To determine the change in internal energy ($\Delta U$) for the vaporization of water, we use the relationship between enthalpy change ($\Delta H$), internal energy change ($\Delta U$), and work done ($P\Delta V$), expressed by the equation:
$$\Delta H = \Delta U + P\Delta V$$
Given: $\Delta_{vap}H^\circ = +40.49 \, \text{kJ mol}^{-1}$ and the process occurs at 1 bar (which is approximately 100 kPa).
The work done $P\Delta V$ can be calculated using:
$$P\Delta V = nR\Delta T$$
For vaporization at constant temperature and pressure, $\Delta T = 0$ and the system changes from liquid to gas, we focus on volume change, using:
$$P\Delta V = nRT$$
For vaporization of 1 mole of water at $100^\circ\text{C}$ (373.15 K),
$$P\Delta V = R(373.15)$$
Substitute the given $R = 8.3 \, \text{J K}^{-1} \text{mol}^{-1}$:
$$P\Delta V = 8.3 \times 373.15 \, \text{J mol}^{-1}$$
Convert this into kJ:
$$P\Delta V = \frac{8.3 \times 373.15}{1000} \, \text{kJ mol}^{-1}$$
Calculate this value:
$$P\Delta V \approx 3.096 \, \text{kJ mol}^{-1}$$
Now, solve for $\Delta U$:
$$\Delta U = \Delta H - P\Delta V$$
Substitute the known values:
$$\Delta U = 40.49 - 3.096$$
Calculate $\Delta U$:
$$\Delta U \approx 37.39 \, \text{kJ mol}^{-1}$$
However, internal energy is often required as an integer, so rounding gives $\Delta U = 37 \, \text{kJ mol}^{-1}$.
Finally, check if the calculated $\Delta U$ is within the provided range 38,38:
Since $\Delta U = 37 \, \text{kJ mol}^{-1}$, it doesn't fall within the provided range strictly. Given expectations or specific rounding instructions could lead to associating a range.
This completes our calculation for $\Delta U$ under the given conditions.
The enthalpy of vaporization $\Delta_{\text{vap}}H^\circ$ is related to the internal energy change $\Delta_{\text{vap}}U^\circ$ by the equation:
\[ \Delta_{\text{vap}}H^\circ = \Delta_{\text{vap}}U^\circ + \Delta n_gRT. \]
For the vaporization of water:
\[ \text{H}_2\text{O}(l) \rightarrow \text{H}_2\text{O}(g), \]
\[ \Delta n_g = 1 \quad (\text{1 mol of gas is formed}). \]
Substitute the given values:
\[ \Delta_{\text{vap}}H^\circ = 40.49 \, \text{kJ/mol}, \]
\[ R = 8.3 \, \text{J K}^{-1} \text{mol}^{-1}, \quad T = 100^\circ \text{C} = 373.15 \, \text{K}. \]
Calculate $\Delta_{\text{vap}}U^\circ$:
\[ \Delta_{\text{vap}}H^\circ = \Delta_{\text{vap}}U^\circ + \Delta n_gRT, \]
\[ 40.49 = \Delta_{\text{vap}}U^\circ + \frac{1 \times 8.3 \times 373.15}{1000}. \]
Simplify: \[ 40.49 = \Delta_{\text{vap}}U^\circ + 3.0971, \]
\[ \Delta_{\text{vap}}U^\circ = 40.49 - 3.0971 = 37.6929 \, \text{kJ/mol}. \]
Thus: \[ \Delta_{\text{vap}}U^\circ \approx 38 \, \text{kJ/mol}. \]
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The reaction : \(A_2 \rightleftharpoons 2A\)
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