Understanding Rate Laws: First and Second Order, Study notes of Law

An explanation of rate laws, focusing on first-order and second-order reactions. It covers the differential and integrated rate laws, the relationship between the initial concentration and time, and how to determine the rate constant. The document also includes examples and exercises to help students understand the concepts.

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Integrated Rate Law
2 types of rate laws
The differential rate law (what we
have already done, often called simply
the rate law) shows how th e rate of
reaction depends on concentration.
The integrated rate law shows how
the concentrations of species in the
reaction depend on time.
Once you have either the differential
rate law or the integrated rate law, you
easily convert to the other.
Whichever type is easiest to find
usually dictates which type of rate law
is determined experimentally.
Rate Law
A first-order reaction (n t he exponent
is 1) means that as the con centration
doubles, the rate also doubles, etc.
Differential Rate law Equation:
Rate = k [A]
1
The integrated rate laws is looking at
how the concentration changes with
time.
Rate = k[A]
Integrated rate law:
ln[A]
t
- ln[A]
o
= –kt
ln is the natural log, it is reversed by raising the
expression to e
[A]
t
= concentration of A at time t
k = rate constant
t = time
[A]
o
= initial concentration of A
First-Order Rate Law
Important things to note from the p revious
equation.
The equation shows how the concentration of
A depends on time.
If the initial concentration of A and the rate
constant k are known, the concentration of A
at any time can be calculated.
Plot of ln[N
2
O
5
] vs. Time First Order Reaction
Thus, for a first-order reaction,
plotting the natural logarithm of
concentration vs. time alwa ys gives a
straight line.
This is used to test whether a
reaction is first order or not.
This integrated rate law for a first-
order reaction also can b e expressed in
terms of a ratio of [A] and [A]
o
as
follows:
ln[A] = -kt +ln[A]
o
kt = ln[A]
o
- ln[A]
kt = ln ([A]
o
/[A])
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Integrated Rate Law

2 types of rate laws The differential rate law (what we have already done, often called simply the rate law) shows how the rate of reaction depends on concentration. The integrated rate law shows how the concentrations of species in the reaction depend on time. Once you have either the differential rate law or the integrated rate law, you easily convert to the other.  Whichever type is easiest to find usually dictates which type of rate law is determined experimentally. Rate Law A first-order reaction (n the exponent is 1) means that as the concentration doubles, the rate also doubles, etc. Differential Rate law Equation: Rate = k [A]^1 The integrated rate laws is looking at how the concentration changes with time.  Rate = k[A]  Integrated rate law: ln[A]t - ln[A]o = –kt ln is the natural log, it is reversed by raising the expression to e [A]t = concentration of A at time t k = rate constant t = time [A]o = initial concentration of A First-Order Rate Law  Important things to note from the previous equation.  The equation shows how the concentration of A depends on time.  If the initial concentration of A and the rate constant k are known, the concentration of A at any time can be calculated. Plot of ln[N 2 O 5 ] vs. Time First Order Reaction Thus, for a first-order reaction, plotting the natural logarithm of concentration vs. time always gives a straight line. This is used to test whether a reaction is first order or not. This integrated rate law for a first- order reaction also can be expressed in terms of a ratio of [A] and [A]o as follows: ln[A] = -kt +ln[A]o  kt = ln[A]o - ln[A]  kt = ln ([A]o/[A])

Decomposition of N 2 O 5 The following data shows the concentration of over N 2 O 5 time  2N 2 O 5 (g)  4NO 2 (g) + O 2 (g) [N2O5] (mol/L) Time (s) 0.1000 0. 0.0707 50. 0.0500 100. 0.0250 200. 0.0125 300. 0.00625 400. [N 2 O 5 ] over time Time (s) [NO^2 ] (M) 5 0

0 50 100 150 200 250 300 350 400 450 Problem Using this data, verify that the rate law is first order in [N 2 O 5 ], and calculate the value of the rate constant. Answer  You verify it is a first order rate law by graphing. If the graph of the ln[A] v t is a straight line then it is first order. slope  The slope of this line is –k.  Slope is rise over run or the change in y value, ln [N 2 O 5 ], over the change in x value, time.  You can choose any 2 points on a straight line since the slope will not change.  I will arbitrarily chose the first and last points  Slope = -5.075- (-2.303) = -.00693s-  400-0s  Slope = -k so k = 0.00693s- First Order Rate Laws Using the data in the previous example, calculate [N 2 O 5 ] at 150 s after the start of the reaction. k = 0.00693s-1^ [N2O5] (mol/L) Time (s) 0.1000 0. 0.0707 50. 0.0500 100. 0.0250 200. 0.0125 300. 0.00625 400. Answer  ln[N 2 O 5 ] = -kt +ln[N 2 O 5 ]o  k = 0.  t = 150 s  [N 2 O 5 ]o = .100 M ln[N 2 O 5 ]o= -2.  ln[N 2 O 5 ] = -(.00693)150+ -2.  ln[N 2 O 5 ] = -3.  [N 2 O 5 ] = e-3.  [N 2 O 5 ] = .035 M Half life of a first order reaction The time required for a reactant to reach half its original concentration is called the half-life of a reactant. Equation k = rate constant Half–life does not depend on the concentration of reactants. t 12 =^ 0.693k Problem A certain first-order reaction has a half-life of 20.0 minutes. a. Calculate the rate constant for this reaction. b. How much time is required for this reaction to be 75% complete?

Plot of [A] vs Time 29  Half–Life: k = rate constant [A]o = initial concentration of A  Half–life gets shorter as the reaction progresses and the concentration of reactants decrease. Zero-Order

1 ^ ^0

2 = A t (^2) k Concept Check How can you tell the difference among 0th, 1st, and 2 nd^ order rate laws from their graphs? For the zero-order reaction, the graph of concentration versus time is a straight line with a negative slope. For a first-order graph, the graph is a natural log function. The second-order graph looks similar to the first-order, but with a greater initial slope. Students should be able to write a conceptual explanation of how the half-life is dependent on concentration (or in the case of first-order reactions, not dependent). Summary of the Rate Laws Equation sheet of the AP test  On the current equations sheet, they give you zero, first and second order integrated rate law, and first order half life equation. Although they are not labeled. Graphs (all v time) [A] ln[A] 1/[A]  Zero order  First order  Second order Exercise Consider the reaction aA  Products. [A] 0 = 5.0 M and k = 1.0 x 10–2^ (assume the units are appropriate for each case). Calculate [A] after 30. seconds have passed, assuming the reaction is: a) Zero order b) First order c) Second order 4.7 M 3.7 M 2.0 M