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Thermodynamics question

2006 · Shift 0 · Q4
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Thermodynamics question

2006 · Shift 0 · Q4

JEE MainChemistryThermodynamicsMCQ+4 / −1
The enthalpy changes for the following processes are listed below : Cl2Cl_2Cl2​(g) = 2ClClCl(g), 242.3 kJ mol–1 I2I_2I2​(g) = 2III(g), 151.0 kJ mol–1 IClIClICl(g) = III(g) + ClClCl(g), 211.3 kJ mol–1 I2I_2I2​(s) = I2I_2I2​(g), 62.76 kJ mol–1 Given that the standard states for iodine and chlorine are I2I_2I2​(s) and Cl2Cl_2Cl2​(g), the standard enthalpy of formation for IClIClICl(g) is :
  1. A
    –14.6 kJ mol–1
  2. B
    –16.8 kJ mol–1
  3. C
    +16.8 kJ mol–1
  4. D
    +244.8 kJ mol–1
View written solutionFree

Correct answer: C

  1. Write the required formation reaction

The standard enthalpy of formation of ICl(g)ICl(g)ICl(g) is for:

12I2(s)+12Cl2(g)→ICl(g)\frac{1}{2}I_2(s) + \frac{1}{2}Cl_2(g) \rightarrow ICl(g)21​I2​(s)+21​Cl2​(g)→ICl(g)

We need ΔHf∘\Delta H_f^\circΔHf∘​ for this reaction.


  1. Use the given bond dissociation / phase-change data

Given:

Cl2(g)→2Cl(g),ΔH=242.3 kJ mol−1Cl_2(g) \rightarrow 2Cl(g), \quad \Delta H = 242.3\,\text{kJ mol}^{-1}Cl2​(g)→2Cl(g),ΔH=242.3kJ mol−1 I2(g)→2I(g),ΔH=151.0 kJ mol−1I_2(g) \rightarrow 2I(g), \quad \Delta H = 151.0\,\text{kJ mol}^{-1}I2​(g)→2I(g),ΔH=151.0kJ mol−1 ICl(g)→I(g)+Cl(g),ΔH=211.3 kJ mol−1ICl(g) \rightarrow I(g)+Cl(g), \quad \Delta H = 211.3\,\text{kJ mol}^{-1}ICl(g)→I(g)+Cl(g),ΔH=211.3kJ mol−1 I2(s)→I2(g),ΔH=62.76 kJ mol−1I_2(s) \rightarrow I_2(g), \quad \Delta H = 62.76\,\text{kJ mol}^{-1}I2​(s)→I2​(g),ΔH=62.76kJ mol−1


  1. Convert reactants in standard states into atoms

From 12I2(s)\frac12 I_2(s)21​I2​(s) to I(g)I(g)I(g):

  • Sublimation of iodine: 12I2(s)→12I2(g),ΔH=62.762=31.38\frac12 I_2(s) \rightarrow \frac12 I_2(g), \quad \Delta H = \frac{62.76}{2}=31.3821​I2​(s)→21​I2​(g),ΔH=262.76​=31.38

  • Dissociation of gaseous iodine: 12I2(g)→I(g),ΔH=151.02=75.5\frac12 I_2(g) \rightarrow I(g), \quad \Delta H = \frac{151.0}{2}=75.521​I2​(g)→I(g),ΔH=2151.0​=75.5

So,

12I2(s)→I(g),ΔH=31.38+75.5=106.88 kJ mol−1\frac12 I_2(s) \rightarrow I(g), \quad \Delta H = 31.38+75.5=106.88\,\text{kJ mol}^{-1}21​I2​(s)→I(g),ΔH=31.38+75.5=106.88kJ mol−1

From 12Cl2(g)\frac12 Cl_2(g)21​Cl2​(g) to Cl(g)Cl(g)Cl(g):

12Cl2(g)→Cl(g),ΔH=242.32=121.15 kJ mol−1\frac12 Cl_2(g) \rightarrow Cl(g), \quad \Delta H = \frac{242.3}{2}=121.15\,\text{kJ mol}^{-1}21​Cl2​(g)→Cl(g),ΔH=2242.3​=121.15kJ mol−1

Thus,

12I2(s)+12Cl2(g)→I(g)+Cl(g)\frac12 I_2(s)+\frac12 Cl_2(g) \rightarrow I(g)+Cl(g)21​I2​(s)+21​Cl2​(g)→I(g)+Cl(g)

has

ΔH=106.88+121.15=228.03 kJ mol−1\Delta H = 106.88+121.15=228.03\,\text{kJ mol}^{-1}ΔH=106.88+121.15=228.03kJ mol−1


  1. Form ICl(g)ICl(g)ICl(g) from atoms

Given dissociation:

ICl(g)→I(g)+Cl(g),ΔH=211.3 kJ mol−1ICl(g) \rightarrow I(g)+Cl(g), \quad \Delta H = 211.3\,\text{kJ mol}^{-1}ICl(g)→I(g)+Cl(g),ΔH=211.3kJ mol−1

So the reverse reaction is:

I(g)+Cl(g)→ICl(g),ΔH=−211.3 kJ mol−1I(g)+Cl(g) \rightarrow ICl(g), \quad \Delta H = -211.3\,\text{kJ mol}^{-1}I(g)+Cl(g)→ICl(g),ΔH=−211.3kJ mol−1


  1. Apply Hess's law

Add the two steps:

12I2(s)+12Cl2(g)→I(g)+Cl(g)(228.03)\frac12 I_2(s)+\frac12 Cl_2(g) \rightarrow I(g)+Cl(g) \quad (228.03)21​I2​(s)+21​Cl2​(g)→I(g)+Cl(g)(228.03) I(g)+Cl(g)→ICl(g)(−211.3)I(g)+Cl(g) \rightarrow ICl(g) \quad (-211.3)I(g)+Cl(g)→ICl(g)(−211.3)

Net:

12I2(s)+12Cl2(g)→ICl(g)\frac12 I_2(s)+\frac12 Cl_2(g) \rightarrow ICl(g)21​I2​(s)+21​Cl2​(g)→ICl(g)

Therefore,

ΔHf∘=228.03−211.3=16.73 kJ mol−1\Delta H_f^\circ = 228.03-211.3=16.73\,\text{kJ mol}^{-1}ΔHf∘​=228.03−211.3=16.73kJ mol−1

So,

ΔHf∘(ICl(g))≈+16.8 kJ mol−1\boxed{\Delta H_f^\circ\big(ICl(g)\big) \approx +16.8\,\text{kJ mol}^{-1}}ΔHf∘​(ICl(g))≈+16.8kJ mol−1​


  1. Check options
  • A: −14.6-14.6−14.6 ❌
  • B: −16.8-16.8−16.8 ❌
  • C: +16.8+16.8+16.8 ✅
  • D: +244.8+244.8+244.8 ❌

Hence the correct option is C.

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