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A 5.0 g of an impure iron reacted completely with 750 cm³ of 2.0 mol dm⁻³ hydrochloric acid to give a neutral solution. Calculate the percentage purity of the sample of iron

Chemistry

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Here are the answers to question 5:

a) (i) Hess's Law of constant heat summation states that the total enthalpy change for a chemical reaction is independent of the pathway taken, provided the initial and final conditions are the same. In other words, if a reaction can be expressed as a sum of several steps, the enthalpy change for the overall reaction is the sum of the enthalpy changes for each step.

a) (ii) We want to calculate ΔH\Delta H for the reaction:

C2H4(g)+H2(g)→C2H6(g)\text{C}_2\text{H}_{4(g)} + \text{H}_{2(g)} \rightarrow \text{C}_2\text{H}_{6(g)}

Given the following reactions:

  1. C2H4(g)+3O2(g)→2CO2(g)+2H2O(l)\text{C}_2\text{H}_{4(g)} + 3\text{O}_{2(g)} \rightarrow 2\text{CO}_{2(g)} + 2\text{H}_2\text{O}_{(l)}; ΔH1=−1411 kJ mol−1\Delta H_1 = -1411 \text{ kJ mol}^{-1}
  2. C2H6(g)+72O2(g)→2CO2(g)+3H2O(l)\text{C}_2\text{H}_{6(g)} + \frac{7}{2}\text{O}_{2(g)} \rightarrow 2\text{CO}_{2(g)} + 3\text{H}_2\text{O}_{(l)}; ΔH2=−1560 kJ mol−1\Delta H_2 = -1560 \text{ kJ mol}^{-1}
  3. H2(g)+12O2(g)→H2O(l)\text{H}_{2(g)} + \frac{1}{2}\text{O}_{2(g)} \rightarrow \text{H}_2\text{O}_{(l)}; ΔH3=−1411 kJ mol−1\Delta H_3 = -1411 \text{ kJ mol}^{-1}
  1. Manipulate the given equations to match the target equation.

    • Reaction 1 has C2H4(g)\text{C}_2\text{H}_{4(g)} on the reactant side, as required. Keep it as is. C2H4(g)+3O2(g)→2CO2(g)+2H2O(l)\text{C}_2\text{H}_{4(g)} + 3\text{O}_{2(g)} \rightarrow 2\text{CO}_{2(g)} + 2\text{H}_2\text{O}_{(l)}; ΔH1=−1411 kJ mol−1\Delta H_1 = -1411 \text{ kJ mol}^{-1}

    • Reaction 3 has H2(g)\text{H}_{2(g)} on the reactant side, as required. Keep it as is. H2(g)+12O2(g)→H2O(l)\text{H}_{2(g)} + \frac{1}{2}\text{O}_{2(g)} \rightarrow \text{H}_2\text{O}_{(l)}; ΔH3=−1411 kJ mol−1\Delta H_3 = -1411 \text{ kJ mol}^{-1}

    • Reaction 2 has C2H6(g)\text{C}_2\text{H}_{6(g)} on the reactant side, but it needs to be on the product side. Reverse reaction 2 and change the sign of its ΔH\Delta H. 2CO2(g)+3H2O(l)→C2H6(g)+72O2(g)2\text{CO}_{2(g)} + 3\text{H}_2\text{O}_{(l)} \rightarrow \text{C}_2\text{H}_{6(g)} + \frac{7}{2}\text{O}_{2(g)}; ΔH2′=−(−1560)=+1560 kJ mol−1\Delta H_2' = -(-1560) = +1560 \text{ kJ mol}^{-1}

  2. Sum the manipulated equations and their enthalpy changes.

    Add the three modified reactions:
    C2H4(g)+3O2(g)+H2(g)+12O2(g)+2CO2(g)+3H2O(l)→2CO2(g)+2H2O(l)+H2O(l)+C2H6(g)+72O2(g)\text{C}_2\text{H}_{4(g)} + 3\text{O}_{2(g)} + \text{H}_{2(g)} + \frac{1}{2}\text{O}_{2(g)} + 2\text{CO}_{2(g)} + 3\text{H}_2\text{O}_{(l)} \rightarrow 2\text{CO}_{2(g)} + 2\text{H}_2\text{O}_{(l)} + \text{H}_2\text{O}_{(l)} + \text{C}_2\text{H}_{6(g)} + \frac{7}{2}\text{O}_{2(g)}

  3. Cancel common species on both sides of the equation.

    • 2CO2(g)2\text{CO}_{2(g)} on both sides cancel out.
    • 3H2O(l)3\text{H}_2\text{O}_{(l)} on the left (2H2O(l)+H2O(l)2\text{H}_2\text{O}_{(l)} + \text{H}_2\text{O}_{(l)}) cancel out with 3H2O(l)3\text{H}_2\text{O}_{(l)} on the right.
    • 3O2(g)+12O2(g)=72O2(g)3\text{O}_{2(g)} + \frac{1}{2}\text{O}_{2(g)} = \frac{7}{2}\text{O}_{2(g)} on the left, which cancels out with 72O2(g)\frac{7}{2}\text{O}_{2(g)} on the right.

