Exercise 12.2
The decomposition of N2O5 in the gas phase was studied at constant temperature.
2 N2O5 (g) à 4 NO2 (g) + O2 (g)
The following results were collected:
[N2O5] Time (s)
0.1000 0
0.0707 50
0.0500 100
0.0250 200
0.0125 300
0.00625 400
Determine the rate law and calculate the value of k.
Exercise 12.3
Using the data given in Ex. 12.2 above, calculate [N2O5] at 150 s after the start of the reaction.
Calculate the [N2O5] at the following times:
200 s
400 s
600 s
1,000 s
12.2) Prepare the following table.
|
Time (s) |
[N2O5] (M) |
ln [N2O5] |
1/[N2O5] (M-1) |
|
0 |
0.1000 |
-2.3026 |
10.0000 |
|
50 |
0.0707 |
-2.6493 |
14.1443 |
|
100 |
0.0500 |
-2.9957 |
20.0000 |
|
200 |
0.0250 |
-3.6889 |
40.0000 |
|
300 |
0.0125 |
-4.3820 |
80.0000 |
|
400 |
0.00625 |
-5.0752 |
160.0000 |
Plot [N2O5] vs time, ln [N2O5] vs time and 1/[N2O5] vs time as below.

Plot of [N2O5] vs time

Plot of ln [N2O5] vs time

Plot of 1/[N2O5] vs time
The plot of ln [N2O5] vs time is linear with a slope equal to -0.0069.
The integrated rate law for a first order reaction is of the form
ln [A] = -kt +ln [A]0
The left side is dimensionless while t (time) has unit s; therefore, k must have unit s-1. Comparing the regression equation with the integrated rate law, we can conclude that the first order rate constant is k = 0.0069 s-1 (ans).
Exercise 12.2 The decomposition of N2O5 in the gas phase was studied at constant temperature. &nbs