a) Calculate the equilibrium constant at 17 K for a reaction with ΔHrxno = 10 kJ and ΔSrxno = -100 J/K. (Don't round until the end. Using the exponent enlarges any round-off error.)
b) Calculate the equilibrium constant at 146 K for the thermodynamic data in the previous question (Notice that Keq is larger at the larger temperature for an endothermic reaction)
c) Calculate the equilibrium constant at 43 K for a reaction with ΔHrxno = 10 kJ and ΔSrxno = 100 J/K.
d) Calculate the equilibrium constant at 145 K for the
thermodynamic data in the previous question.
(Notice that Keq is dramatically larger for a larger
temperature when there is a substantial positive increase in
entropy.)
e) Using data from the Appendix, calculate ΔGo (in
kJ) at 65oC for the
reaction:
N2O(1 atm) + H2(1 atm) ↔ N2(1 atm)
+H2O(l) (Recall, all gases at 1 atm for standard
conditions)
f)Calculate ΔG (in kJ) at 65 oC for the
reaction:
N2O(0.0061 atm) + H2(0.25 atm) ↔
N2(445.4 atm) +H2O(l)
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