Irreversible isothermal Process Work External pressure not provided

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Aurelius120
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Homework Statement
An ideal gas is irreversibly isothermally expanded from ##(8bar ,4L)##to##(2bar,16L)##to##(1bar,32L) ##Find heat.
Relevant Equations
NA
Text problem: One mole of an ideal monoatomic gas expanded irreversibly in two-stage expansion. State 1 (8.0 bar, 4.0 litre, 300K), State 2 (2.0 bar, 16 litre, 300K), State 3 (1.0 bar, 32 litre, 300K). Total heat absorbed by the gas in the process is:

It is clear that the process is isothermal else it is not possible to find heat absorbed.
$$W=-P_{ext}(\Delta V)$$

However ##P_{ext}## is not given. How do I proceed?
I tried taking ##W=-(P_2V_2-P_1V_1+P_3V_3-P_2V_2)=\Delta(PV)## but it is wrong for obvious reasons.
 
The one solution I found uses
##W_1=-(2)(16-4)## and ##W_2=-(1)(32-16)##
##W=(W_1+W_2) bar.Litre=-4000J##
And ##Q=4000J##

How external pressure becomes ##2\ bar## and ##1\ bar## is beyond me. It also seems wrong that ##P_{ext}## should change in an irreversible process? That is like the only thing that is good about irreversible calculations.
 
Mister T said:
Sketch a PV diagram of the process. Do you know what an isotherm looks like for an ideal gas?
PV diagram of an isothermal expansion: a decreasing green curve from point i at high pressure, small volume, to point f at lower pressure, larger volume; the area under the curve is shaded, labelled W > 0, with W(i→f) = nRT ln(Vf/Vi).

Something like this correct?
 
Looks like you've found the way!
Aurelius120 said:
How external pressure becomes ##2\ bar## and ##1\ bar## is beyond me.
A slow compression expansion.

Aurelius120 said:
It also seems wrong that ##P_{ext}## should change in an irreversible process?
A dramatic example would be an explosion.
 
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