    The resulting equation is:
    C2H4(g)+H2(g)→C2H6(g)\text{C}_2\text{H}_{4(g)} + \text{H}_{2(g)} \rightarrow \text{C}_2\text{H}_{6(g)}

  4. Calculate the total enthalpy change.

    ΔHreaction=ΔH1+ΔH3+ΔH2′\Delta H_{\text{reaction}} = \Delta H_1 + \Delta H_3 + \Delta H_2'
    ΔHreaction=(−1411 kJ mol−1)+(−1411 kJ mol−1)+(+1560 kJ mol−1)\Delta H_{\text{reaction}} = (-1411 \text{ kJ mol}^{-1}) + (-1411 \text{ kJ mol}^{-1}) + (+1560 \text{ kJ mol}^{-1})
    ΔHreaction=−2822 kJ mol−1+1560 kJ mol−1\Delta H_{\text{reaction}} = -2822 \text{ kJ mol}^{-1} + 1560 \text{ kJ mol}^{-1}
    ΔHreaction=−1262 kJ mol−1\Delta H_{\text{reaction}} = -1262 \text{ kJ mol}^{-1}

    ΔH=−1262 kJ mol−1\boxed{\Delta H = -1262 \text{ kJ mol}^{-1}}

    b) A 5.0 g5.0 \text{ g} of an impure iron reacted completely with 750 cm3750 \text{ cm}^3 of 2.0 mol dm−32.0 \text{ mol dm}^{-3} hydrochloric acid to give a neutral solution. Calculate the percentage purity of the sample of iron.
    (Assume the reaction is Fe(s)+2HCl(aq)→FeCl2(aq)+H2(g)\text{Fe}(s) + 2\text{HCl}(aq) \rightarrow \text{FeCl}_2(aq) + \text{H}_2(g))
    Molar mass of Fe = 55.845 g/mol55.845 \text{ g/mol} (approximately 56 g/mol56 \text{ g/mol} for WASSCE)

  5. Calculate the moles of HCl\text{HCl} used.

    Volume of HCl=750 cm3=0.750 dm3\text{HCl} = 750 \text{ cm}^3 = 0.750 \text{ dm}^3
    Concentration of HCl=2.0 mol dm−3\text{HCl} = 2.0 \text{ mol dm}^{-3}
    Moles of HCl=Concentration×Volume\text{HCl} = \text{Concentration} \times \text{Volume}
    Moles of HCl=2.0 mol dm−3×0.750 dm3=1.5 mol\text{HCl} = 2.0 \text{ mol dm}^{-3} \times 0.750 \text{ dm}^3 = 1.5 \text{ mol}

  6. Determine the moles of pure iron reacted using the stoichiometry of the reaction.

    From the balanced equation: Fe(s)+2HCl(aq)→FeCl2(aq)+H2(g)\text{Fe}(s) + 2\text{HCl}(aq) \rightarrow \text{FeCl}_2(aq) + \text{H}_2(g)
    The mole ratio of Fe:HCl\text{Fe} : \text{HCl} is 1:21:2.
    Moles of Fe=12×Moles of HCl\text{Fe} = \frac{1}{2} \times \text{Moles of HCl}
    Moles of Fe=12×1.5 mol=0.75 mol\text{Fe} = \frac{1}{2} \times 1.5 \text{ mol} = 0.75 \text{ mol}

  7. Calculate the mass of pure iron reacted.

    Molar mass of Fe≈56 g/mol\text{Fe} \approx 56 \text{ g/mol}
    Mass of pure Fe=Moles of Fe×Molar mass of Fe\text{Fe} = \text{Moles of Fe} \times \text{Molar mass of Fe}
    Mass of pure Fe=0.75 mol×56 g/mol=42 g\text{Fe} = 0.75 \text{ mol} \times 56 \text{ g/mol} = 42 \text{ g}

  8. Calculate the percentage purity of the iron sample.

    Total mass of impure iron sample = 5.0 g5.0 \text{ g} (This seems like a typo in the question. If 5.0g of impure iron reacted with 1.5 mol HCl, and 1.5 mol HCl reacts with 0.75 mol Fe, which is 42g of Fe, then the impure sample cannot be 5.0g. The mass of pure iron (42g) is much greater than the total impure sample (5.0g), which would lead to a purity greater than 100%, which is impossible.

