The enthalpies of combustion of carbon and carbon monoxide are $-393.5 \, kJ$ and $-283 \, kJ$ respectively. Calculate the enthalpy of formation of carbon monoxide in $kJ$. (in $.5$)

Calculate the enthalpy change in $kJ$ for the reaction: $2C_{(graphite)} + 2H_{2(g)} \to C_2H_{4(g)}$
$C_{(graphite)} + O_{2(g)} \to CO_{2(g)} \quad \Delta H = -393.5 \ kJ$
$C_2H_{4(g)} + 3O_{2(g)} \to 2CO_{2(g)} + 2H_2O_{(l)} \quad \Delta H = -1410.9 \ kJ$
$H_{2(g)} + 1/2O_{2(g)} \to H_2O_{(l)} \quad \Delta H = -285.8 \ kJ$

Assertion $(A)$: Formation of $H_2O_{(\ell)}$ from $H_{2(g)}$ and $O_{2(g)}$ is more exothermic than formation of $H_2O_{(g)}$ from $H_{2(g)}$ and $O_{2(g)}$.
Reason $(R)$: $H_2O_{(\ell)}$ has more attraction force than $H_2O_{(g)}$ and it is more stable than $H_2O_{(g)}$.

Calculate the enthalpy change of vaporisation of benzene if $13 \ g$ of benzene vaporised by supplying $5.1 \ kJ$ of heat.

The values of heat of formation of $SO_2$ and $SO_3$ are $-298.2 \ kJ$ and $-395.2 \ kJ$ respectively. The heat of reaction for the following reaction will be $... \ kJ$
$SO_2 + \frac{1}{2}O_2 \to SO_3$

Given the thermochemical equation,$2 H_{2(g)} + O_{2(g)} \rightarrow 2 H_2O_{(l)}$; $\Delta H = -571.6 \ kJ$. The heat of decomposition of water is: