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Problems · Problem 5.9

Q.The combustion of one mole of benzene takes place at 298 K and 1 atm. After combustion, CO2(g)CO_2(g) and H2O(l)H_2O(l) are produced and 3267.0 kJ of heat is liberated. Calculate the standard enthalpy of formation, ΔfH⊖\Delta_f H^\ominus of benzene. Standard enthalpies of formation of CO2(g)CO_2(g) and H2O(l)H_2O(l) are –393.5 kJ mol−1^{-1} and –285.83 kJ mol−1^{-1} respectively.

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Apply Hess's law: ΔcH⊖=∑ΔfH⊖(products)−ΔfH⊖(benzene)\Delta_c H^\ominus = \sum \Delta_f H^\ominus(\text{products}) - \Delta_f H^\ominus(\text{benzene}). Solving with the given data gives ΔfH⊖(C6H6)=+48.51 kJ mol−1\Delta_f H^\ominus(\text{C}_6\text{H}_6) = +48.51\ \text{kJ mol}^{-1}.

The combustion reaction

C6H6(l)+152 O2(g)→6 CO2(g)+3 H2O(l),ΔcH⊖=−3267.0 kJ mol−1.\text{C}_6\text{H}_6(l) + \tfrac{15}{2}\,\text{O}_2(g) \rightarrow 6\,\text{CO}_2(g) + 3\,\text{H}_2\text{O}(l),\qquad \Delta_c H^\ominus = -3267.0\ \text{kJ mol}^{-1}.

The heat liberated (3267.0 kJ3267.0\ \text{kJ}) is exothermic, hence the negative sign.

Hess's-law relation

ΔcH⊖=[6 ΔfH⊖(CO2)+3 ΔfH⊖(H2O)]−ΔfH⊖(C6H6),\Delta_c H^\ominus = \big[6\,\Delta_f H^\ominus(\text{CO}_2) + 3\,\Delta_f H^\ominus(\text{H}_2\text{O})\big] - \Delta_f H^\ominus(\text{C}_6\text{H}_6),

with ΔfH⊖(O2)=0\Delta_f H^\ominus(\text{O}_2) = 0 (element in its standard state).

Substitute the data

6 ΔfH⊖(CO2)=6×(−393.5)=−2361.0 kJ,6\,\Delta_f H^\ominus(\text{CO}_2) = 6 \times (-393.5) = -2361.0\ \text{kJ},

3 ΔfH⊖(H2O)=3×(−285.83)=−857.49 kJ,3\,\Delta_f H^\ominus(\text{H}_2\text{O}) = 3 \times (-285.83) = -857.49\ \text{kJ},

sum over products=−2361.0+(−857.49)=−3218.49 kJ.\text{sum over products} = -2361.0 + (-857.49) = -3218.49\ \text{kJ}.

So …

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