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True [87]
2 years ago
11

Use the thermodynamic data at 298 k below to determine the ksp for barium carbonate, baco3 at this temperature. substance: ba2+(

aq) co32–(aq) baco3(s) δh°f (kj/mol): –538.36 –676.26 –1219 δg°f (kj/mol): –560.7 –528.1 –1139 s°(j/k·mol): 13 –53.1 112
Chemistry
1 answer:
jeka57 [31]2 years ago
8 0

Answer : the correct answer for ksp = 1.59 * 10⁻⁹

Following are the steps to calculate the ksp of reaction

BaCO₃ →Ba ²⁺ + CO₃²⁻ :

Step 1 : To find ΔG° of reaction :

ΔG° of reaction can be calculates by taking difference between ΔG° of products and reactants as :

ΔG° reaction =Sum of ΔG° ( products ) - Sum of Δ G° ( reactants ) .

Given : ΔG° for Ba²⁺ ( product )= -560.7 \frac{KJ}{Mol}

ΔG° for CO₃²⁻ (product ) =- 528.1 \frac{KJ}{Mol}

ΔG° BaCO₃ ( reactant) = –1139 \frac{KJ}{Mol}

Plugging value in formula :

ΔG° for reaction = ( ΔG° of Ba ²⁺ + ΔG° of CO₃²⁻ ) - (ΔG° of BaCO₃ )

⁻ = ( -560.7 \frac{KJ}{Mol} + 528.1 \frac{KJ}{Mol} ) - ( -1139 \frac{KJ}{Mol} )

= ( -1088.8 \frac{KJ}{Mol}) - (-1139 \frac{KJ}{Mol} )

= - 1088.8 \frac{KJ}{Mol} + 1139 \frac{KJ}{Mol}

ΔG° of reaction = 50.2 \frac{KJ}{Mol}

Step 2: To calculate ksp from ΔG° of reaction .

The relation between Ksp and ΔG° is given as :

ΔG° = -RT ln ksp

Where ΔG° = Gibb's Free energy R = gas constant T = Temperature

Ksp = Solubility constant product .

Given : ΔG° of reaction = 50.2 \frac{KJ}{Mol}

T = 298 K R = 8.314 \frac{J}{Mol * K}

Plugging values in formula

50.2 \frac{KJ}{mol}  =  -  8.314 \frac{J}{mol * K} * 298 K * ln  ksp

50.2 \frac{KJ}{mol}  =  - 2477.572 \frac{J}{mol} * ln K

((Converting 2477 \frac{J}{mol}  to \frac{KJ}{mol}

Since , 1 KJ = 1000 J So , 2477 \frac{J}{mol}  * \frac{1 KJ}{1000J}  = 2.477 \frac{KJ}{mol} ))

Dividing both side by - 2.477 \frac{KJ}{mol}

\frac{50.2\frac{KJ}{mol}}{-2.477 \frac{KJ}{mol}} = \frac{-2.477 \frac{KJ}{mol}}{-2.477 \frac{KJ}{mol}} * ln ksp

ln ksp = ln ksp = -20.27 \frac{KJ}{mol}

Removing ln :

ksp = 1. 59 * 10⁻⁹

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<h3>Answer:</h3>

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                                  Formal Charge  =  [5] - [2 + 6/2]

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Answer:

1. 90%

2. 217.4 g O₂

3. 95.0%

4. Trial 2 ratios

Explanation:

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Balanced: SiCl₄ + O₂ → SiO₂ + 2Cl₂

Trial        SiCl₄                   O₂                    SiO₂

 1           120 g                  240 g              38.2 g

 2           75 g                   50 g                25.2 g

<u>Percentage yield for trial 1</u>

We need to get actual yield (38.2 g) and theoretical yield, in grams.

Mass to moles:

 molar mass SiCl₄: 28.09 + 4(35.45) = 169.9 g/mol

 120 g SiCl₄ x 1 mol/169.9 g = .706 mol SiCl₄

Moles to moles:

 For each mole SiCl₄, we have one mol SiO₂ based on the balanced rxn.

 .706 mol SiCl₄ = .706 mol SiO₂

Moles to mass:

 molar mass SiO₂: 28.09 + 2(16.00) = 60.09 g/mol

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Theoretical yield:

 actual/theoretical x 100

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<u>Leftover reactant for trial 1</u>

We know oxygen is the excess reactant.

Mass to moles:

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 240 g O₂ x 1 mol/32.00 g = 7.5 mol O₂

We used .706 mol SiO₂, so we also used .706 mol O₂.

 7.5 - .706 = 6.8 moles left over

Moles to mass:

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<u />

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 75 g SiCl₄ x 1 mol/169.9 g = .441 mol SiCl₄

Moles to moles:

 For each mole SiCl₄, we have one mol SiO₂ based on the balanced rxn.

 .441 mol SiCl₄ = .441 mol SiO₂

Moles to mass:

 molar mass SiO₂: 60.09 g/mol

 .441 mol SiO₂ x 60.09g/mol = 26.5 g SiO₂

Theoretical yield:

 actual/theoretical x 100

 25.2 / 26.5 = .950 = <u>95.0% yield</u>

Because the percentage yield of trial 2 is higher than that of trial 1, we know that the ratio of reactants in trial 2 is more efficient! We got a result closer to our theoretical yield.

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