Respuesta :
Answer:
a) so for this process q = -w = 1573.25J, ( deltaH = 0 )
b) q = -w = - ( - 1135.68J ) = 1135.68J
c) q = 0
Explanation:
Given that;
Moles of Ar gas is 1.00 mol
a)
isothermal i.e constant temperature expansion of ideal gas deltaU = 0
now since deltaU = 0 = q + w
0 = q + w
q = -w
now for isothermal reversible expansion.
w = -nRTin(Vf/Vt)
= (1.00mol) ( 8.314K^-1.mol^-1) (273K) in(44.8L/22.4L)
= - 1573.25J
so for this process q = -w = 1573.25J
for a perfect gas at constant temperature, deltaH = 0
dH = D( U + PV )
so at constant temperature dU = 0
and PV = constant for perfect gas; d(PV) = 0
THEREfore deltaH = 0
b)
For isothermal i.e constant temperature expansion of ideal gas
deltaU = 0
for a perfect gas at constant temp deltaH = 0
final pressure of the gas in this case is calculated using ideal gas equation
p = nRT/V
we know that {1pa=1Jm^-3}
= [((1.00mol) ( 8.314K^-1.mol^-1) (273K))/(44.8L)] * (1000 Lm^-3)
= 5.07 * 10^4 Pa
for expansion against an external pressure
w = - Pext . deltav
= - (5.07 * 10^4 Pa) ( 44.8L - 22.4L) (1m^3 / 1000L)
= - 1135.68J
q = -w = - ( - 1135.68J ) = 1135.68J
c)
For this scenerio,
deltaU = 0 and deltaH = 0
for free expansion Pext. = 0
therefore Pext * deltaV = 0 * ( 44.8L - 22.4L) = 0
since q = -w, for this process, q = 0