Question #d10dd
1 Answer
This is just asking you to use the Arrhenius equation. In fact, it takes you through every major step.
#k = Ae^(-E_a//RT)#
#k# is the rate constant at some temperature#T# in#"K"# .#A# is the frequency factor in#"s"^(-1)# .#E_a# is the activation energy.#R# is the universal gas constant.
Given two temperatures, one can obtain the
#k_1 = Ae^(-E_a//RT_1)#
#k_2 = Ae^(-E_a//RT_2)#
And one can readily see that taking the ratio is useful.
#k_1/k_2 = e^(-E_a/(RT_1) + E_a/(RT_2))#
And so,
#ln(k_1/k_2) = -E_a/(RT_1) + E_a/(RT_2)#
#= E_a/R[1/T_2 - 1/T_1]#
is the
This is simple enough; convert temperature from
#""^@ "C"# to#"K"# and plug them in.
#25^@ "C" + 273.15 = "298.15 K"#
#43^@ "C" + 273.15 = "316.15 K"# Therefore:
#1/T_2 - 1/T_1 = [1/316.15 - 1/298.15] "K"^(-1)#
#= -"0.0001910 K"^(-1)#
The left-hand side is then:
#ln(k_1/k_2) = ln(0.100/2.70)#
#= -3.296#
And so the activation energy is:
#color(blue)(E_a) = Rln(k_1/k_2) cdot [1/T_2 - 1/T_1]^(-1)#
#= "0.008314472 kJ/mol"cdotcancel"K" cdot (-3.296) cdot 1/(-0.0001910) cancel"K"#
#=# #color(blue)("143.48 kJ/mol")# And this corresponds to an ordinary reaction rate.