1. Keq = 8.63x10-4 for a reaction. Which of the following must be true?
∆Gº=0 | |
∆Gº=1 | |
∆Gº>0 | |
∆Gº<0 |
2. What is the value of Keq if ∆Gº=-9.48 kJ (R=8.314 J/mol-K)?
6700 | |
1.00 | |
1.01 | |
45.9 |
3. Calculate ∆Gº for the reaction, C3H8(g)+5O2(g)→3CO2(g)+4H2O(g), where ∆Gfº=-23.5 kJ/mol for CH4(g), -394 kJ/mol for CO2(g), and -229 kJ/mol for H2O(g):
600 kJ | |
-600 kJ | |
-2070 kJ | |
2070 kJ |
1.
Keq= 8.63x10^-4
G0 = - RT
lnKeq
Keq is a positive value
G0 getting the
negative value
So, G0 is less than
zero
G0<0
The answer is D
2)
G0 = - 9.48
KJ
R= 8.314 J/mol-k
T = 25C = 25+273=298K
G0 = - RT
lnKeq
- 9.48x10^3 = - 8.314x273xlnKeq
lnKeq = 3.826
Keq= e^3.826
Keq= 45.88
Keq= 45.9
3)
C3H8(g) + 5O2(g) → 3CO2(g) + 4H2O(g
G0rxn = [
3x
G0f of CO2 +
4x
G0f of H2O] - [
G0f of C3H8 +
5x
G0f of O2]
G0rxn =[ 3 x( -
394) + 4x( -229)] - [ - 23.5 + 5 x 0.0]
G0rxn = - 2074.5
KJ
according to the given values the answer is
G0rxn = - 2074.5
KJ
(OR)
The answer is C
1. Keq = 8.63x10-4 for a reaction. Which of the following must be true? ∆Gº=0 ∆Gº=1...
Calculate ∆Gº for the reaction, CH4(g)+2O2(g)→CO2(g)+2H2O(g), where ∆Gfº=-50.8 kJ/mol for CH4(g), -394 kJ/mol for CO2(g), and -229 kJ/mol for H2O(g).
Calculate ∆Gº for the reaction, CH4(g)+2O2(g)→CO2(g)+2H2O(g), where ∆Gfº=-50.8 kJ/mol for CH4(g), -394 kJ/mol for CO2(g), and -229 kJ/mol for H2O(g): 572 kJ -801 kJ -572 kJ 801 kJ
2. Given the following reaction: 2CH2OH(g) + 302(g) → 2CO2(g) + 4H2O(g) Delta Gº Kj/mol -163 CH2OH O, CO2 H20 -394 -229 What is Delta G for the reaction
Keq = 127 for a reaction. Which of the following must be true? ∆Gº>0 ∆Gº=1 ∆Gº=0 ∆Gº<0
Imagine that a chemist puts 6.40 mol each of C3H8 and O2 in a 1.00-L container at constant temperature of 289 °C. This reaction occurs: C3H8(g) + 5O2(g) ⇄ 3CO2(g) + 4H2O(g) When equilibrium is reached, 0.411 mol of CO2 is in the container. Find the value of Keq for the reaction.
Calculate
rxn for the below combustion reaction, determine if
entropy increases or decreases. Assume 1 mol of substance at 25
Celsius.
C3H8(g) + 5O2(g)
3CO2(g) + 4H2O(l)
Delta G of C3H8 = -23.4 kj/mol
Delta G of O2 = 0 kj/mol
Delta G of CO2 = -394.36 kj/mol
Delta G of H2O = -237.1 kj/mol
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The combustion of propane, C3H8, occurs via the reaction C3H8(g)+5O2(g)→3CO2(g)+4H2O(g) with heat of formation values given by the following table: Substance ΔH∘f (kJ/mol) C3H8 (g)= -104.7 CO2(g)= −393.5 H2O(g)= −241.8 Calculate the enthalpy for the combustion of 1 mole of propane.
Use Hess's law to determine A.Hº for the reaction C3H4(g) + 2 H2(g) -> C3H8(8), given that Hy(8) + O2(8) — H2O(1) A Hº = -285.8 kJ mol-1 C3H4(8) + 402(g) — 3 CO2(g) + 2 H2O(1) A Hº = -1937 kJ mol-1 C3H2(g) + 5O2(g) — 3CO2(g) + 4H2O(1) A Hº = -2219.1 kJ mol-1
20.5)
Calculate ΔGo for the reaction
SiCl4(g) 2Mg(s) 2MgCl2(s) Si(s)
Substance SiCl4 Mg(s) MgCl2(s) Si(s)
ΔGof(kJ/mol) -616.98 0 -591.79 0
a)566.60kJ
b)50.38kJ
c)25.19kJ
d)- 25.19kJ
e)- 566.60kJ
Calculate Delta So for the combustion of propane. C3H8(g) + 5O2(g) rightarrow 3CO2(g)+4H2O(g) Sustance C3H8 O2 CO2 H2O So(J/k.mol) 269.9 205.138 213.74 188.825
Propane (C3H8)burns according to the following balanced equation: C3H8(g)+5O2(g)→3CO2(g)+4H2O(g) Calculate ΔH∘rxnΔ for this reaction using standard enthalpies of formation. (The standard enthalpy of formation of gaseous propane is -103.9 kJ/molkJ/mol.) Express the enthalpy in kilojoules to four significant figures.