The $\Delta H_f$ for $CO_{2(g)}$,$CO_{(g)}$ and $H_2O_{(g)}$ are $-393.5$,$-110.5$ and $-241.8 \ kJ \ mol^{-1}$ respectively. The standard enthalpy change for the reaction is:
$CO_{2(g)} + H_{2(g)} \to CO_{(g)} + H_2O_{(g)}$

  • A
    $524.1 \ kJ \ mol^{-1}$
  • B
    $41.2 \ kJ \ mol^{-1}$
  • C
    $-262.5 \ kJ \ mol^{-1}$
  • D
    $-41.2 \ kJ \ mol^{-1}$

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From the given data at $298 \, K$:
$\Delta H_f^o [CO_2, g] = -394 \, kJ/mol$
$\Delta H_f^o [H_2O, l] = -286 \, kJ/mol$
$\Delta H_f^o [propene, g] = 20 \, kJ/mol$
$cyclopropane (g) \to propene (g)$; $\Delta H^o_{isomerisation} = -33 \, kJ/mol$.
Calculate $\Delta H^o_{combustion} [cyclopropane, g]$.
$...... \, kJ/mol$

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Which of the following pairs has a heat of neutralisation equal to $13.7 \, Kcal$?

At $25^{\circ} \text{C}$, the standard enthalpies of combustion of $H_2(g)$, cyclohexene $(C_6H_{10})$, and cyclohexane $(C_6H_{12})$ are $-241 \text{ kJ mol}^{-1}$, $-3800 \text{ kJ mol}^{-1}$, and $-3920 \text{ kJ mol}^{-1}$ respectively. Calculate the heat of hydrogenation of cyclohexene.

$Fe_2O_{3(s)} + \frac{3}{2} C_{(s)} \to \frac{3}{2} CO_{2(g)} + 2Fe_{(s)}$
$\Delta H^o = +234.1 \ kJ$
$C_{(s)} + O_{2(g)} \to CO_{2(g)}$
$\Delta H^o = -393.5 \ kJ$
Use these equations and $\Delta H^o$ values to calculate $\Delta H^o$ for this reaction:
$4Fe_{(s)} + 3O_{2(g)} \to 2Fe_2O_{3(s)}$
..... $kJ$

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Hess's law is based on

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