Why does nitrogen gas' pressure not change after an addition of helium

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SUMMARY

The discussion centers on the behavior of nitrogen and helium gases in a closed system when additional helium is introduced. Initially, a 9 L vessel contains 3 moles each of helium and nitrogen at 10 atm, resulting in partial pressures of 5 atm for both gases. Upon adding 2 moles of helium, the total pressure increases to 12.2 atm, but the partial pressure of nitrogen remains unchanged at 5 atm due to the ideal gas law, which states that the partial pressure of a gas is determined solely by its own mole fraction in the mixture. This behavior is attributed to the assumptions of ideal gas behavior, which neglects intermolecular interactions and particle volume.

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a 9 L vessel contains 3 moles of helium and 3 moles of nitrogen at a pressure of 10 atm. Maintaining constant temperature, an additional 2 moles of helium are added. Assuming gases behave ideally, what are the partial pressures of nitrogen and helium at the end?

Initially there's: 3mol He/(3mol + 3mol) * 10 atm = 5 atm pressure of He
And: 3/6 * 10atm = 5 atm pressure of N2 as well

now that 2 moles of He are added to the vessel, why wouldn't N2's partial pressure increase? The way I see it, there are now more atoms, so more of them would knock on the walls, therefore pressure would increase overall, and since there are now more atoms, space between atoms is tightened, so ...
Anyway, overall pressure is P1/n1 = P2/n2
(10 atm/9 mol) = (P2/11 mol); P2 = 12.2 atm new total pressure
Partial PHe * Ptotal = 5/11 * 12.2 atm = 5.545 atm He
That's for He gas, but why shouldn't partial pressure change for N2 gas?
 
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There are the same amount of nitrogen molecules so the nitrogen partial pressure does not change. Your total pressure is wrong. Where did 9 and 11 come from?
 
This comes from the assumption of ideal gas behavior. The partial pressure of an ideal gas is the pressure of the same amount of the pure gas at the same temperature/volume as in the mixture. Ideal gases are assumed to have zero intermolecular interactions and particle volume, this greatly simplifies a lot of the mathematics and is a very good approximation to small (mon- and diatomic) gases at fairly low pressures. The greater the pressure or the larger the gas the greater the deviation from ideality which necessitates the use of "messy" http://www.chem.arizona.edu/~salzmanr/480a/480ants/VIRIAL/virial.html or Van der Waals equation to account for the intermolecular forces and non-negligible particle volume.

I'd recommend getting comfortable with the assumptions underlying the concept of an ideal gas.
 

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