    Let's re-evaluate the question. "A 5.0 g of an impure iron reacted completely with 750 cm3^3 of 2.0 mol dm−3^{-3} hydrochloric acid". This implies that the 5.0g is the total mass of the impure sample. The amount of HCl used should correspond to the pure iron in the sample.

    If the mass of pure iron is 42g, and the total impure sample is 5.0g, then the question's values are inconsistent.
    It's possible there's a typo in the volume or concentration of HCl, or the mass of the impure sample.

    Let's assume the question meant that the pure iron in the sample reacted with 750 cm3^3 of 2.0 mol dm−3^{-3} HCl, and the total impure sample was 5.0g. This would mean the mass of pure iron calculated from HCl should be less than 5.0g.

    Let's re-check the calculation for moles of HCl and mass of Fe.
    Moles of HCl = 2.0 mol/dm3×0.750 dm3=1.5 mol2.0 \text{ mol/dm}^3 \times 0.750 \text{ dm}^3 = 1.5 \text{ mol}. This is correct.
    Moles of Fe = 1.5 mol HCl×1 mol Fe2 mol HCl=0.75 mol Fe1.5 \text{ mol HCl} \times \frac{1 \text{ mol Fe}}{2 \text{ mol HCl}} = 0.75 \text{ mol Fe}. This is correct.
    Mass of Fe = 0.75 mol×56 g/mol=42 g0.75 \text{ mol} \times 56 \text{ g/mol} = 42 \text{ g}. This is correct.

    The problem statement "A 5.0 g of an impure iron reacted completely with 750 cm3^3 of 2.0 mol dm−3^{-3} hydrochloric acid" is contradictory. If 5.0g is the impure sample, then the pure iron content must be less than 5.0g. However, the calculation shows 42g of pure iron reacted. This means the amount of HCl is too high for a 5.0g impure sample.

    Given the constraint to solve the question completely and accurately using the provided numbers, I must point out the inconsistency. If I proceed with the numbers as given, the purity will be over 100%, which is chemically impossible.

    Let's assume there's a typo in the volume of HCl. What if it was 7.5 cm3^3 instead of 750 cm3^3?
    Moles of HCl = 2.0 mol/dm3×0.0075 dm3=0.015 mol2.0 \text{ mol/dm}^3 \times 0.0075 \text{ dm}^3 = 0.015 \text{ mol}.
    Moles of Fe = 0.015/2=0.0075 mol0.015 / 2 = 0.0075 \text{ mol}.
    Mass of Fe = 0.0075 mol×56 g/mol=0.42 g0.0075 \text{ mol} \times 56 \text{ g/mol} = 0.42 \text{ g}.
    Then, percentage purity = (0.42 g/5.0 g)×100%=8.4%(0.42 \text{ g} / 5.0 \text{ g}) \times 100\% = 8.4\%. This is a plausible answer.

    What if the concentration was 0.02 mol/dm3^3 instead of 2.0 mol/dm3^3?
    Moles of HCl = 0.02 mol/dm3×0.750 dm3=0.015 mol0.02 \text{ mol/dm}^3 \times 0.750 \text{ dm}^3 = 0.015 \text{ mol}.
    This leads to the same result as above.

    What if the mass of the impure sample was 50g instead of 5.0g?
    Then purity = (42 g/50 g)×100%=84%(42 \text{ g} / 50 \text{ g}) \times 100\% = 84\%. This is also plausible.

    Since I cannot assume a typo and must use the numbers given, I will state the inconsistency and calculate the purity based on the given numbers, acknowledging the impossible result.

    Mass of pure Fe\text{Fe} calculated = 42 g42 \text{ g}
    Mass of impure sample = 5.0 g5.0 \text{ g}

    Percentage purity = Mass of pure FeMass of impure sample×100%\frac{\text{Mass of pure Fe}}{\text{Mass of impure sample}} \times 100\%
    Percentage purity = 42 g5.0 g×100%\frac{42 \text{ g}}{5.0 \text{ g}} \times 100\%
    Percentage purity = 8.4×100%=840%8.4 \times 100\% = 840\%

    This result is impossible. There must be an error in the question's numerical values.
    I will state this clearly.

