One mole of an ideal gas does 3000 J of work on its surroundings as it expands isothermally to a final pressure of 1.00 atm and volume of 250 L. What is the initial volume and the temperature of the gas?

Answer 1

First, let's note a few important conditions:

  • Isothermal means the temperature is held constant, so #color(green)(DeltaT = 0)#.

    In these conditions, there is no change in enthalpy #DeltaH# nor any change in internal energy #DeltaU#. Not sure if we need it, but we should know that #color(blue)(DeltaH = DeltaU = 0)# for an ideal gas if #DeltaT = 0#.

    • We are given final pressure but not initial pressure, and final volume but not initial volume. So, we would probably have to manipulate the Ideal Gas Law #PV = nRT# for #T#, and maybe something to do with the work function for #V_1#.

      REVERSIBLE WORK VS VOLUME

      Now, we should know that reversible (efficient) work is defined as:

      #\mathbf(w_"rev" = -intPdV)#

      For this problem, the depiction in a PV-diagram goes like this:

      However, since we do not know #DeltaP# and the equation had assumed that #DeltaP = 0# (note that we are integrating with respect to volume, not pressure), we have use the Ideal Gas Law to rewrite the above equation as:

      #w_"rev" = -int_(V_1)^(V_2)(nRT)/VdV#

      Since #DeltaT = 0#, #nRT# is a constant. Let's pull it out of the integral.

      #w_"rev" = -nRTint_(V_1)^(V_2)1/VdV#

      #= -nRTln|V_2/V_1|#

      At this point, the shape of the PV-diagram curve looks sensible; it resembles the shape of a #-lnx# curve.

      THE INITIAL VOLUME FOR THE EXPANSION

      We are given the work, so we should be able to solve for the initial volume, #V_1#, using this equation. Since expansion work has been done by the gas, meaning that #V_2 > V_1#, we know that #color(green)(w_"rev" < 0)#, numerically.

      That makes sense because #ln|V_2/V_1|# when #V_2/V_1 > 1# is positive. Now let's get an expression for #V_1#.

      #-w_"rev"/(nRT) = ln|V_2/V_1|#

      #e^(-w_"rev""/"nRT) = V_2/V_1#

      #e^(w_"rev""/"nRT) = V_1/V_2#

      #color(green)(V_1 = V_2e^(w_"rev""/"nRT))#

      However, we do not know the temperature yet, so we'll have to put off calculating the initial volume for a bit longer.

      THE TEMPERATURE FOR THE EXPANSION

      Something we do know is that the temperature remained constant, so #T_2 = T_1#. Thus, we have these two relationships that cover the initial and final states:

      #P_1V_1 = color(blue)(nR)T#
      #color(blue)(P_2V_2) = color(blue)(nR)T#

      We know the values of what is in blue, which is enough.

      #color(blue)(T) = (P_2V_2)/(nR) = (("1 atm")("250 L"))/(("1 mol")("0.082057 L"cdot"atm/mol"cdot"K"))#

      #=# #color(blue)("3046.66 K")#

      Now we can find the initial volume:

      #color(blue)(V_1) = ("250 L")e^((-"3000 J")"/"[("1 mol")("8.314472 J/mol"cdot"K")("3046.66 K")]#

      #=# #color(blue)("222.08 L")#

      (As an aside, if you were curious, the initial pressure was about #"1.126 atm"#, from the Ideal Gas Law.)

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Answer 2

The initial volume (( V_i )) and the temperature (( T )) of the gas can be calculated using the ideal gas law and the work done equation for an isothermal process.

Given:

  • Work done (( W )) = 3000 J
  • Final pressure (( P_f )) = 1.00 atm
  • Final volume (( V_f )) = 250 L

Using the ideal gas law ( PV = nRT ), where ( n ) is the number of moles, we can rearrange it to find ( n ): [ n = \frac{PV}{RT} ]

Since the process is isothermal, the temperature (( T )) remains constant. Thus, ( T ) is the same at both initial and final states.

Then, we can find the initial volume (( V_i )) using the work done equation for an isothermal process: [ W = nRT\ln\left(\frac{V_f}{V_i}\right) ]

Rearranging this equation to solve for ( V_i ), we get: [ V_i = V_f \exp\left(-\frac{W}{nRT}\right) ]

Substituting the values and solving for ( V_i ): [ V_i = 250 \times \exp\left(-\frac{3000}{nRT}\right) ]

Once ( V_i ) is found, you can use the ideal gas law to find the temperature ( T ) at either the initial or final state.

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Answer from HIX Tutor

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

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