Skip to content
Exercises · 5.15

Q.Calculate the enthalpy change for the process CCl4(g)→C(g)+4Cl(g)CCl_4(g) \rightarrow C(g) + 4Cl(g) and calculate the bond enthalpy of C–Cl in CCl4(g)CCl_4(g). ΔvapH(CCl4)=30.5\Delta_{vap}H(CCl_4) = 30.5 kJ mol−1^{-1}; ΔfH(CCl4)=−135.5\Delta_f H(CCl_4) = -135.5 kJ mol−1^{-1}; ΔaH(C)=715.0\Delta_a H(C) = 715.0 kJ mol−1^{-1} (enthalpy of atomisation); ΔaH(Cl2)=242\Delta_a H(Cl_2) = 242 kJ mol−1^{-1}.

Punjab PsebTextbookSubjective· 3mImportance★★★★★est
30% · 29/98 Questions
🔒 Locked · start free trial →

You're viewing a preview — the full solution, concept, methods & PYQ mapping are locked.

Start your 14-day free trial to unlock the full solution →

To break CCl4(g)CCl_4(g) into gaseous atoms, we reverse its formation and add atomisation energies for the elements. The total enthalpy change is 13041304 kJ mol−1^{-1}, giving a C–Cl bond enthalpy of 326326 kJ mol−1^{-1}.

Why this approach works

Bond enthalpy measures the energy needed to break one mole of a particular bond in the gas phase, producing gaseous atoms. For CCl4CCl_4, we have four C–Cl bonds, so the process CCl4(g)→C(g)+4Cl(g)CCl_4(g) \rightarrow C(g) + 4Cl(g) requires breaking all four. The challenge is that we're not given this dissociation energy directly—instead, we have formation data and atomisation energies.

The key insight: we can construct any thermochemical process by combining others through Hess's Law. We'll build a cycle that takes CCl4(g)CCl_4(g) back to its elements in their standard states, then atomises those elements into gaseous atoms.

Step-by-step construction

1. Reverse the formation of CCl4(l)CCl_4(l)

The standard enthalpy of formation tells us:

C(s)+2Cl2(g)→CCl4(l)ΔH=−135.5 kJ mol−1C(s) + 2Cl_2(g) \rightarrow CCl_4(l) \quad \Delta H = -135.5 \text{ kJ mol}^{-1}

Reversing this:

CCl4(l)→C(s)+2Cl2(g)ΔH=+135.5 kJ mol−1CCl_4(l) \rightarrow C(s) + 2Cl_2(g) \quad \Delta H = +135.5 \text{ kJ mol}^{-1}

2. Vaporise CCl4CCl_4 to get the gaseous molecule

We need CCl4(g)CCl_4(g), not the liquid. The vaporisation enthalpy is given:

CCl4(l)→CCl4(g)ΔH=+30.5 kJ mol−1CCl_4(l) \rightarrow CCl_4(g) \quad \Delta H = +30.5 \text{ kJ mol}^{-1}

Combining steps 1 and 2, we can write:

CCl4(g)→C(s)+2Cl2(g)ΔH=+135.5−30.5=+105.0 kJ mol−1CCl_4(g) \rightarrow C(s) + 2Cl_2(g) \quad \Delta H = +135.5 - 30.5 = +105.0 \text{ kJ mol}^{-1}

Watch out

A common mistake is forgetting to account for the phase of CCl4CCl_4. The formation enthalpy given is for the liquid, so we must subtract the vaporisation energy to work with the gas.

3. Atomise carbon

Now we break the solid carbon into gaseous atoms:

C(s)→C(g)ΔH=+715.0 kJ mol−1C(s) \rightarrow C(g) \quad \Delta H = +715.0 \text{ kJ mol}^{-1}

This is the enthalpy of atomisation (or sublimation energy) of carbon.

4. Atomise chlorine

We need four moles of Cl(g)Cl(g), which means breaking two moles of Cl2Cl_2 bonds:

2Cl2(g)→4Cl(g)ΔH=2×242=+484 kJ mol−12Cl_2(g) \rightarrow 4Cl(g) \quad \Delta H = 2 \times 242 = +484 \text{ kJ mol}^{-1}

Each Cl2Cl_2 molecule requires 242242 kJ mol−1^{-1} to dissociate.

5. Sum the entire cycle …

Unlock everything free for 14 days

  • Full step-by-step solutions
  • Concept-first explanations
  • Methods, shortcuts & mistakes
  • PYQ mapping + timed mock tests

Full access for 14 days. No credit card required.