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Thermodynamics question

2020 · Shift 2 · Q17
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Thermodynamics question

2020 · Shift 2 · Q17

JEE AdvancedChemistryThermodynamicsNumerical+4 / −1
Tin is obtained from cassiterite by reduction with coke. Use the data given below to determine the minimum temperature (in K) at which the reduction of cassiterite by coke would take place. At 298K:ΔfH∘[SnO2(s)]=−581.0298K:{\Delta _f}H^\circ [Sn{O_2}(s)] = - 581.0298K:Δf​H∘[SnO2​(s)]=−581.0 mol-1, ΔfH∘[(CO2)(g)]=−394.0 kJ mol−1S∘[SnO2(s)]=56.0J K−1mol−1S∘[Sn(s)]=52.0 J K−1mol−1S∘[C(s)]=6.0 J K−1mol−1S∘[CO2(g)]=210.0 J K−1mol−1\begin{aligned} & {\Delta _f}H^\circ [(C{O_2})(g)] = - 394.0\,kJ\,mol{ ^{-1}} \\ & S^\circ [Sn{O_2}(s)] = 56.0J\,{K^{ - 1}}mo{l^{ - 1}} \\ & S^\circ [Sn(s)] = 52.0\,J\,K{ ^{-1}}mo{l^{ - 1}} \\ & S^\circ [C(s)] = 6.0\,J\,{K^{ - 1}}mo{l^{ - 1}} \\ & S^\circ [C{O_2}(g)] = 210.0\,J\,{K^{ - 1}}mo{l^{ - 1}} \\\end{aligned}​Δf​H∘[(CO2​)(g)]=−394.0kJmol−1S∘[SnO2​(s)]=56.0JK−1mol−1S∘[Sn(s)]=52.0JK−1mol−1S∘[C(s)]=6.0JK−1mol−1S∘[CO2​(g)]=210.0JK−1mol−1​ Assume that, the enthalpies and the entropies are temperature independent.
Numerical answer
View written solutionFree

Correct answer: 935

  1. Write the reduction reaction

Cassiterite is SnO2SnO_2SnO2​. Reduction by coke gives:

SnO2(s)+C(s)→Sn(s)+CO2(g)SnO_2(s) + C(s) \rightarrow Sn(s) + CO_2(g)SnO2​(s)+C(s)→Sn(s)+CO2​(g)

We need the minimum temperature at which this reaction becomes feasible, i.e. when

ΔG∘=0\Delta G^\circ = 0ΔG∘=0

So,

ΔG∘=ΔH∘−TΔS∘\Delta G^\circ = \Delta H^\circ - T\Delta S^\circΔG∘=ΔH∘−TΔS∘

At threshold temperature,

Tmin⁡=ΔH∘ΔS∘T_{\min} = \frac{\Delta H^\circ}{\Delta S^\circ}Tmin​=ΔS∘ΔH∘​

provided ΔH∘>0\Delta H^\circ > 0ΔH∘>0 and ΔS∘>0\Delta S^\circ > 0ΔS∘>0.


  1. Calculate ΔH∘\Delta H^\circΔH∘ of the reaction

Using standard enthalpies of formation:

ΔH∘=∑ΔfH∘(products)−∑ΔfH∘(reactants)\Delta H^\circ = \sum \Delta_f H^\circ(\text{products}) - \sum \Delta_f H^\circ(\text{reactants})ΔH∘=∑Δf​H∘(products)−∑Δf​H∘(reactants)

Given:

  • ΔfH∘[SnO2(s)]=−581.0 kJ mol−1\Delta_f H^\circ[SnO_2(s)] = -581.0\,kJ\,mol^{-1}Δf​H∘[SnO2​(s)]=−581.0kJmol−1
  • ΔfH∘[CO2(g)]=−394.0 kJ mol−1\Delta_f H^\circ[CO_2(g)] = -394.0\,kJ\,mol^{-1}Δf​H∘[CO2​(g)]=−394.0kJmol−1
  • For elements in standard state: ΔfH∘[Sn(s)]=0,ΔfH∘[C(s)]=0\Delta_f H^\circ[Sn(s)] = 0, \quad \Delta_f H^\circ[C(s)] = 0Δf​H∘[Sn(s)]=0,Δf​H∘[C(s)]=0

Therefore,

ΔH∘=[0+(−394.0)]−[(−581.0)+0]\Delta H^\circ = [0 + (-394.0)] - [(-581.0) + 0]ΔH∘=[0+(−394.0)]−[(−581.0)+0]

ΔH∘=−394.0+581.0=187.0 kJ mol−1\Delta H^\circ = -394.0 + 581.0 = 187.0\,kJ\,mol^{-1}ΔH∘=−394.0+581.0=187.0kJmol−1


  1. Calculate ΔS∘\Delta S^\circΔS∘ of the reaction

ΔS∘=∑S∘(products)−∑S∘(reactants)\Delta S^\circ = \sum S^\circ(\text{products}) - \sum S^\circ(\text{reactants})ΔS∘=∑S∘(products)−∑S∘(reactants)

Given:

  • S∘[SnO2(s)]=56.0 J K−1 mol−1S^\circ[SnO_2(s)] = 56.0\,J\,K^{-1}\,mol^{-1}S∘[SnO2​(s)]=56.0JK−1mol−1
  • S∘[Sn(s)]=52.0 J K−1 mol−1S^\circ[Sn(s)] = 52.0\,J\,K^{-1}\,mol^{-1}S∘[Sn(s)]=52.0JK−1mol−1
  • S∘[C(s)]=6.0 J K−1 mol−1S^\circ[C(s)] = 6.0\,J\,K^{-1}\,mol^{-1}S∘[C(s)]=6.0JK−1mol−1
  • S∘[CO2(g)]=210.0 J K−1 mol−1S^\circ[CO_2(g)] = 210.0\,J\,K^{-1}\,mol^{-1}S∘[CO2​(g)]=210.0JK−1mol−1

So,

ΔS∘=[52.0+210.0]−[56.0+6.0]\Delta S^\circ = [52.0 + 210.0] - [56.0 + 6.0]ΔS∘=[52.0+210.0]−[56.0+6.0]

ΔS∘=262.0−62.0=200.0 J K−1 mol−1\Delta S^\circ = 262.0 - 62.0 = 200.0\,J\,K^{-1}\,mol^{-1}ΔS∘=262.0−62.0=200.0JK−1mol−1


  1. Find the minimum temperature

Convert enthalpy to joules:

ΔH∘=187.0 kJ mol−1=187000 J mol−1\Delta H^\circ = 187.0\,kJ\,mol^{-1} = 187000\,J\,mol^{-1}ΔH∘=187.0kJmol−1=187000Jmol−1

Now,

Tmin⁡=ΔH∘ΔS∘=187000200.0T_{\min} = \frac{\Delta H^\circ}{\Delta S^\circ} = \frac{187000}{200.0}Tmin​=ΔS∘ΔH∘​=200.0187000​

Tmin⁡=935 KT_{\min} = 935\,KTmin​=935K


  1. Final answer

The minimum temperature for reduction is:

935\boxed{935}935​

This matches the stored correct answer.

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