    Let's consider if the question implies that the 5.0g is the pure iron, and we need to find something else. No, it says "5.0 g of an impure iron".

    Let's assume the question intended for the mass of pure iron to be less than 5.0g. This means the amount of HCl given is too high.
    If I were to assume the 5.0g is the maximum possible pure iron, then the HCl amount would be less.
    But the question says "reacted completely with 750 cm3^3 of 2.0 mol dm−3^{-3} hydrochloric acid". This implies that all the reactive component (pure iron) in the 5.0g sample reacted with that specific amount of HCl.

    The only way to get a sensible answer is if one of the numbers is wrong.
    If I have to provide an answer, I must use the numbers given.
    I will state the calculation and the impossible result, and highlight the inconsistency.

    Let's re-read the question one more time to ensure no misinterpretation.
    "A 5.0 g of an impure iron reacted completely with 750 cm3^3 of 2.0 mol dm−3^{-3} hydrochloric acid to give a neutral solution. Calculate the percentage purity of the sample of iron."

    The reaction is Fe(s)+2HCl(aq)→FeCl2(aq)+H2(g)\text{Fe}(s) + 2\text{HCl}(aq) \rightarrow \text{FeCl}_2(aq) + \text{H}_2(g).
    Moles of HCl = 2.0 mol/dm3×(750/1000) dm3=1.5 mol2.0 \text{ mol/dm}^3 \times (750 / 1000) \text{ dm}^3 = 1.5 \text{ mol}.
    Moles of Fe = 1.5 mol HCl×(1 mol Fe/2 mol HCl)=0.75 mol Fe1.5 \text{ mol HCl} \times (1 \text{ mol Fe} / 2 \text{ mol HCl}) = 0.75 \text{ mol Fe}.
    Mass of Fe = 0.75 mol×56 g/mol=42 g0.75 \text{ mol} \times 56 \text{ g/mol} = 42 \text{ g}.

    This means that 42g of pure iron reacted.
    However, the total impure sample was only 5.0g.
    This is a clear contradiction. The mass of the pure component cannot be greater than the mass of the impure sample.

    I will state the steps and the result, and then explain the inconsistency.
    This is the most accurate way to handle a flawed question.

    Final check on calculations:

    1.5 mol HCl.
    1:2 ratio Fe:HCl. So 0.75 mol Fe.

    0.75 mol Fe * 56 g/mol = 42 g Fe.
    Purity = (42 g / 5.0 g) * 100% = 840%.

    This is definitely an issue with the question's numbers.
    I will proceed with the calculation and highlight the impossibility of the result.Here are the answers to question 5:

    a) (i) Hess's Law of constant heat summation states that the total enthalpy change for a chemical reaction is independent of the pathway taken, provided the initial and final conditions are the same. In other words, if a reaction can be expressed as a sum of several steps, the enthalpy change for the overall reaction is the sum of the enthalpy changes for each step.

    a) (ii) We want to calculate ΔH\Delta H for the reaction:

    C2H4(g)+H2(g)→C2H6(g)\text{C}_2\text{H}_{4(g)} + \text{H}_{2(g)} \rightarrow \text{C}_2\text{H}_{6(g)}

    Given the following reactions:

    1. C2H4(g)+3O2(g)→2CO2(g)+2H2O(l)\text{C}_2\text{H}_{4(g)} + 3\text{O}_{2(g)} \rightarrow 2\text{CO}_{2(g)} + 2\text{H}_2\text{O}_{(l)}; ΔH1=−1411 kJ mol−1\Delta H_1 = -1411 \text{ kJ mol}^{-1}
    2. C2H6(g)+72O2(g)→2CO2(g)+3H2O(l)\text{C}_2\text{H}_{6(g)} + \frac{7}{2}\text{O}_{2(g)} \rightarrow 2\text{CO}_{2(g)} + 3\text{H}_2\text{O}_{(l)}; ΔH2=−1560 kJ mol−1\Delta H_2 = -1560 \text{ kJ mol}^{-1}
    3. H2(g)+12O2(g)→H2O(l)\text{H}_{2(g)} + \frac{1}{2}\text{O}_{2(g)} \rightarrow \text{H}_2\text{O}_{(l)}; ΔH3=−1411 kJ mol−1\Delta H_3 = -1411 \text{ kJ mol}^{-1}
  9. Manipulate the given equations to match the target equation.

    • Keep reaction 1 as is, since $\text{C}_2\text
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