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DeltaU^(@) of combustion of CH(4(g)) at ...

`DeltaU^(@)` of combustion of `CH_(4(g))` at certain temperature is `-"393 kJ mol"^(-1)`. The value of `DeltaH^(@)` is

A

zero

B

`lt DeltaH^(@)`

C

`gt DeltaU^(@)`

D

equal to `DeltaU^(@)`

Text Solution

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The correct Answer is:
To find the value of \(\Delta H^\circ\) for the combustion of methane (\(CH_4(g)\)), we can use the relationship between \(\Delta H\) and \(\Delta U\). The equation we will use is: \[ \Delta H^\circ = \Delta U^\circ + \Delta N_g RT \] where: - \(\Delta H^\circ\) is the change in enthalpy, - \(\Delta U^\circ\) is the change in internal energy, - \(\Delta N_g\) is the change in the number of moles of gas, - \(R\) is the universal gas constant (approximately \(8.314 \, \text{J/mol·K}\)), - \(T\) is the temperature in Kelvin. ### Step 1: Write the balanced equation for the combustion of methane The balanced equation for the combustion of methane is: \[ CH_4(g) + 2 O_2(g) \rightarrow CO_2(g) + 2 H_2O(l) \] ### Step 2: Calculate \(\Delta N_g\) To find \(\Delta N_g\), we need to count the number of moles of gaseous reactants and products. - **Reactants**: - \(CH_4(g)\): 1 mole - \(O_2(g)\): 2 moles - Total = \(1 + 2 = 3\) moles of gas - **Products**: - \(CO_2(g)\): 1 mole - \(H_2O(l)\): 0 moles (liquid is not counted) - Total = \(1\) mole of gas Now, we can calculate \(\Delta N_g\): \[ \Delta N_g = \text{(moles of products)} - \text{(moles of reactants)} = 1 - 3 = -2 \] ### Step 3: Substitute values into the equation Now we can substitute the values into the equation for \(\Delta H^\circ\): Given: - \(\Delta U^\circ = -393 \, \text{kJ/mol}\) (which is \(-393,000 \, \text{J/mol}\) for consistency in units), - \(\Delta N_g = -2\), - \(R = 8.314 \, \text{J/mol·K}\), - Assume \(T\) is at standard temperature, \(T = 298 \, \text{K}\). Now substituting into the equation: \[ \Delta H^\circ = \Delta U^\circ + \Delta N_g RT \] \[ \Delta H^\circ = -393,000 \, \text{J/mol} + (-2)(8.314 \, \text{J/mol·K})(298 \, \text{K}) \] Calculating the second term: \[ \Delta H^\circ = -393,000 \, \text{J/mol} - 2 \times 8.314 \times 298 \] \[ = -393,000 \, \text{J/mol} - 4965.68 \, \text{J/mol} \] \[ = -393,000 \, \text{J/mol} - 4,965.68 \, \text{J/mol} = -397,965.68 \, \text{J/mol} \] Converting back to kJ: \[ \Delta H^\circ = -397.97 \, \text{kJ/mol} \] ### Final Answer Thus, the value of \(\Delta H^\circ\) for the combustion of methane is approximately: \[ \Delta H^\circ \approx -398 \, \text{kJ/mol} \]

To find the value of \(\Delta H^\circ\) for the combustion of methane (\(CH_4(g)\)), we can use the relationship between \(\Delta H\) and \(\Delta U\). The equation we will use is: \[ \Delta H^\circ = \Delta U^\circ + \Delta N_g RT \] where: - \(\Delta H^\circ\) is the change in enthalpy, ...
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