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At low pressure, the Vander Waal’s equat...

At low pressure, the Vander Waal’s equation is reduced to

A

`Z=(PV_(m))/(RT)=1-(aP)/(RT)`

B

`Z=(PV_(m))/(RT)=1+(bP)/(RT)`

C

`PV_(m)=RT`

D

`Z=(PV_(m))/(RT)=1-(a)/(RT)`

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The correct Answer is:
To derive the reduced form of the Van der Waals equation at low pressure, we can follow these steps: ### Step-by-Step Solution: 1. **Start with the Van der Waals Equation**: The Van der Waals equation for one mole of a gas is given by: \[ \left( P + \frac{a}{V_m^2} \right) (V_m - b) = RT \] where \( P \) is the pressure, \( V_m \) is the molar volume, \( a \) and \( b \) are Van der Waals constants, \( R \) is the universal gas constant, and \( T \) is the temperature in Kelvin. 2. **Consider Low Pressure**: At low pressure, the volume \( V_m \) becomes much larger than the constant \( b \) (the excluded volume). Therefore, we can approximate: \[ V_m - b \approx V_m \] This simplification allows us to ignore the volume correction due to the size of the molecules. 3. **Substitute the Approximation into the Equation**: Substituting this approximation into the Van der Waals equation gives: \[ \left( P + \frac{a}{V_m^2} \right) V_m = RT \] 4. **Rearranging the Equation**: Expanding this equation, we have: \[ P V_m + \frac{a}{V_m} = RT \] Rearranging gives: \[ P V_m = RT - \frac{a}{V_m} \] 5. **Divide by RT**: Dividing the entire equation by \( RT \) yields: \[ \frac{P V_m}{RT} = 1 - \frac{a}{RT V_m} \] 6. **Define the Compressibility Factor (Z)**: The compressibility factor \( Z \) is defined as: \[ Z = \frac{PV_m}{RT} \] Thus, we can rewrite the equation as: \[ Z = 1 - \frac{a}{RT V_m} \] 7. **Conclusion**: Therefore, at low pressure, the Van der Waals equation reduces to: \[ Z = 1 - \frac{a}{RT V_m} \]
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