To calculate the work done on the gas during the expansion, you can use the formula:
W=−PΔVW = -P Delta VW=−PΔV
where:
- WWW represents the work done on the gas,
- PPP is the pressure of the gas, and
- ΔVDelta VΔV is the change in volume of the gas.
In this case, since the gas is an ideal gas, we can use the ideal gas law to determine the pressure. The ideal gas law states:
PV=nRTPV = nRTPV=nRT
where:
- PPP is the pressure,
- VVV is the volume,
- nnn is the number of moles of gas,
- RRR is the ideal gas constant (0.0821 L·atm/(mol·K)), and
- TTT is the temperature in Kelvin.
Given that the temperature is 0.0°C, we need to convert it to Kelvin:
T=0.0°C+273.15=273.15KT = 0.0°C + 273.15 = 273.15 KT=0.0°C+273.15=273.15K
Now, we can calculate the initial pressure of the gas using the ideal gas law. Since the number of moles is 1.0 mol and the volume is 3.0 L, we have:
P_1 = frac{{nRT}}{{V}} = frac{{(1.0 , ext{mol})(0.0821 , ext{L} cdot ext{atm/(mol} cdot ext{K)}})(273.15 , ext{K})}}{{3.0 , ext{L}}}
Simplifying the expression, we get:
P1≈7.16 atmP_1 approx 7.16 , ext{atm}P1≈7.16atm
Next, we calculate the final pressure of the gas using the same formula, but with the final volume of 10.0 L:
P_2 = frac{{(1.0 , ext{mol})(0.0821 , ext{L} cdot ext{atm/(mol} cdot ext{K)}})(273.15 , ext{K})}}{{10.0 , ext{L}}}
Simplifying the expression, we get:
P2≈2.46 atmP_2 approx 2.46 , ext{atm}P2≈2.46atm
Now that we have the initial and final pressures, as well as the change in volume, we can calculate the work done on the gas: