When it is not possible to calculate the enthalpy of a reaction experimentally,it can be calculated by .....

  • A
    Kirchhoff's equation
  • B
    Hess's law
  • C
    Henry's law
  • D
    Clapeyron equation

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Similar Questions

If $S + O_2 \to SO_2; (\Delta H = -298.2 \ kJ)$,$SO_2 + \frac{1}{2} O_2 \to SO_3; (\Delta H = -98.2 \ kJ)$,$SO_3 + H_2O \to H_2SO_4; (\Delta H = -130.2 \ kJ)$,$H_2 + \frac{1}{2} O_2 \to H_2O; (\Delta H = -287.3 \ kJ)$,then the enthalpy of formation of $H_2SO_4$ at $298 \ K$ will be......$kJ$.

Which of the following substances has the highest value of standard molar enthalpy of formation at $298 \ K$?

From the following data,the heat of transition for the conversion of rhombic sulfur $(S_R)$ to monoclinic sulfur $(S_M)$ in $kJ$ is:
$S_R + O_{2(g)} \to SO_{2(g)}; \Delta H = -296.90 \ kJ$
$S_M + O_{2(g)} \to SO_{2(g)}; \Delta H = -299.40 \ kJ$

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The bond dissociation enthalpies of $H_2, Cl_2$ and $HCl$ are $434, 242$ and $431 \, kJ/mol$ respectively. The enthalpy of formation of $HCl$ is ..... $kJ/mol$.

$XeF_{2(g)} + H_{2(g)} \to 2HF_{(g)} + Xe_{(g)}$,$\Delta H^o = -430 \ kJ$
Bond energy:
$H-H = 435 \ kJ/mol$
$H-F = 565 \ kJ/mol$
Calculate the average bond energy of the $Xe-F$ bond in $kJ/mol$.

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