Considering ideal gas:
PV= RTn
T= 25.2°C = 298.2 K
P1= 637 torr = 0.8382 atm
V1= 536 mL = 0.536 L
:. R=0.082 atm.L/K.mol
:. n= (P1V1)/(RT) = ((0.8382 atm) x (0.536 L))/
((0.082 atmL/Kmol) x (298.2K))
:. n= O.0184 mol
Then,
P2= 712 torr = 0.936842 atm
V2 = RTn/P2 = [(0.082atmL/
Kmol) x (298.2K) x (0.0184mol) ]/(0.936842atm)
:.V2 = 0.4796 L
OR
V2 = 479.6 ml
Answer:
w = -531 kJ
1. Work was done by the system.
Explanation:
Step 1: Given data
- Heat gained by the system (q): 687 kJ (By convention, when the system absorbs heat, q > 0).
- Change in the internal energy of the system (ΔU°): 156 kJ
Step 2: Calculate the work done (w)
We will use the following expression.
ΔU° = q + w
w = ΔU° - q
w = 156 kJ - 687 kJ
w = -531 kJ
By convention, when w < 0, work is done by the system on the surroundings.
I think it’s 1 mole
If Iam not mistaken
Answer:
Mole fraction of solute is 0.0462
Explanation:
To solve this we use the colligative property of lowering vapor pressure.
First of all, we search for vapor pressure of pure water at 25°C = 23.8 Torr
Now, we convert the Torr to mmHg. Ratio is 1:1, so 23.8 Torr is 23.8 mmHg.
Formula for lowering vapor pressure is:
ΔP = P° . Xm
Where ΔP = P' (Vapor pressure of solution) - P° (Vapor pressure of pure solvent)
Xm = mole fraction
24.9 mmHg - 23.8 mmHg = 23mmHg . Xm
Xm = (24.9 mmHg - 23.8 mmHg) / 23mmHg
Xm = 0.0462