State and prove Hess's law of constant heat summation.

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(N/A) Hess's law states that if a reaction takes place in several steps,then its standard reaction enthalpy is the sum of the standard enthalpies of the intermediate reactions into which the overall reaction may be divided at the same temperature.
Example: Consider the formation of carbon monoxide:
$C_{(s)} + \frac{1}{2} O_{2(g)} \longrightarrow CO_{(g)} ; \Delta H^{\ominus} = ?$
Since this reaction cannot be measured directly due to the formation of $CO_2$,we use the following known reactions:
$(i) C_{(s)} + O_{2(g)} \longrightarrow CO_{2(g)} ; \Delta_{r} H^{\ominus} = -393.5 \ kJ \ mol^{-1}$
$(ii) CO_{(g)} + \frac{1}{2} O_{2(g)} \longrightarrow CO_{2(g)} ; \Delta_{r} H^{\ominus} = -283.0 \ kJ \ mol^{-1}$
To obtain the target reaction,we reverse equation $(ii)$:
$(iii) CO_{2(g)} \longrightarrow CO_{(g)} + \frac{1}{2} O_{2(g)} ; \Delta_{r} H^{\ominus} = +283.0 \ kJ \ mol^{-1}$
Adding equations $(i)$ and $(iii)$:
$C_{(s)} + \frac{1}{2} O_{2(g)}$ $\longrightarrow CO_{(g)} ; \Delta_{r} H^{\ominus} = (-393.5) + (283.0) = -110.5 \ kJ \ mol^{-1}$
In general,for a reaction $A \longrightarrow B$,if the enthalpy change is $\Delta_{r} H$ along one route and $\Delta_{r} H_1, \Delta_{r} H_2, \dots$ along another route,then $\Delta_{r} H = \sum \Delta_{r} H_i$.

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$S_{(g)} + \frac{3}{2} O_{2(g)} \rightarrow SO_{3(g)} + 2x \ kcal$
$SO_{2(g)} + \frac{1}{2} O_{2(g)} \rightarrow SO_{3(g)} + y \ kcal$
The heat of formation of $SO_{2(g)}$ is given by :

Given:
$(i) \, C(\text{graphite}) + O_{2(g)} \to CO_{2(g)}; \Delta_r H^\ominus = x \, kJ \, mol^{-1}$
$(ii) \, C(\text{graphite}) + \frac{1}{2} O_{2(g)} \to CO_{(g)}; \Delta_r H^\ominus = y \, kJ \, mol^{-1}$
$(iii) \, CO_{(g)} + \frac{1}{2} O_{2(g)} \to CO_{2(g)}; \Delta_r H^\ominus = z \, kJ \, mol^{-1}$
Based on the above thermochemical equations,find out which one of the following algebraic relationships is correct?

$C + O_2 \to CO_2; \Delta H = X$
$CO + \frac{1}{2} O_2 \to CO_2; \Delta H = Y$
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Write notes on diatomic molecules and polyatomic molecules with respect to bond dissociation enthalpy.

Calculate the heat of combustion (in $kJ$) of methane from the following data:
$(i)$ $C_{\text{(graphite)}} + 2H_{2(g)} \rightarrow CH_{4(g)} \quad \Delta H = -74.8 \ kJ$
(ii) $C_{\text{(graphite)}} + O_{2(g)} \rightarrow CO_{2(g)} \quad \Delta H = -393.5 \ kJ$
(iii) $H_{2(g)} + 1/2 O_{2(g)} \rightarrow H_2O_{(l)} \quad \Delta H = -286.2 \ kJ$

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