Calculate the enthalpy of formation of carbon monoxide $(CO).$ Given: $C_{(s)} + O_{2(g)} \rightarrow CO_{2(g)}, \Delta H = -393.3 \ kJ \ mol^{-1}$ and $CO_{(g)} + \frac{1}{2} O_{2(g)} \rightarrow CO_{2(g)}, \Delta H = -282.2 \ kJ \ mol^{-1}.$

  • A
    $-111.1 \ kJ \ mol^{-1}$
  • B
    $676.1 \ kJ \ mol^{-1}$
  • C
    $-282.8 \ kJ \ mol^{-1}$
  • D
    $300.0 \ kJ \ mol^{-1}$

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From the following bond energies:
$H-H$ bond energy$431.37 \text{ kJ mol}^{-1}$
$C=C$ bond energy$606.10 \text{ kJ mol}^{-1}$
$C-C$ bond energy$336.49 \text{ kJ mol}^{-1}$
$C-H$ bond energy$410.50 \text{ kJ mol}^{-1}$

Enthalpy for the reaction $CH_2=CH_2 + H-H \to CH_3-CH_3$ will be .............. $\text{kJ mol}^{-1}$

The enthalpy of combustion of benzene from the following data will be
$(i) \ 6C_{(s)} + 3H_{2(g)} \to C_6H_{6(l)} ; \Delta H = +45.9 \ kJ$
$(ii) \ H_{2(g)} + \frac{1}{2}O_{2(g)} \to H_2O_{(l)} ; \Delta H = -285.9 \ kJ$
$(iii) \ C_{(s)} + O_{2(g)} \to CO_{2(g)} ; \Delta H = -393.5 \ kJ$
.....$kJ$

The bond dissociation energies of $X_2$,$Y_2$ and $XY$ are in the ratio of $1 : 0.5 : 1$. $\Delta H$ for the formation of $XY$ is $-200 \ kJ \ mol^{-1}$. The bond dissociation energy of $X_2$ will be $...... \ kJ \ mol^{-1}$.

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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The heats of combustion of rhombic and monoclinic sulphur are respectively $70960 \ cal$ and $71030 \ cal$. What will be the heat of conversion of rhombic sulphur to monoclinic? $(cal)$

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