At 320 K, a gas `A_(2)` is 20% dissociated to A(g). The standard free energy change at 320 K and 1 atm in `J mol^(-1)` is approximately : `(R =8.314 Jk^(-1)"mol"^(-1), "In" 2=0.693, "In" 3 = 1.098)`
A
1844
B
4763
C
2068
D
4281
Text Solution
AI Generated Solution
The correct Answer is:
To find the standard free energy change (ΔG) for the dissociation of gas A₂ at 320 K and 1 atm, we can follow these steps:
### Step 1: Determine the initial and final amounts of A₂ and A
Initially, we have 1 mole of A₂. Since A₂ is 20% dissociated, the amount of A₂ that dissociates is:
\[
\text{Amount dissociated} = 20\% \text{ of } 1 \text{ mole} = 0.2 \text{ moles}
\]
Thus, the amount of A formed is:
\[
\text{Amount of A} = 2 \times 0.2 = 0.4 \text{ moles}
\]
After dissociation, the amounts are:
- A₂ remaining: \(1 - 0.2 = 0.8 \text{ moles}\)
- A formed: \(0.4 \text{ moles}\)
### Step 2: Calculate the equilibrium constant (Kp)
The equilibrium constant for the reaction \(A_2(g) \rightleftharpoons 2A(g)\) can be expressed as:
\[
K_p = \frac{(P_A)^2}{(P_{A_2})}
\]
Where:
- \(P_A\) is the partial pressure of A
- \(P_{A_2}\) is the partial pressure of A₂
Assuming ideal gas behavior and that the total pressure is 1 atm, we can express the partial pressures:
\[
P_{A_2} = \frac{0.8}{1} \text{ atm} = 0.8 \text{ atm}
\]
\[
P_A = \frac{0.4}{1} \text{ atm} = 0.4 \text{ atm}
\]
Thus:
\[
K_p = \frac{(0.4)^2}{0.8} = \frac{0.16}{0.8} = 0.2
\]
### Step 3: Calculate ΔG using the formula
The standard free energy change (ΔG) is calculated using the formula:
\[
\Delta G = -RT \ln K_p
\]
Where:
- \(R = 8.314 \text{ J K}^{-1} \text{ mol}^{-1}\)
- \(T = 320 \text{ K}\)
- \(K_p = 0.2\)
Substituting the values:
\[
\Delta G = -8.314 \times 320 \times \ln(0.2)
\]
### Step 4: Calculate ln(0.2)
Using the properties of logarithms:
\[
\ln(0.2) = \ln\left(\frac{2}{10}\right) = \ln(2) - \ln(10)
\]
Given that \(\ln(2) = 0.693\) and \(\ln(10) \approx 2.303\):
\[
\ln(0.2) = 0.693 - 2.303 = -1.610
\]
### Step 5: Substitute ln(0.2) back into the ΔG equation
Now substituting back into the ΔG equation:
\[
\Delta G = -8.314 \times 320 \times (-1.610)
\]
Calculating this gives:
\[
\Delta G = 8.314 \times 320 \times 1.610 \approx 4281 \text{ J mol}^{-1}
\]
### Final Answer
The standard free energy change at 320 K and 1 atm is approximately:
\[
\Delta G \approx 4281 \text{ J mol}^{-1}
\]
The standard free energy change of a reaction is DeltaG^(@)=-kJ//mol^(-1) at 298 K. Calculate the value of log_(10)K_(p) (R=8.314JK^(-1)mol^(-1))
The rate temperature changes from 300K to 310K. Activation energy of such a reaction will be (R = 8.314 JK^(-1) mol^(-1) " and " log 2 = 0.3010)
Calculate the total and average kinetic energy of 32 g of methane molecules at 27^(@)C. (R="8.314 J K"^(-1)"mol"^(-1)) .
The standard free energy change of a reaction is DeltaG^(@)=-115 at 298K. Calculate the equilibrium constant K_(P) in log K_(P).(R=8.314JK^(-1)mol^(-1))
The rate of a reaction doubles when the tempeature changes from 300 K to 310 K. Activation energy for the reaction is: (R = 8.314 JK^(-1) mol^(-1), log2 = 0.3010)
The kinetic energy of two moles of N_(2) at 27^(@) C is (R = 8.314 J K^(-1) mol^(-1))