Answer:
The correct answer is 146 g/mol
Explanation:
<em>Freezing point depression</em> is a colligative property related to the number of particles of solute dissolved in a solvent. It is given by:
ΔTf = Kf x m
Where ΔTf is the freezing point depression (in ºC), Kf is a constant for the solvent and m is the molality of solution. From the problem, we know the following data:
ΔTf = 1.02ºC
Kf = 5.12ºC/m
From this, we can calculate the molality:
m = ΔTf/Kf = 1.02ºC/(5.12ºC/m)= 0.199 m
The molality of a solution is defined as the moles of solute per kg of solvent. Thus, we can multiply the molality by the mass of solvent in kg (250 g= 0.25 kg) to obtain the moles of solute:
0.199 mol/kg benzene x 0.25 kg = 0.0498 moles solute
There are 0.0498 moles of solute dissolved in the solution. To calculate the molar mass of the solute, we divide the mass (7.27 g) into the moles:
molar mass = mass/mol = 7.27 g/(0.0498 mol) = 145.9 g/mol ≅ 146 g/mol
<em>Therefore, the molar mass of the compound is 146 g/mol </em>
2.4(10^3)
=2.4*10^3
=2.4*(10*10*10)
=2400 <span>milliliters
To </span>centiliters is<span> 2400mL= <u>240.0000cl. </u> </span>
To test if the hypothesis is correct, a good way is to think of it this way:
Density = mass/volume, right?
Calculate the mass and volume of each and do the equation; this will test your hypothesis.
You will be left with the density of each. But, make sure that the sample sizes are the same (controlled variable) otherwise it will be an unfair test.
Explanation:
Given
The enthalpy of formation of RbF (s) is –557.7kJ/mol
The standard enthalpy of formation of RbF (aq, 1 m) is –583.8 kJ/mol
The enthalpy of solution of RbF = Enthalpy of RbF (aq) - Enthalpy of formation of RbF (s)
= -583.8 - (-557.7) kJ/mol
= -26.1 kJ/mol
The enthalpy is negative which means that the temperature will rise when RbF is dissolved.
Answer:
![[Ag^{+}]=4.2\times 10^{-2}M](https://tex.z-dn.net/?f=%5BAg%5E%7B%2B%7D%5D%3D4.2%5Ctimes%2010%5E%7B-2%7DM)
Explanation:
Given:
[AgNO3] = 0.20 M
Ba(NO3)2 = 0.20 M
[K2CrO4] = 0.10 M
Ksp of Ag2CrO4 = 1.1 x 10^-12
Ksp of BaCrO4 = 1.1 x 10^-10

![Ksp=[Ba^{2+}][CrO_{4}^{2-}]](https://tex.z-dn.net/?f=Ksp%3D%5BBa%5E%7B2%2B%7D%5D%5BCrO_%7B4%7D%5E%7B2-%7D%5D)
![1.2\times 10^{-10}=(0.20)[CrO_{4}^{2-}]](https://tex.z-dn.net/?f=1.2%5Ctimes%2010%5E%7B-10%7D%3D%280.20%29%5BCrO_%7B4%7D%5E%7B2-%7D%5D)
![[CrO_{4}^{2-}]=\frac{1.2\times 10^{-10}}{(0.20)}= 6.0\times 10^{-10}](https://tex.z-dn.net/?f=%5BCrO_%7B4%7D%5E%7B2-%7D%5D%3D%5Cfrac%7B1.2%5Ctimes%2010%5E%7B-10%7D%7D%7B%280.20%29%7D%3D%206.0%5Ctimes%2010%5E%7B-10%7D)
Now,

![Ksp=[Ag^{+}]^{2}[CrO_{4}^{2-}]](https://tex.z-dn.net/?f=Ksp%3D%5BAg%5E%7B%2B%7D%5D%5E%7B2%7D%5BCrO_%7B4%7D%5E%7B2-%7D%5D)
![1.1\times 10^{-12}=[Ag^{+}]^{2}](6.0\times 10^{-10})](https://tex.z-dn.net/?f=1.1%5Ctimes%2010%5E%7B-12%7D%3D%5BAg%5E%7B%2B%7D%5D%5E%7B2%7D%5D%286.0%5Ctimes%2010%5E%7B-10%7D%29)
![[Ag^{+}]^{2}]=\frac{1.1\times 10^{-12}}{(6.0\times 10^{-10})}= 1.8\times 10^{-3}](https://tex.z-dn.net/?f=%5BAg%5E%7B%2B%7D%5D%5E%7B2%7D%5D%3D%5Cfrac%7B1.1%5Ctimes%2010%5E%7B-12%7D%7D%7B%286.0%5Ctimes%2010%5E%7B-10%7D%29%7D%3D%201.8%5Ctimes%2010%5E%7B-3%7D)
![[Ag^{+}]=\sqrt{1.8\times 10^{-3}}=4.2\times 10^{-2}M](https://tex.z-dn.net/?f=%5BAg%5E%7B%2B%7D%5D%3D%5Csqrt%7B1.8%5Ctimes%2010%5E%7B-3%7D%7D%3D4.2%5Ctimes%2010%5E%7B-2%7DM)
So, BaCrO4 will start precipitating when [Ag+] is 4.2 x 1.2^-2 M