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
Answer:
A and D are true , while B and F statements are false.
Explanation:
A) True. Since the standard gibbs free energy is
ΔG = ΔG⁰ + RT*ln Q
where Q= [P1]ᵃ.../([R1]ᵇ...) , representing the ratio of the product of concentration of chemical reaction products P and the product of concentration of chemical reaction reactants R
when the system reaches equilibrium ΔG=0 and Q=Keq
0 = ΔG⁰ + RT*ln Q → ΔG⁰ = (-RT*ln Keq)
therefore the first equation also can be expressed as
ΔG = RT*ln (Q/Keq)
thus the standard gibbs free energy can be determined using Keq
B) False. ΔG⁰ represents the change of free energy under standard conditions . Nevertheless , it will give us a clue about the ΔG around the standard conditions .For example if ΔG⁰>>0 then is likely that ΔG>0 ( from the first equation) if the temperature or concentration changes are not very distant from the standard conditions
C) False. From the equation presented
ΔG⁰ = (-RT*ln Keq)
ΔG⁰>0 if Keq<1 and ΔG⁰<0 if Keq>1
for example, for a reversible reaction ΔG⁰ will be <0 for forward or reverse reaction and the ΔG⁰ will be >0 for the other one ( reverse or forward reaction)
D) True. Standard conditions refer to
T= 298 K
pH= 7
P= 1 atm
C= 1 M for all reactants
Water = 55.6 M
Answer:
CHO
Explanation:
Carbon = 41%, Hydrogen = 4.58%, oxygen = 54.6%
Step 1:
Divide through by their respective relative atomic masses
41/ 12, 4.58/1, 54.6/16
3.41 4.58 3.41
Step 2:
Divide by the lowest ratio:
3.41/3.41, 4.58/3.41, 3.41/3.41
1, 1, 1
Hence the empirical formula is CHO