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In a 7.0 Levacuated chamber, 0.50 mol H(...

In a 7.0 Levacuated chamber, 0.50 mol `H_(2)` and 0.50 mol `I_(2)` react at `427^(@)` C.
`H_(2) (g) + I_(2) (g) hArr HI (g) ` + Heat , At the given temperature, `K_(c)` = 49 for the reaction.
What is the total pressure (atm) in the chamber ?

A

83.14

B

831.4

C

8.21

D

None of these

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem, we will follow these steps: ### Step 1: Write the balanced chemical equation The balanced chemical reaction is: \[ \text{H}_2(g) + \text{I}_2(g) \rightleftharpoons 2\text{HI}(g) + \text{Heat} \] ### Step 2: Set up the initial concentrations Initially, we have: - Moles of \( \text{H}_2 = 0.50 \) mol - Moles of \( \text{I}_2 = 0.50 \) mol - Moles of \( \text{HI} = 0 \) mol ### Step 3: Define the change in moles at equilibrium Let \( x \) be the moles of \( \text{H}_2 \) and \( \text{I}_2 \) that react at equilibrium. Thus, at equilibrium: - Moles of \( \text{H}_2 = 0.50 - x \) - Moles of \( \text{I}_2 = 0.50 - x \) - Moles of \( \text{HI} = 2x \) ### Step 4: Write the expression for \( K_c \) The equilibrium constant \( K_c \) is given by: \[ K_c = \frac{[\text{HI}]^2}{[\text{H}_2][\text{I}_2]} \] Substituting the equilibrium concentrations: \[ K_c = \frac{(2x)^2}{(0.50 - x)(0.50 - x)} = 49 \] ### Step 5: Solve for \( x \) Expanding the equation: \[ \frac{4x^2}{(0.50 - x)^2} = 49 \] Cross-multiplying gives: \[ 4x^2 = 49(0.50 - x)^2 \] Expanding the right side: \[ 4x^2 = 49(0.25 - x + x^2) \] \[ 4x^2 = 12.25 - 49x + 49x^2 \] Rearranging the equation: \[ 0 = 45x^2 - 49x + 12.25 \] ### Step 6: Use the quadratic formula to find \( x \) Using the quadratic formula \( x = \frac{-b \pm \sqrt{b^2 - 4ac}}{2a} \): - \( a = 45 \) - \( b = -49 \) - \( c = 12.25 \) Calculating the discriminant: \[ D = (-49)^2 - 4 \times 45 \times 12.25 = 2401 - 2205 = 196 \] Thus: \[ x = \frac{49 \pm \sqrt{196}}{2 \times 45} = \frac{49 \pm 14}{90} \] Calculating the two possible values for \( x \): 1. \( x = \frac{63}{90} = 0.7 \) (not possible since it exceeds initial moles) 2. \( x = \frac{35}{90} \approx 0.39 \) ### Step 7: Calculate equilibrium concentrations Substituting \( x \) back: - Moles of \( \text{H}_2 = 0.50 - 0.39 = 0.11 \) - Moles of \( \text{I}_2 = 0.50 - 0.39 = 0.11 \) - Moles of \( \text{HI} = 2(0.39) = 0.78 \) ### Step 8: Calculate total moles at equilibrium Total moles at equilibrium: \[ n_{total} = 0.11 + 0.11 + 0.78 = 1.0 \text{ mol} \] ### Step 9: Calculate total pressure using the ideal gas law Using the ideal gas law \( PV = nRT \): - \( P = \frac{nRT}{V} \) - \( R = 0.0821 \, \text{atm L/(mol K)} \) - \( T = 427 + 273 = 700 \, K \) - \( V = 7.0 \, L \) Calculating pressure: \[ P = \frac{(1.0 \, \text{mol})(0.0821 \, \text{atm L/(mol K)})(700 \, K)}{7.0 \, L} \] \[ P = \frac{57.47}{7.0} \approx 8.21 \, \text{atm} \] ### Step 10: Conclusion The total pressure in the chamber at equilibrium is approximately: \[ \text{Total Pressure} \approx 8.21 \, \text{atm} \]
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