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Lemur [1.5K]
3 years ago
12

Water has the following thermodynamic values: ΔH°fus of H2O = 6.02 kJ/mol ΔH°vap of H2O = 40.7 kJ/mol heat capacity of solid H2O

= 2.09 J/g°C heat capacity of liquid H2O = 4.18 J/g°C heat capacity of gaseous H2O = 1.97 J/g°C
How much energy (in kJ) is required to raise the temperature of 25.0 g of H2O from -129°C to 262°C?
Enter your answer in units of kJ to three significant figures.
Chemistry
1 answer:
Brrunno [24]3 years ago
8 0

Answer:

Qtotal = 90.004 kJ

Explanation:

To start resolving the problem we need to first convert the kJ/mol units from the thermodynamic values to J/g, so that we can work with the units of the heat capacity values. We know that the molar mass of water is 18.015 g/mol, so with this we do the respective conversion:

ΔH°fus of H2O = (6.02 kJ/mol) (1 mol/18.015g) (1000J/kJ) = 334.165 J/g

ΔH°vap of H2O = (40.7 kJ/mol) (1mol/18.015g) (1000J/kJ) = 2259.228 J/g

Now we need to find out the heat energy required to rise the temperature (specific heat capacity) and the energy required for each change of phase (specific latent heat), and add everything up. For this we will require the specific heat capacity and latent heat equations:

Q = mCΔT ; where m = mass, C = Hear capacity, ΔT = change of temperature

Q = mL ; where m = mass, L = specific latent heat

<u />

<u>First change of phase (solid to liquid - fusion)</u>

Q1 = (25g) (2.09 J/g°C) (0°C - (-129°C) = 6740.25 J

Q2 = (25g) (334.165 J/g) = 8354.125 J

<u>Second change of phase (liquid to gas - vaporization)</u>

Q3 = (25g) (4.18 J/g°C) (100°C - 0°C = 10450 J

Q4 = (25g) (2259.228 J/g) = 56480.7 J

<u>Rise of temperature of the gaseous water</u>

Q5 = (25g) (1.97 J/g°C) (262°C - 100°C = 7978.5 J

Finally we add everything up:

Qtotal = Q1 + Q2 + Q3 + Q4 + Q5 = 6740.25 J + 8354.125 J + 10450 J + 56480.7 J + 7978.5 J = 90003.575 J = 90.004 kJ

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Aloiza [94]

Answer:

To determine the enthalpy and entropy of dissolving a compound, you need to measure the Ksp at multiple temperatures. Then, plot ln(Ksp) vs. 1/T. The slope of the plotted line relates to the enthalpy (ΔH) of dissolving and the intercept of the plotted line relates to the entropy (ΔS) of dissolving.

Explanation:

Hello there!

In this case, according to the given information, it turns out possible for us use the thermodynamic definition of the Gibbs free energy and its relationship with Ksp as follows:

\Delta G=-RTln(Ksp)\\\\\Delta G=\Delta H-T\Delta S

Thus, by combining them, we obtain:

-RTln(Ksp)=\Delta H-T\Delta S\\\\ln(Ksp)=-\frac{\Delta H}{RT} +\frac{T\Delta S}{RT} \\\\ln(Ksp)=-\frac{\Delta H}{RT} +\frac{\Delta S}{R}

Which is related to the general line equation:

y=mx+b

Whereas:

y=ln(Ksp)\\\\m=-\frac{\Delta H}{R} \\\\x=\frac{1}{T} \\\\b=\frac{\Delta S}{R}

It means that we answer to the blanks as follows:

To determine the enthalpy and entropy of dissolving a compound, you need to measure the Ksp at multiple temperatures. Then, plot ln(Ksp) vs. 1/T. The slope of the plotted line relates to the enthalpy (ΔH) of dissolving and the intercept of the plotted line relates to the entropy (ΔS) of dissolving.

Regards!

8 0
3 years ago
How many molecules in 4.10 mol H2O?
Shtirlitz [24]

Answer:

2,47 * 10^{24} (molecules)

Explanation:

Avogadro's number is a very important relationship: 1 mole = 6,02 * 10^{23} atoms, molecules, protons, etc.

To convert from moles to molecules, multiply the molar amount by Avogadro's number.

4,1 mol * 6,02 * 10^{23}  ≈ 24,7 * 10^{23} = 2,47 * 10^{24} (molecules)

Therefore the third answer is correct

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Answer:

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The idea of recrystallization works when the solubility of the target substance decreases as the temperature of the solution decreases.

The method of recrystallization involves dissolving the solute in a suitable hot solvent and then allow the solution to cool gradually. The pure solute dissolves in the hot solvent and then separates out of the solution as it is cooled to room temperature.

Hence recrystallization is preferred over solvent extraction when the desired compound is poorly soluble in the solvent pair at low temperatures and greatly soluble in the solvent pair at high temperatures.

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