Consider the chemical reaction and thermochemical information
and initial partial pressures of the reaction components given
below:
CH3OH(g) + HBr(g) ⇌ CH3Br(g) +
H2O(g)
| ΔHf° (kJ/mol) | S° (J mol-1 K-1) | P (atm) | |||
| CH3Br | -35.50 | 246.40 | 0.462 | ||
| H2O | -241.83 | 188.84 | 0.984 | ||
| CH3OH | -201.50 | 239.80 | 5.82 | ||
| HBr | -36.29 | 198.70 | 5.22 |
Determine ΔG (in kJ) for this reaction at 867.29 K. Assume
ΔH°f and S° do not vary as a function of temperature.
Report your answer to two decimal places in standard notation (i.e.
123.45 kJ).
To determine ΔG (Gibbs free energy) for the given reaction at 867.29 K, we can use the equation:
ΔG = ΔH - TΔS
where ΔH is the change in enthalpy, T is the temperature in Kelvin, and ΔS is the change in entropy.
Given: ΔHf° (kJ/mol) and S° (J mol-1 K-1) for each component: CH3Br: ΔHf° = -35.50 kJ/mol, S° = 246.40 J mol-1 K-1 H2O: ΔHf° = -241.83 kJ/mol, S° = 188.84 J mol-1 K-1 CH3OH: ΔHf° = -201.50 kJ/mol, S° = 239.80 J mol-1 K-1 HBr: ΔHf° = -36.29 kJ/mol, S° = 198.70 J mol-1 K-1
The reaction can be written as: CH3OH(g) + HBr(g) ⇌ CH3Br(g) + H2O(g)
Now, let's calculate ΔG for the reaction using the given information:
ΔG = ΣΔGf°(products) - ΣΔGf°(reactants)
First, let's calculate the ΔGf° (standard Gibbs free energy change of formation) for each component:
ΔGf° (CH3Br) = ΔHf° (CH3Br) - TΔS° (CH3Br) = (-35.50 kJ/mol) - (867.29 K * (246.40 J/mol K / 1000)) = -35.50 kJ/mol - 214.19 kJ/mol = -249.69 kJ/mol
ΔGf° (H2O) = ΔHf° (H2O) - TΔS° (H2O) = (-241.83 kJ/mol) - (867.29 K * (188.84 J/mol K / 1000)) = -241.83 kJ/mol - 163.67 kJ/mol = -405.50 kJ/mol
ΔGf° (CH3OH) = ΔHf° (CH3OH) - TΔS° (CH3OH) = (-201.50 kJ/mol) - (867.29 K * (239.80 J/mol K / 1000)) = -201.50 kJ/mol - 207.06 kJ/mol = -408.56 kJ/mol
ΔGf° (HBr) = ΔHf° (HBr) - TΔS° (HBr) = (-36.29 kJ/mol) - (867.29 K * (198.70 J/mol K / 1000)) = -36.29 kJ/mol - 172.18 kJ/mol = -208.47 kJ/mol
Now, let's substitute these values into the equation to calculate ΔG:
ΔG = ΣΔGf°(products) - ΣΔGf°(reactants) = [ΔGf° (CH3Br) + ΔGf° (H2O)] - [ΔGf° (CH3OH) + ΔGf° (HBr)] = [-249.69 kJ/mol + (-405.50 kJ/mol)] - [-408.56 kJ/mol + (-208.47 kJ/mol)] = -655.19 kJ/mol + 616.03 kJ/mol = -39.16 kJ/mol
Consider the chemical reaction and thermochemical information and initial partial pressures of the reaction components given...
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I
wasn't given the partial pressures so why do you need it? can the
problem really not be solved without it?
1
bar for each
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