$S_{\text{(rhombic)}} + O_{2(g)} \rightarrow SO_{2(g)}; \Delta H = -297.5 \, kJ$
$S_{\text{(monoclinic)}} + O_{2(g)} \rightarrow SO_{2(g)}; \Delta H = -300 \, kJ$
From the given data,which of the following statements is correct?

  • A
    $S_{\text{(rhombic)}}$ is more stable than $S_{\text{(monoclinic)}}$.
  • B
    $S_{\text{(monoclinic)}}$ is more stable than $S_{\text{(rhombic)}}$.
  • C
    The transition of $S_{\text{(rhombic)}}$ to $S_{\text{(monoclinic)}}$ is exothermic.
  • D
    The transition of $S_{\text{(monoclinic)}}$ to $S_{\text{(rhombic)}}$ is endothermic.

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The enthalpy changes for the following processes are listed below:
$Cl_{2(g)} \rightarrow 2Cl_{(g)}$$242.3 \ kJ \ mol^{-1}$
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$ICl_{(g)} \rightarrow I_{(g)} + Cl_{(g)}$$211.3 \ kJ \ mol^{-1}$
$I_{2(s)} \rightarrow I_{2(g)}$$62.76 \ kJ \ mol^{-1}$

Given that the standard states for iodine and chlorine are $I_{2(s)}$ and $Cl_{2(g)}$,the standard enthalpy of formation for $ICl_{(g)}$ is : ............... $kJ \ mol^{-1}$

The $\Delta H_f^o$ 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 (in $kJ$) for the reaction $CO_{2(g)} + H_{2(g)} \to CO_{(g)} + H_2O_{(g)}$ is

The standard enthalpy of atomization of ethane according to the equation $C_2H_{6(g)} \rightarrow 2C_{(g)} + 6H_{(g)}$ is $622 \ kJ \ mol^{-1}$. If the standard mean $C-H$ bond dissociation enthalpy is $90 \ kJ \ mol^{-1}$,the standard mean dissociation enthalpy of the $C-C$ bond (in $kJ \ mol^{-1}$) is:

$C + \frac{1}{2} O_2 \to CO; \Delta H = -42 \ kJ$
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