The following data were obtained during the first order thermal decomposition of N2O5(g) at a constant volume:
2 N2O5(g)
2 N2O4 + O2(G)

Calculate the rate constant.
OR
Two reactions of the same order have equal pre exponential factors but their activation energies differ by 24. 9 kJ mol - 1. Calculate the ratio between the rate constants of these reactions at 27°C. (Gas constant R = 8. 314 JK - 1mol - 1. )
2 N2O5(g)
2 N2O4 + O2(G)
GIVEN,
At t = 0 0. 5 atm 0 atm 0 atm
At time t 0. 5 - 2x atm 2x atm x atm
To find total pressure:
Pt = sum of partial pressures of all reactants and products
Pt = 0. 5 - 2x + 2x + x
x = pt - 0. 5
p
= 0. 5 - 2x
= 0. 5 - 2(pt - 0. 5)
= 1. 5 - 2pt
At t = 100 s ;pt = 0. 512 atm
p
= 1. 5 - 2
0. 512 = 0. 476 atm
Formula to find rate constant of a first order reaction
k =
log ![]()
k =
log ![]()
k =
0. 0216 = 4. 98
10 - 4 s – 1
conclusion
the rate constant for the following reaction is 4. 98
10 - 4 s - 1
OR
Given:
Difference between activation energies = 24. 9 kJ/mol
The Arrhenius equation: ![]()
take log on both sides, log k = log (Ae-Ea)
log k = log A - ![]()
LETS ASSUME,
For reaction 1 log k1 = log A - ![]()
For reaction 2 log k2 = log A - ![]()
Subtract 1 from 2
![]()
![]()
![]()

Conclusion:
Ratio between rate constants = 2. 198
4
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