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Chemical Kinetics. Chapter 14. Kinetics. Studies the rate at which a chemical process occurs. Besides information about the speed at which reactions occur, kinetics also sheds light on the reaction mechanism (exactly how the reaction occurs). Four main factors affect reaction rates:
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Chemical Kinetics Chapter 14
Kinetics • Studies the rate at which a chemical process occurs. • Besides information about the speed at which reactions occur, kinetics also sheds light on the reaction mechanism (exactly how the reaction occurs). • Four main factors affect reaction rates: • Physical states of reactants • Concentrations of reactants • Temperature • Catalysts
Factors That Affect Reaction Rates • Physical State of the Reactants • In order to react, molecules must come in contact with each other. • The more homogeneous the mixture of reactants, the faster the molecules can react.
Factors That Affect Reaction Rates • Concentration of Reactants • As the concentration of reactants increases, so does the likelihood that reactant molecules will collide.
Factors That Affect Reaction Rates • Temperature • At higher temperatures, reactant molecules have more kinetic energy, move faster, and collide more often and with greater energy.
Factors That Affect Reaction Rates • Presence of a Catalyst • Catalysts speed up reactions by changing the mechanism of the reaction. • Catalysts are not consumed during the course of the reaction.
A B rate = D[A] D[B] rate = - Dt Dt Chemical Kinetics Thermodynamics – does a reaction take place? Kinetics – how fast does a reaction proceed? Reaction rate is the change in the concentration of a reactant or a product with time (M/s). D[A] = change in concentration of A over time period Dt D[B] = change in concentration of B over time period Dt Because [A] decreases with time, D[A] is negative. 14.1
AB rate = D[A] D[B] rate = - Dt Dt 14.1
Br2(aq) + HCOOH (aq) 2Br-(aq) + 2H+(aq) + CO2(g) time Br2(aq) 393 nm 393 nm Detector light D[Br2] aDAbsorption 14.1
Br2(aq) + HCOOH (aq) 2Br-(aq) + 2H+(aq) + CO2(g) slope of tangent slope of tangent slope of tangent [Br2]final – [Br2]initial D[Br2] average rate = - = - Dt tfinal - tinitial instantaneous rate = rate for specific instance in time 14.1
rate k = [Br2] rate a [Br2] rate = k [Br2] = rate constant = 3.50 x 10-3 s-1 14.1
2H2O2 (aq) 2H2O (l) + O2 (g) [O2] = P n V 1 1 D[O2] P = RT = [O2]RT RT RT DP rate = = Dt Dt measure DP over time PV = nRT 14.1
2A B aA + bB cC + dD rate = - = = rate = - = - D[D] D[B] D[A] D[B] D[C] D[A] rate = 1 1 1 1 1 Dt Dt Dt Dt Dt Dt c d a 2 b Reaction Rates and Stoichiometry Two moles of A disappear for each mole of B that is formed. 14.1
Write the rate expression for the following reaction: CH4(g) + 2O2(g) CO2(g) + 2H2O (g) D[CO2] = Dt D[CH4] rate = - Dt D[H2O] = Dt D[O2] = - 1 1 Dt 2 2 14.1
aA + bB cC + dD The Rate Law The rate law expresses the relationship of the rate of a reaction to the rate constant and the concentrations of the reactants raised to some powers. Rate = k [A]x[B]y reaction is xth order in A reaction is yth order in B reaction is (x +y)th order overall 14.2
F2(g) + 2ClO2(g) 2FClO2(g) rate = k [F2]x[ClO2]y Double [F2] with [ClO2] constant Rate doubles x = 1 rate = k [F2][ClO2] Quadruple [ClO2] with [F2] constant Rate quadruples y = 1 14.2
F2(g) + 2ClO2(g) 2FClO2(g) 1 Rate Laws • Rate laws are always determined experimentally. • Reaction order is always defined in terms of reactant (not product) concentrations. • The order of a reactant is not related to the stoichiometric coefficient of the reactant in the balanced chemical equation. rate = k [F2][ClO2] 14.2
Determine the rate law and calculate the rate constant for the following reaction from the following data: S2O82-(aq) + 3I-(aq) 2SO42-(aq) + I3-(aq) rate k = 2.2 x 10-4 M/s = [S2O82-][I-] (0.08 M)(0.034 M) rate = k [S2O82-]x[I-]y y = 1 x = 1 rate = k [S2O82-][I-] Double [I-], rate doubles (experiment 1 & 2) Double [S2O82-], rate doubles (experiment 2 & 3) = 0.08/M•s 14.2
A product rate = [A] M/s D[A] - M = k [A] Dt [A] = [A]0exp(-kt) ln[A] = ln[A]0 - kt D[A] rate = - Dt First-Order Reactions rate = k [A] = 1/s or s-1 k = [A] is the concentration of A at any time t [A]0 is the concentration of A at time t=0 14.3
Decomposition of N2O5 (400 s, -0.34) y = m x + b (2430 s, -1.50) 14.3
The reaction 2A B is first order in A with a rate constant of 2.8 x 10-2 s-1 at 800C. How long will it take for A to decrease from 0.88 M to 0.14 M ? 0.88 M ln 0.14 M = 2.8 x 10-2 s-1 ln ln[A]0 – ln[A] = k k [A]0 [A] [A]0 = 0.88 M ln[A] = ln[A]0 - kt [A] = 0.14 M kt = ln[A]0 – ln[A] = 66 s t = 14.3