The combustion of one mole of benzene takes place at $298 \, K$ and $1 \, atm$. After combustion,$CO_{2(g)}$ and $H_2O_{(l)}$ are produced and $3267.0 \, kJ$ of heat is liberated. Calculate the standard enthalpy of formation,$\Delta_f H^{\ominus}$ of benzene. Standard enthalpies of formation of $CO_{2(g)}$ and $H_2O_{(l)}$ are $-393.5 \, kJ \, mol^{-1}$ and $-285.83 \, kJ \, mol^{-1}$ respectively.

Vedclass pdf generator app on play store
Vedclass iOS app on app store
(N/A) The formation reaction of benzene is given by:
$6 \, C(graphite) + 3 \, H_{2(g)} \rightarrow C_6H_{6(l)}; \Delta_f H^{\ominus} = ? \dots (i)$
The enthalpy of combustion of $1 \, mol$ of benzene is:
$C_6H_{6(l)} + \frac{15}{2} O_{2(g)}$ $\rightarrow 6 \, CO_{2(g)} + 3 \, H_2O_{(l)}; \Delta_c H^{\ominus} = -3267.0 \, kJ \, mol^{-1} \dots (ii)$
The enthalpy of formation of $1 \, mol$ of $CO_{2(g)}$ is:
$C(graphite) + O_{2(g)} \rightarrow CO_{2(g)}; \Delta_f H^{\ominus} = -393.5 \, kJ \, mol^{-1} \dots (iii)$
The enthalpy of formation of $1 \, mol$ of $H_2O_{(l)}$ is:
$H_{2(g)} + \frac{1}{2} O_{2(g)} \rightarrow H_2O_{(l)}; \Delta_f H^{\ominus} = -285.83 \, kJ \, mol^{-1} \dots (iv)$
Using Hess's Law,the enthalpy of combustion is given by:
$\Delta_c H^{\ominus} = [6 \times \Delta_f H^{\ominus}(CO_{2(g)}) + 3 \times \Delta_f H^{\ominus}(H_2O_{(l)})] - [\Delta_f H^{\ominus}(C_6H_{6(l)}) + \frac{15}{2} \Delta_f H^{\ominus}(O_{2(g)})]$
Since $\Delta_f H^{\ominus}(O_{2(g)}) = 0$,we have:
$-3267.0 = [6 \times (-393.5) + 3 \times (-285.83)] - \Delta_f H^{\ominus}(C_6H_{6(l)})$
$-3267.0 = [-2361.0 - 857.49] - \Delta_f H^{\ominus}(C_6H_{6(l)})$
$-3267.0 = -3218.49 - \Delta_f H^{\ominus}(C_6H_{6(l)})$
$\Delta_f H^{\ominus}(C_6H_{6(l)}) = -3218.49 + 3267.0 = 48.51 \, kJ \, mol^{-1}$

Explore More

Similar Questions

Calculate $\Delta S_{total}$ for the following reaction at $300 \ K$.
$NH_4NO_{3(s)} \longrightarrow NH_4^+{(aq)} + NO_3^-{(aq)}$ $(\Delta H = 28.1 \ kJ \ mol^{-1}, \Delta S_{sys} = 108.7 \ J \ K^{-1} \ mol^{-1})$

For the reaction: $A_{(g)} + B_{(s)} \rightleftharpoons 2C_{(g)} + D_{(g)}$,given $\Delta U = 5.0 \ kcal$ and $\Delta S = 50 \ cal \ K^{-1}$ at $400 \ K$. Calculate $\Delta G$ for the reaction. (in $kcal$)

Calculate the enthalpy change when $50 \ mL$ of $0.01 \ M$ $Ca(OH)_2$ reacts with $25 \ mL$ of $0.01 \ M$ $HCl$. Given that $\Delta H^o_{\text{neutralisation}}$ of strong acid and strong base is $-57.1 \ kJ \ mol^{-1}$. [Assuming that $Ca(OH)_2$ is a strong base]

Difficult
View Solution

Calculate $\Delta H^{\circ}$ for the reaction, $Na_2O_{(s)} + SO_{3(g)} \longrightarrow Na_2SO_{4(s)}$, given the following reactions:
$(A) \ Na_{(s)} + H_2O_{(l)} \longrightarrow NaOH_{(s)} + \frac{1}{2}H_{2(g)} \quad \Delta H^{\circ} = -146 \ kJ$
$(B) \ Na_2SO_{4(s)} + H_2O_{(l)} \longrightarrow 2NaOH_{(s)} + SO_{3(g)} \quad \Delta H^{\circ} = +418 \ kJ$
$(C) \ 2Na_2O_{(s)} + 2H_{2(g)} \longrightarrow 4Na_{(s)} + 2H_2O_{(l)} \quad \Delta H^{\circ} = +259 \ kJ$

Match List-$I$ with List-$II$. Given $V_1$ and $V_2$ are initial and final volumes respectively.
List-$I$ (Isothermal process) List-$II$ (Expression)
$A$. Reversible expansion $I$. $q = 0$
$B$. Free expansion $II$. $q = nRT \ln \frac{V_2}{V_1}$
$C$. Irreversible Compression $III$. $w = -P_{ext}(V_1 - V_2)$
$D$. Cyclic reversible $IV$. $\frac{q_{rev}}{T} = 0$

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo