The Arrhenius Equation gives:
#sf(k=Ae^(-E_a/(RT)))#
#sf(k)# is the rate constant
#sf(A)# is the frequency factor, which is constant for a particular reaction
#sf(R)# is the gas constant, #sf(8.31"J/K/mol")#
#sf(T)# is the absolute temperature
Taking natural logs:
#sf(lnk=lnA-E_a/(RT))#
If #sf(T_1=800color(white)(x)K)# and #sf(T_2=700color(white)(x)K)# then:
#sf(lnk_1=lnA-E_a/(RT_1)" "color(red)((1)))#
and
#sf(lnk_2=lnA-E_a/(RT_2)" "color(red)((2))#
Subtracting both sides of #sf(color(red)((1)))# from #sf(color(red)((2))rArr#
#sf(ln[k_1/k_2]=-E_a/(RT_1)-(-E_a/(RT_2)))#
#:.##sf(ln[k_1/k_2]=E_a/R[1/T_2-1/T_1])#
Putting in the numbers:
#sf(ln[k_1/k_2]=(315xx10^3)/(8.31)[1/700-1/800])#
#sf(ln[k_1/k_2]=6.747)#
#:.##sf(k_1/k_2=851.728)#
#:.##sf(k_2=(9.7xx10^10)/851.728=1.1xx10^(8)color(white)(x)l.mol^(-1).s^(-1))#
This is less than #sf(k_1)# which is what you would expect since the reaction occurs at a lower temperature.