Question #079ac
1 Answer
I got
DISCLAIMER: LONG ANSWER!
The basic idea is that since enthalpy is a state function, you can focus on the initial and final states of the system. It does not depend on the path you take.
Hess's Law is based off of this property of enthalpy, and states that you can:
- Reverse a reaction --- this switches the sign of
DeltaH for that reaction. - Scale a reaction by a constant (e.g.
1/2 ,3 , etc) --- this multipliesDeltaH for that reaction by the number you used.
So, what you should do for these problems is try to make your intermediates and/or catalysts cancel.
PROBLEM 4
Overall reaction:
"Ca"(s) + 2"H"_2"O"(l) -> "Ca"("OH")_2(s) + "H"_2(g)
Unmodified component reactions:
(1):
" H"_2(g) + 1/2"O"_2(g) -> "H"_2"O"(l)
DeltaH = -"285 kJ/mol" (2):
" CaO"(s) + "H"_2"O"(l) -> "Ca"("OH")_2(s)
DeltaH = -"64 kJ/mol" (3):
" Ca"(s) + 1/2"O"_2(g) -> "CaO"(s)
DeltaH = -"635 kJ/mol"
- Since
"Ca"(s) is a reactant in the overall reaction with a stoichiometric coefficient of1 , we can use (3) as-is. - Since
"H"_2(g) is a product in the overall reaction with a stoichiometric coefficient of1 , we can reverse (1) and then use it like that. - Since
"Ca"("OH")_2(s) is a product in the overall reaction with a stoichiometric coefficient of1 , we can use (2) as-is.
Everything else cancels out accordingly.
Modified component reactions:
\mathbf(-) (1):" H"_2"O"(l) -> "H"_2(g) + cancel(1/2"O"_2(g)) ,DeltaH = -(-"285 kJ/mol") = color(red)(+"285 kJ/mol") (2):
cancel("CaO"(s)) + "H"_2"O"(l) -> "Ca"("OH")_2(s) ,DeltaH = -"64 kJ/mol" (3):
" Ca"(s) + cancel(1/2"O"_2(g)) -> cancel("CaO"(s)) ,DeltaH = -"635 kJ/mol"
"---------------------------------------------------------"
\mathbf("Ca"(s) + 2"H"_2"O"(l) -> "Ca"("OH")_2(s) + "H"_2(g))
= (+"285 kJ/mol") + (-"64 kJ/mol") + (-"635 kJ/mol")
= color(blue)(-"414 kJ/mol")
PROBLEM 5 (the units of
Overall reaction:
"FeO"(s) + "CO"(g) -> "Fe"(s) + "CO"_2(g)
Unmodified component reactions:
(1):
" 3Fe"_2"O"_3(s) + "CO"(g) -> 2"Fe"_3"O"_4(s) + "CO"_2(g)
DeltaH = -"47 kJ/mol"
(2):" Fe"_2"O"_3(s) + 3"CO"(g) -> 2"Fe"(s) + 3"CO"_2(g)
DeltaH = -"25 kJ/mol"
(3):" Fe"_3"O"_4(s) + "CO"(g) -> 3"FeO"(s) + "CO"_2(g)
DeltaH = +"19 kJ/mol"
- Since
"FeO"(s) is a reactant in the overall reaction with a stoichiometric coefficient of1 , but it is a product in (3) with a stoichiometric coefficient of3 , we must scale (3) by1/3 and reverse it. - Since
"Fe"(s) is a product in the overall reaction with a stoichiometric coefficient of1 , but it is a product in (2) with a stoichiometric coefficient of2 , we have to scale (2) by1/2 . - For
"CO"_2 after modifying (2) and (3), we will have1/3"CO"_2 as reactants and3/2"CO"_2 as products, and in the overall reaction we have1"CO"_2 as products. Right now, this will cancel as3/2 - 1/3 = 9/6 - 2/6 = 7/6"CO"_2 as products. Since in the overall reaction, there is only one"CO"_2 , we need to scale (1) by1/6 and reverse it so that7/6 - 1/6 = 6/6 = 1"CO"_2 on the reactants side.
Everything else cancels out accordingly. For each reactant, I've converted the fractions to common denominators for you, but you will have to do it yourself on a test.
Modified component reactions:
\mathbf(-1/6) (1):cancel(1/3"Fe"_3"O"_4(s)) + 1/6"CO"_2(g) -> cancel(1/2"Fe"_2"O"_3(s)) + 1/6"CO"(g) ,DeltaH = -1/6(-"47 kJ/mol") = color(red)(+7.8bar(33)) color(red)("kJ/mol")
\mathbf(1/2) (2):cancel(1/2"Fe"_2"O"_3(s)) + 9/6"CO"(g) -> "Fe"(s) + 9/6"CO"_2(g) ,DeltaH = 1/2(-"25 kJ/mol") = -color(red)("12.5") color(red)("kJ/mol")
\mathbf(-1/3) (3):"FeO"(s) + 2/6"CO"_2(g) -> cancel(1/3"Fe"_3"O"_4(s)) + 2/6"CO"(g) ,DeltaH = -1/3(+"19 kJ/mol") = color(red)(-6.bar(33)) color(red)("kJ/mol")
"---------------------------------------------------------"
\mathbf("FeO"(s) + "CO"(g) -> "Fe"(s) + "CO"_2(g))
= (+"7.8"bar(33) "kJ/mol") + (-"12.5 kJ/mol") + (-6.bar(33) "kJ/mol")
= color(blue)(-"11 kJ/mol")