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The van der Waal's constants a & b of CO...

The van der Waal's constants a & b of `CO_(2)` are `3.64 L^(2) mol^(-2)` bar & `0.04 L mol^(-1)` respectively. The value of `R` is `0.083 bar dm^(3)mol^(-1)K^(-1)`. If one mole of `CO_(2)` is confined to a volume of `0.15L at 300 K`, then the pressure (in bar) eaxerted by the gas is :

A

`11 bar`

B

`64.58 bar`

C

`174.50 bar`

D

`135.78 bar`

Text Solution

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To solve the problem, we will use the Van der Waals equation for real gases, which is given by: \[ \left( P + \frac{a}{V^2} \right) (V - b) = nRT \] Where: - \( P \) = pressure of the gas - \( a \) = Van der Waals constant for attraction (given as \( 3.64 \, \text{L}^2 \text{mol}^{-2} \text{bar} \)) - \( b \) = Van der Waals constant for volume occupied by gas molecules (given as \( 0.04 \, \text{L mol}^{-1} \)) - \( V \) = volume of the gas (given as \( 0.15 \, \text{L} \)) - \( n \) = number of moles of gas (given as \( 1 \, \text{mol} \)) - \( R \) = universal gas constant (given as \( 0.083 \, \text{bar dm}^3 \text{mol}^{-1} \text{K}^{-1} \)) - \( T \) = temperature (given as \( 300 \, \text{K} \)) ### Step 1: Substitute the known values into the Van der Waals equation. We start with the equation: \[ \left( P + \frac{3.64}{(0.15)^2} \right) (0.15 - 0.04) = 1 \times 0.083 \times 300 \] ### Step 2: Calculate the term \( \frac{a}{V^2} \). Calculating \( \frac{3.64}{(0.15)^2} \): \[ (0.15)^2 = 0.0225 \] \[ \frac{3.64}{0.0225} = 161.78 \, \text{bar} \] ### Step 3: Calculate \( V - b \). Calculating \( 0.15 - 0.04 \): \[ 0.15 - 0.04 = 0.11 \, \text{L} \] ### Step 4: Calculate \( nRT \). Calculating \( 1 \times 0.083 \times 300 \): \[ 0.083 \times 300 = 24.9 \, \text{bar} \] ### Step 5: Substitute the calculated values back into the equation. Now substituting back into the equation: \[ \left( P + 161.78 \right) (0.11) = 24.9 \] ### Step 6: Expand and rearrange the equation to solve for \( P \). Expanding the left side: \[ 0.11P + 17.7958 = 24.9 \] Rearranging gives: \[ 0.11P = 24.9 - 17.7958 \] Calculating the right side: \[ 0.11P = 7.1042 \] ### Step 7: Solve for \( P \). Now, divide by \( 0.11 \): \[ P = \frac{7.1042}{0.11} = 64.58 \, \text{bar} \] ### Final Answer: Thus, the pressure exerted by the gas is approximately: \[ P \approx 64.58 \, \text{bar} \]

To solve the problem, we will use the Van der Waals equation for real gases, which is given by: \[ \left( P + \frac{a}{V^2} \right) (V - b) = nRT \] Where: - \( P \) = pressure of the gas ...
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