Arrhenius equation for calculation of rate constant at different temperatures is given by
K=A e−Ea/RT
where,
K= rate constant at temperature TK
A= Arrhenius constant
Ea= activation energy of the reaction
R= universal gas constant
T= temperature in K
Let, us suppose, at temperature T,K and T2K the rate constants are K1 and K2 respectively,so,
K1=A e−Ea/RT1 −(i)
K2=A e−Ea/RT22 −(ii)
(ii)/(i)
⇒K2K1=e−Ea/RT2e−Ea/Rt1
Taking log on both sides:-
⇒log(K2K1)=log⎛⎜⎝e−EaR(1T2−1T1)⎞⎟⎠
⇒logK2K1=EaR(1T1−1T2)
Now, according to question,
T1=600K, K1=1.60×106s−1
K2=?, T2=700K, Ea=2.209×103 J/mol
R=8.314 JK−1mol−1
⇒log(K2K1)=+22098.314[1600−1700]
⇒log(K2K1)=2209×10083140×6×7
⇒log(K21.6×106)=0.63
Taking antilog on both sides:-
⇒K21.6×106= Antilog(0.63)
⇒K2=1.87×1.6×106
⇒K2=3×106s−1