Rate Law: Second-Order Reaction
2A → B
Rate Law:
Rate = k x [A]2
B appears at same rate that 2A's
disappear
Time (s) [A] [B] K 0.05 M/s
0 1.50 0.00
Reaction
Begins:
Initial
Concentration
Of A is 1.50 M
0 5 10 15 20 25 30 35 40
0
0.2
0.4
0.6
0.8
1
1.2
1.4
1.6
Concentration v Time
A rearranging to B
[A]
[B]
time
Concentration(M)
In first second,
0.11 molar
Reduction in [A]
And 0.06 molar
Increase in [B]
Time [A] [B]
0 1.50 0.00
1 1.39 0.06
0 5 10 15 20 25 30 35 40
0
0.2
0.4
0.6
0.8
1
1.2
1.4
1.6
Second Order Reaction
Rate = k [A]²
[A]
[B]
time (s)
[A](M)
In second
second, rate is
Somewhat
Lower because
[A] is lower
Time [A] [B]
0 1.50 0.00
1 1.39 0.06
2 1.29 0.10
0 5 10 15 20 25 30 35 40
0
0.2
0.4
0.6
0.8
1
1.2
1.4
1.6
Second Order Reaction
Rate = k[A]²
time (s)
[A](M)
After 40 seconds it is easy to
see the steep decay and
product curves.
Time [A] [B]
0 1.50 0.00
5 1.07 0.21
10 0.84 0.33
15 0.69 0.41
20 0.58 0.46
25 0.51 0.50
30 0.45 0.53
35 0.40 0.55
40 0.37 0.57
0 5 10 15 20 25 30 35 40
0
0.2
0.4
0.6
0.8
1
1.2
1.4
1.6
Second Order Reaction
Rate = k[A]²
[A]
[B]
time (s)
[A](M)
Over the same time period,
plotting the natural log of the
concentration v time does
NOT give a straight line.
Time ln[A]
0 0.405
5 0.068
10 -0.174
15 -0.371
20 -0.545
25 -0.673
30 -0.799
35 -0.916
40 -0.994
0 5 10 15 20 25 30 35 40 45
-1.2
-1
-0.8
-0.6
-0.4
-0.2
0
0.2
0.4
0.6
f(x) = -0.034x + 0.229
R² = 0.958
Second order reaction
Ln[A] v time
ln[A]
Linear (ln[A])
time (s)
Ln[A]
However, as suggested by
our analysis, the reciprocal
of [A] v. time is a linear
function, with k as the
coefficient.
Tim
e
1/[A]
0 0.667
5 0.935
10 1.190
15 1.449
20 1.724
25 1.961
30 2.222
35 2.500
40 2.703
0 5 10 15 20 25 30 35 40 45
0
0.5
1
1.5
2
2.5
3
f(x) = 0.051x + 0.678
R² = 1.000
Second Order Reaction
Reciprocal of [A] v time
1/[A]
Linear (1/[A])
time (s)
1/[A](M¯¹)
K = 0.05
This is the effect of changing
the rate constant to 0.01 M/s.
The reaction is much
slower.
Lower Rate Constant
0 5 10 15 20 25 30 35 40
0
0.2
0.4
0.6
0.8
1
1.2
1.4
1.6
Second Order Reaction
Rate = k[A]²
[A]
[B]
time (s)
[A](M)
This is the effect of changing
the rate constant to 0.10 M/s.
The reaction is much faster.
Higher Rate Constant
0 5 10 15 20 25 30 35 40
0
0.2
0.4
0.6
0.8
1
1.2
1.4
1.6
Second Order Reaction
Rate = k[A]²
[A]
[B]
time (s)
[A](M)
This is the effect of changing
the rate constant to 0.10 M/s.
The reaction is much faster.
Higher Rate Constant
0 5 10 15 20 25 30 35 40
0
0.2
0.4
0.6
0.8
1
1.2
1.4
1.6
Second Order Reaction
Rate = k[A]²
[A]
[B]
time (s)
[A](M)

Second orderreactiongraph

  • 1.
    Rate Law: Second-OrderReaction 2A → B Rate Law: Rate = k x [A]2 B appears at same rate that 2A's disappear
  • 2.
    Time (s) [A][B] K 0.05 M/s 0 1.50 0.00 Reaction Begins: Initial Concentration Of A is 1.50 M 0 5 10 15 20 25 30 35 40 0 0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 Concentration v Time A rearranging to B [A] [B] time Concentration(M)
  • 3.
    In first second, 0.11molar Reduction in [A] And 0.06 molar Increase in [B] Time [A] [B] 0 1.50 0.00 1 1.39 0.06 0 5 10 15 20 25 30 35 40 0 0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 Second Order Reaction Rate = k [A]² [A] [B] time (s) [A](M)
  • 4.
    In second second, rateis Somewhat Lower because [A] is lower Time [A] [B] 0 1.50 0.00 1 1.39 0.06 2 1.29 0.10 0 5 10 15 20 25 30 35 40 0 0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 Second Order Reaction Rate = k[A]² time (s) [A](M)
  • 5.
    After 40 secondsit is easy to see the steep decay and product curves. Time [A] [B] 0 1.50 0.00 5 1.07 0.21 10 0.84 0.33 15 0.69 0.41 20 0.58 0.46 25 0.51 0.50 30 0.45 0.53 35 0.40 0.55 40 0.37 0.57 0 5 10 15 20 25 30 35 40 0 0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 Second Order Reaction Rate = k[A]² [A] [B] time (s) [A](M)
  • 6.
    Over the sametime period, plotting the natural log of the concentration v time does NOT give a straight line. Time ln[A] 0 0.405 5 0.068 10 -0.174 15 -0.371 20 -0.545 25 -0.673 30 -0.799 35 -0.916 40 -0.994 0 5 10 15 20 25 30 35 40 45 -1.2 -1 -0.8 -0.6 -0.4 -0.2 0 0.2 0.4 0.6 f(x) = -0.034x + 0.229 R² = 0.958 Second order reaction Ln[A] v time ln[A] Linear (ln[A]) time (s) Ln[A]
  • 7.
    However, as suggestedby our analysis, the reciprocal of [A] v. time is a linear function, with k as the coefficient. Tim e 1/[A] 0 0.667 5 0.935 10 1.190 15 1.449 20 1.724 25 1.961 30 2.222 35 2.500 40 2.703 0 5 10 15 20 25 30 35 40 45 0 0.5 1 1.5 2 2.5 3 f(x) = 0.051x + 0.678 R² = 1.000 Second Order Reaction Reciprocal of [A] v time 1/[A] Linear (1/[A]) time (s) 1/[A](M¯¹) K = 0.05
  • 8.
    This is theeffect of changing the rate constant to 0.01 M/s. The reaction is much slower. Lower Rate Constant 0 5 10 15 20 25 30 35 40 0 0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 Second Order Reaction Rate = k[A]² [A] [B] time (s) [A](M)
  • 9.
    This is theeffect of changing the rate constant to 0.10 M/s. The reaction is much faster. Higher Rate Constant 0 5 10 15 20 25 30 35 40 0 0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 Second Order Reaction Rate = k[A]² [A] [B] time (s) [A](M)
  • 10.
    This is theeffect of changing the rate constant to 0.10 M/s. The reaction is much faster. Higher Rate Constant 0 5 10 15 20 25 30 35 40 0 0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 Second Order Reaction Rate = k[A]² [A] [B] time (s) [A](M)