The correct option is
A 0.002
According to the Arrhenius equation, K=Ae−Ea/RT
Where A is proportionality constant, Ea is activation energy, R is universal gas constant and T is the temperature in kelvin.
Taking log both sides,
We get, logk = logA - Ea/2.303RT
So, for 1st reaction , logk₁ = logA - Ea₁/2.303RT
For 2nd reaction, logk₂ = logA - Ea₂/2.303RT
Subtracting equation (2) from equation (1),
logk₁ - logk₂ = (Ea₁ - Ea₂)/2.303RT
Here, (Ea₁ - Ea₂) = 41.9kJ
R = 8.3 J/K/mol
And T = 600K
log(k₁k₂)=(41.9×1000)2.303×8.3×600 = 3.66
k₁k₂ = antilog(3.66)
=0.002