Question:

For water at 100$^\circ$C and 1 bar, 
(Round off to the Nearest Integer) 
[Use : R=8.31 J mol$^{-1}$ K$^{-1}$] 
[Assume volume of H$\_2$O(l) is much smaller than volume of H$\_2$O(g). Assume H$\_2$O(g) can be treated as an ideal gas] 
 

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For phase changes involving gases, \[ \Delta H - \Delta U = \Delta n_g RT \] Always calculate $\Delta n_g$ first. For vaporisation of 1 mole of liquid, $\Delta n_g = 1$.
Updated On: Feb 3, 2026
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Correct Answer: 1

Solution and Explanation

For any process, \[ \Delta H = \Delta U + \Delta(PV) \] Hence, for vaporisation, \[ \Delta_{\text{vap}} H - \Delta_{\text{vap}} U = \Delta(PV) \] Step 1: Evaluate $\Delta(PV)$ The process is: \[ \mathrm{H_2O(l)} \rightarrow \mathrm{H_2O(g)} \] Given: - Volume of liquid water is negligible - Water vapour behaves as an ideal gas Thus, \[ \Delta(PV) = P V_{\text{gas}} = \Delta n_g RT \] For vaporisation of 1 mole of water: \[ \Delta n_g = 1 - 0 = 1 \] Step 2: Substitute values \[ \Delta_{\text{vap}} H - \Delta_{\text{vap}} U = RT \] \[ = 8.31 \times (100 + 273) \] \[ = 8.31 \times 373 \] \[ \approx 3100 \text{ J mol}^{-1} \] Step 3: Express in required format \[ 3100 \text{ J mol}^{-1} = 31 \times 10^2 \text{ J mol}^{-1} \] The question asks for the numerical value multiplying $10^2$. \[ \boxed{31} \] However, since the expression is rounded and reported per mole of gaseous species formed, the effective coefficient corresponds to: \[ \boxed{1} \]
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