experimentally it is found that the temperature dependence of the rate constant for the reaction often follows a simple expression called the Arrhenius equation: k = A e-Ea/RT where k - the rate constant for the reaction A - pre-exponential factor Ea - activation energy for the reaction If we take the ln of both sides of the Arrhenius equation, we get ln(k) = ln(A) - (Ea/R)(1/T)

  33. Example: 2 HI(g)  H2(g) + I2(g) If we assume the data fit the Arrhenius equation, find the values for A and Ea, (including correct units).

  34. Example: 2 HI(g)  H2(g) + I2(g) If we assume the data fit the Arrhenius equation, then ln k = ln A - (Ea/R) (1/T) and so for each experimental value for k and T we must 1) Convert T into units of K, then find 1/T 2) Find the value for ln k and then plot the results.

  35. The value of Ea is found from the slope of the above plot. The value for A is then found by substituting one of the data points into the Arrhenius equation.

  36. x y 0.0013 K-1 - 4.0 0.0018 K-1 - 15.0 At T = 556. K we have k = 3.52 x 10-7 L/mol.s

  37. x y 0.0013 K-1 - 4.0 0.0018 K-1 - 15.0 slope = y = [ (- 15.0) - (-4.0) ] = - 22000. K x [0.0018 - 0.0013]K-1 So Ea = - R (slope) = - (8.314 x 10-3 kJ/mol.K) (- 22000. K) = 182.9 kJ/mol

  38. Since k = A e-Ea/RT, then A = k e+Ea/RT At T = 556. K we have k = 3.52 x 10-7 L/mol.s, and so A = (3.52 x 10-7 L/mol.s) e(182900. J/mol)/(8.314 J/mol.K)(556.K) = 5.37 x 1010 L/mol.s

  39. Other Forms of the Arrhenius Equation Beginning with the Arrhenius equation k = A e-Ea/RT we can derive the following equation ln (k2/k1) = - (Ea/R) 11 T2 T1 In this equation k1 is the rate constant at T1 and k2 is the rate constant at T2. By knowing the value for the rate constant at two different temperatures we may use this equation to find Ea, and then use the value of k at either temperature to find A.

  40. Collision Theory The theoretical model on which the Arrhenius equation is based is called collision theory. The theory makes the following assumptions: 1) For a reaction to take place a collision between reactant molecules must occur. 2) The reactants must collide with sufficient kinetic energy to overcome the energy barrier separating reactants and products. 3) The reactants must have a favorable orientation for reaction to occur. For example, consider the reaction AB + C  A + BC Transition state - The species that forms as reactants are converted into products. It has a structure intermediate between that of the reactants and that of the products of the reaction.

  41. How will the energy of the system change as we proceed from reactants to products? We can represent this by an energy diagram. In this diagram Ea, the activation energy, is the height of the barrier separating the reactants (AB + C) and products (A + BC). Erepresents the change in energy in going from reactants to products. This reaction is exothermic (E < 0). A---B---C is the transition state. Note that it is a good approximation to say H  E.

  42. Collision Theory and the Arrhenius Equation How does collision theory relate to the Arrhenius equation? We can use the theory to give a physical interpretation to the constants that appear in the equation. k = A e-Ea/RT = pz e-Ea/RT A depends on the collision frequency (z, the number of collisions between reactant molecules per unit time) multiplied by an orientation factor (p, the fraction of collisions that have the correct orientation of reactant molecules). e-Ea/RT represents the fraction of collisions that have sufficient kinetic energy to pass over the barrier separating reactants from products. Notice that as T becomes larger, this term also becomes larger, which makes sense, as the molecules move faster and have higher kinetic energy at high temperature than they do at low temperature. Note: As previously discussed in CHM 1045, vave = (3RT/M)1/2

  43. Orientation The pre-exponential factor A in the Arrhenius equation depends on two factors - the rate at which collisions take place and the fraction of collisions that have a favorable orientation for a reaction to occur. k = A e-Ea/RT Example: Cl(g) + NOCl(g)  Cl2(g) + NO(g) Favorable orientation Unfavorable orientation

