The rate "k" of a chemical reaction dependence on the absolute temperature "T" is described by Arrhenius law:
"k = A\u00b7e^{-\\frac{E_a}{RT}}" ,
where "A" is the pre-exponential factor, "E_a" is the activation energy and "R" is the universal gas constant.
The two measurements of the rate constants at two different temperatures are enough to calculate the values of the pre-exponential factor and of the activation energy:
"k_1 = A\u00b7e^{-\\frac{E_a}{RT_1}}"
"k_2 = A\u00b7e^{-\\frac{E_a}{RT_2}}"
"\\text{ln}(\\frac{k_1}{k_2}) = \\frac{E_a}{R}(\\frac{1}{T_2} - \\frac{1}{T_1})"
"E_a = R\u00b7\\frac{\\text{ln}(\\frac{k_1}{k_2})}{\\frac{1}{T_2} - \\frac{1}{T_1}}" .
The value of (1/T2−1/T1) is:
"\\frac{1}{T_2} - \\frac{1}{T_1} = \\frac{1}{273.15+37.0} - \\frac{1}{273.15+25.0} = -1.30\u00b710^{-4}" K-1.
The value of "\\text{ln}(\\frac{k_1}{k_2})" is:
"\\text{ln}(\\frac{k_1}{k_2}) = \\text{ln}(\\frac{0.100}{3.00}) = -3.40" .
Therefore, the activation energy is:
"E_a = 8.314 \\text{ (J\/(mol K)})\u00b7\\frac{-3.40}{-1.30\u00b710^{-4} (\\text{K}^{-1})}"
"E_a = 2.18\u00b710^5" J/mol, or 218 kJ/mol.
Answer: The value of (1/T2−1/T1) is -1.30·10-4 K-1.
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