$C_{(graphite)} + O_{2(g)} \to CO_{2(g)}; \Delta H = - 94.05 \ k \ cal \ mol^{-1}$
$C_{(diamond)} + O_{2(g)} \to CO_{2(g)}; \Delta H = - 94.50 \ k \ cal \ mol^{-1}$
Therefore:

For the reaction $2 Cl ( g ) \rightarrow Cl _{2}( g )$,the correct option is

$A$ solution of $500 \ mL$ of $0.2 \ M \ KOH$ and $500 \ mL$ of $0.2 \ M \ HCl$ is mixed and stirred; the rise in temperature is $T_1$. The experiment is repeated using $250 \ mL$ each of solution,the temperature raised is $T_2$. Which of the following is true?

Products are favoured in a chemical reaction taking place at a constant temperature and pressure. Consider the following statements: $(i)$ The change in Gibbs energy for the reaction is negative. $(ii)$ The total change in Gibbs energy for the reaction and the surroundings is negative. $(iii)$ The change in entropy for the reaction is positive. $(iv)$ The total change in entropy for the reaction and the surroundings is positive. The statements which are always true are:

The entropy versus temperature plot for phases $\alpha$ and $\beta$ at $1 \ bar$ pressure is given. $S_T$ and $S_0$ are entropies of the phases at temperatures $T$ and $0 \ K$,respectively.
The transition temperature for $\alpha$ to $\beta$ phase change is $600 \ K$ and $C_{p, \beta} - C_{p, \alpha} = 1 \ J \ mol^{-1} \ K^{-1}$. Assume $(C_{p, \beta} - C_{p, \alpha})$ is independent of temperature in the range of $200$ to $700 \ K$. $C_{p, \alpha}$ and $C_{p, \beta}$ are heat capacities of $\alpha$ and $\beta$ phases,respectively.
$(1)$ The value of entropy change,$S_{\beta} - S_{\alpha}$ (in $J \ mol^{-1} \ K^{-1}$),at $300 \ K$ is. . . . . . .
$(2)$ The value of enthalpy change,$H_{\beta} - H_{\alpha}$ (in $J \ mol^{-1}$),at $300 \ K$ is.
[Use : $\ln 2 = 0.69$,Given : $S_{\beta} - S_{\alpha} = 0$ at $0 \ K$]

Calculate the work done in $kJ$ when $3$ moles of an ideal gas at $27^{\circ} C$ expand isothermally and reversibly from $10 \ atm$ to $1 \ atm$ $[R=8.314 \ J \ K^{-1} \ mol^{-1}]$