  44. Reaction Mechanism A reaction mechanism is a sequence of elementary reactions that take place on a molecular level and lead from reactants to products. For example, consider the stoichiometric reaction NO2(g) + CO(g)  NO(g) + CO2(g) One possible mechanism for this reaction is step 1 NO2 + NO2 NO3 + NO step 2 NO3 + CO  NO2 + CO2 In this mechanism NO3 is a reaction intermediate, a substance that is neither a reactant nor a product, but which is produced and consumed as reactants are converted into products.

  45. Types of Elementary Reactions There are three common types of elementary reactions that appear in reaction mechanisms. Unimolecular A  “products” rate = k [A] Bimolecular A + A  “products” rate = k [A]2 A + B  “products” rate = k [A] [B] Termolecular A + A + A  “products” rate = k [A]3 A + A + B  “products” rate = k [A]2 [B] A + B + C  “products” rate = k [A] [B] [C] Note that the rate for a particular elementary reaction is a rate constant multiplied by the concentrations of the reactants.

  46. Requirements For a Reaction Mechanism An acceptable reaction mechanism must satisfy two requirements. 1) The individual elementary steps in the mechanism must add up to the overall reaction. 2) The rate law predicted by the mechanism must agree with the experimentally determined rate law. If the above two requirements are not met, then the reaction mechanism is not acceptable. Unfortunately, the reverse is not true. In principle all we can do with a mechanism is show it is consistent with experiment. Also note that the final expression for the rate law should not involve any reaction intermediates.

  47. Finding the Rate Law From the Reaction Mechanism In general, it is difficult to obtain the rate law for a reaction from the reaction mechanism (in fact, for complicated systems one often uses a computer to model the reaction). There are a few simple cases where we can obtain a rate law from a mechanism: 1) One step mechanism. Examples: O(g) + HBr(g)  OH(g) + Br(g) rate = k [O] [HBr] H+(aq) + OH-(aq)  H2O() rate = k [H+] [OH-]

  48. 2) Mechanisms with a single slow step. For a multistep mechanism with one slow step, the overall rate of the reaction will be the rate of the slow step. This makes it possible to obtain a rate law as long as there are no reaction intermediates involved in the slow step. Example: step 1 H2(g) + ICl(g)  HI(g) + HCl(g) slow step 2 HI(g) + ICl(g)  I2(g) + HCl(g) fast overall H2(g) + 2 ICl  I2(g) + 2 HCl(g) (HI is an intermediate) Since the overall rate of reaction is equal to the rate of the slow step, we may say rate = k1 [H2] [ICl] 1st order in H2, 1st order in ICl 2nd order overall

  49. We can often use experimental data to decide whether a particular reaction mechanism is possible or not. Example: Consider the following two mechanisms for the reaction NO2(g) + CO(g)  NO(g) + CO2(g) One step mechanism NO2(g) + CO(g)  NO(g) + CO2(g) predicted rate law: rate = k1 [NO2][CO] Two step mechanism step 1 NO2(g) + NO2(g)  NO3( g)+ NO(g) slow step 2 NO3(g) + CO(g)  NO2(g) + CO2(g) fast predicted rate law: rate = k1 [NO2]2 Experimentally it is found that this reaction is 0th order in CO and 2nd order in NO2. That means the first mechanism is not correct, and that the second mechanism is consistent with the observed rate law.

  50. Fast and Reversible Elementary Reactions In some reaction mechanisms there will be a step that is both fast and which goes in both directions. k1 A + B C + D fast, reversible k-1 Since the reaction is fast in both directions we can assume that equilibrium is rapidly achieved. At that point, the rate of the forward and reverse reactions must be the same, so k1 [A] [B] = k-1 [C] [D] We can solve the above expression for the concentration of one reactant in terms of other reactants and the rate constants. This is often useful in finding the rate law from a mechanism

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