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NEET CHEMISTRYMedium

The standard enthalpy of vaporisation ΔvapH\Delta_{vap}H^{\circ} for water at 100C100^{\circ}\text{C} is 40.66 kJ mol140.66 \text{ kJ mol}^{-1}. The internal energy of vaporisation of water at 100C100^{\circ}\text{C} (in kJ mol1\text{kJ mol}^{-1}) is: (Assume water vapour to behave like an ideal gas)

A

+37.56

B

-43.76

C

+43.76

D

+40.66

Step-by-Step Solution

For the vaporisation of water: H2O(l)H2O(g)H_2O(l) \rightarrow H_2O(g) The change in the number of moles of gaseous species, Δng=np(g)nr(g)=10=1\Delta n_g = n_{p(g)} - n_{r(g)} = 1 - 0 = 1. The relationship between enthalpy change (ΔH\Delta H) and internal energy change (ΔU\Delta U) is given by : ΔH=ΔU+ΔngRT\Delta H = \Delta U + \Delta n_g RT Rearranging the formula to find ΔU\Delta U: ΔU=ΔHΔngRT\Delta U = \Delta H - \Delta n_g RT Given data: ΔH=40.66 kJ mol1\Delta H = 40.66 \text{ kJ mol}^{-1} T=100C=373 KT = 100^{\circ}\text{C} = 373 \text{ K} R=8.314 J K1mol1=8.314×103 kJ K1mol1R = 8.314 \text{ J K}^{-1} \text{mol}^{-1} = 8.314 \times 10^{-3} \text{ kJ K}^{-1} \text{mol}^{-1} Substituting the values: ΔU=40.66 kJ mol1(1×8.314×103 kJ K1mol1×373 K)\Delta U = 40.66 \text{ kJ mol}^{-1} - (1 \times 8.314 \times 10^{-3} \text{ kJ K}^{-1} \text{mol}^{-1} \times 373 \text{ K}) ΔU=40.663.101 kJ mol1\Delta U = 40.66 - 3.101 \text{ kJ mol}^{-1} ΔU=+37.559 kJ mol1+37.56 kJ mol1\Delta U = +37.559 \text{ kJ mol}^{-1} \approx +37.56 \text{ kJ mol}^{-1}.

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