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In an experiment, 8.0 moles of H2(g) is heated with 5.0 moles of I2(g) in a closed vessel at 298 K. At equilibrium, 9.06 mol of hydrogen iodide are formed. Calculate the equilibrium constants Kc and Kp at that temperature (R = 8.314 J mol-1 or 0.082 atm dm3 K-1 mol-1).

Chemistry

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Answer

50.3\text{50.3}

Step-by-step solution

5 steps
  1. Write the balanced chemical equation and set up an ICE table for moles.

    The reaction is between hydrogen gas and iodine gas to form hydrogen iodide gas.

    H2(g)+I2(g)⇌2HI(g)\text{H}_2\text{(g)} + \text{I}_2\text{(g)} \rightleftharpoons 2\text{HI(g)}

    Initial moles: H2=8.0 mol\text{H}_2 = 8.0 \text{ mol}, I2=5.0 mol\text{I}_2 = 5.0 \text{ mol}, HI=0 mol\text{HI} = 0 \text{ mol}.
    Let xx be the moles of H2\text{H}_2 and I2\text{I}_2 that react. According to the stoichiometry, 2x2x moles of HI\text{HI} will be formed.

    SpeciesInitial (mol)Change (mol)Equilibrium (mol)
    H2\text{H}_28.0−x-x8.0−x8.0 - x
    I2\text{I}_25.0−x-x5.0−x5.0 - x
    HI\text{HI}0+2x+2x2x2x
  2. Calculate the value of xx using the given equilibrium moles of HI\text{HI}.

    At equilibrium, 9.06 mol9.06 \text{ mol} of hydrogen iodide (HI\text{HI}) are formed.
    So, 2x=9.06 mol2x = 9.06 \text{ mol}.

    x=9.062=4.53 molx = \frac{9.06}{2} = 4.53 \text{ mol}
  3. Calculate the equilibrium moles of all species.

    Equilibrium moles of H2=8.0−x=8.0−4.53=3.47 mol\text{H}_2 = 8.0 - x = 8.0 - 4.53 = 3.47 \text{ mol}
    Equilibrium moles of I2=5.0−x=5.0−4.53=0.47 mol\text{I}_2 = 5.0 - x = 5.0 - 4.53 = 0.47 \text{ mol}
    Equilibrium moles of HI=9.06 mol\text{HI} = 9.06 \text{ mol}

  4. Calculate the equilibrium constant KcK_c.

    The expression for KcK_c is:

    Kc=[HI]2[H2][I2]K_c = \frac{[\text{HI}]^2}{[\text{H}_2][\text{I}_2]}

    Let the volume of the closed vessel be V dm3V \text{ dm}^3. The concentrations are moles divided by volume.

    [H2]=3.47V mol/dm3[\text{H}_2] = \frac{3.47}{V} \text{ mol/dm}^3 [I2]=0.47V mol/dm3[\text{I}_2] = \frac{0.47}{V} \text{ mol/dm}^3 [HI]=9.06V mol/dm3[\text{HI}] = \frac{9.06}{V} \text{ mol/dm}^3

    Substitute these into the KcK_c expression:

    Kc=(9.06V)2(3.47V)(0.47V)=(9.06)2V2(3.47)(0.47)V2K_c = \frac{\left(\frac{9.06}{V}\right)^2}{\left(\frac{3.47}{V}\right)\left(\frac{0.47}{V}\right)} = \frac{\frac{(9.06)^2}{V^2}}{\frac{(3.47)(0.47)}{V^2}}

    The volume V2V^2 terms cancel out:

    Kc=(9.06)2(3.47)(0.47)=82.08361.6309K_c = \frac{(9.06)^2}{(3.47)(0.47)} = \frac{82.0836}{1.6309} Kc≈50.33K_c \approx 50.33

    Rounding to three significant figures, Kc=50.3K_c = \boxed{\text{50.3}}.

  5. Calculate the equilibrium constant KpK_p.

    The relationship between KpK_p and KcK_c is given by Kp=Kc(RT)ΔnK_p = K_c(RT)^{\Delta n}.
    Δn\Delta n is the change in the number of moles of gaseous products minus the number of moles of gaseous reactants.
    For the reaction H2(g)+I2(g)⇌2HI(g)\text{H}_2\text{(g)} + \text{I}_2\text{(g)} \rightleftharpoons 2\text{HI(g)}:
    Moles of gaseous products = 2 (from 2HI)
    Moles of gaseous reactants = 1 (from H2\text{H}_2) + 1 (from I2\text{I}_2) = 2
    So, Δn=2−2=0\Delta n = 2 - 2 = 0.
    Since Δn=0\Delta n = 0, (RT)Δn=(RT)0=1(RT)^{\Delta n} = (RT)^0 = 1.
    Therefore, Kp=Kc×1=KcK_p = K_c \times 1 = K_c.

    Kp=50.33K_p = 50.33

    Rounding to three significant figures, Kp=50.3K_p = \boxed{\text{50.3}}.

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