Heat of formation is the wrong thing to use. It refers to the formation of a compound from its elements.
The enthalpy of combustion of a mole of glucose to carbon dioxide and water is:
[tex] \Delta _{c}H^{ \Theta } \ = \ - 2808 \ \frac{kJ}{mol}[/tex]
I will do all the calculations necessary to determine the change of entropy of our reference system (the human body). To do that, I will assume that the standard enthalpy of combustion is equal to the heat transferred reversibly to our system.
[tex]q_{rev} \ = \ - 2808 \ \frac{kJ}{mol} \ \times \ 0.556 \ mol \ = \ - 1561.25 \ kJ[/tex]
Now that I know the value of q
rev, it's time to calculate the change of entropy.
[tex]\Delta S \ = \ \frac{q_{rev}}{T} \ = \ \frac{1561.25 \ kJ}{310 \ K} \ \approx \ 5.03 \frac{kJ}{K}[/tex]
The heat transferred, by convention, is positive. It's because heat enters the system.
Thanks for helping me out.
Or, ironically, it can be calculated from heats of formation.
I already used the standard enthalpy of formation of a mole of glucose from its elemental constituents but the answer doesn't correspond to the one written in my book.
Or probably you're talking about applying Hess's Law? I'm still struggling about applying Hess's Law. I tried using it to solve this problem, but I'm having difficulty applying it. I can't tell whether I'm doing it right or I'm making mistakes.
What I would do if I used Hess's Law:C
6H
12O
6(s) 6C
(s) + 6H
2(g) + 3O
2(g) Δ
fH = + 1273 kJ/mol
6C
(s) + 6O
2(g) 6CO
2(g) Δ
fH = - 6(393.51) kJ/mol
6H
2(g) + 3O
2(g) 6H
2O
(l) Δ
fH = - 3(241.818) kJ/mol
Then I would stop here, because the sum of the enthalpies isn't equal to the standard enthalpy of combustion of glucose. Plus, I still have to review Hess's Law...