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Rashid [163]
2 years ago
6

Phosphorus pentafluoride, PF5, acts as a __________ during the formation of the anion PF−6. Select the correct answer below: A.

Lewis acid B. Lewis base C. catalyst D. drying agent
Chemistry
1 answer:
vodomira [7]2 years ago
3 0

Answer:

Lewis acid

Explanation:

In chemistry, a Lewis acid is any chemical specie that accepts a lone pair of electrons while a Lewis base is any chemical specie that donates a lone pair of electrons.

If we look at the formation of PF6^-, the process is as follows;

PF5 + F^- -----> PF6^-

We can see that PF5 accepted a lone pair of electrons from F^- making PF5 a lewis acid according to our definition above.

Hence in the formation of PF6^-, PF5 acts a Lewis acid.

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Functional groups create active sites in molecules. The polar part of a molecule that can hydrogen bond to water is said be hydr
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Polar/Hydrophilic

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3 years ago
Convert 19 kcal into joules
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Question 3 When the population size decreases over time, the total number of births the total number of deaths. O less than O eq
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Sulfuric acid is produced in larger amounts by weight than any other chemical. It is used in manufacturing fertilizers, oil refi
Fed [463]

Answer:

A. -166.6 kJ/mol

B. -127.7 kJ/mol

C. -133.9 kJ/mol

Explanation:

Let's consider the oxidation of sulfur dioxide.

2 SO₂(g) + O₂(g) → 2 SO₃(g)     ΔG° = -141.8 kJ

The Gibbs free energy (ΔG) can be calculated using the following expression:

ΔG = ΔG° + R.T.lnQ

where,

ΔG° is the standard Gibbs free energy

R is the ideal gas constant

T is the absolute temperature (25 + 273.15 = 298.15 K)

Q is the reaction quotient

The molar concentration of each gas ([]) can be calculated from its pressure (P) using the following expression:

[]=\frac{P}{R.T}

<em>Calculate ΔG at 25°C given the following sets of partial pressures.</em>

<em>Part A  130atm SO₂, 130atm O₂, 2.0atm SO₃. Express your answer using four significant figures.</em>

[SO_{2}]=[O_{2}]=\frac{130atm}{(0.08206atm.L/mol.K).298K} =5.32M

[SO_{3}]=\frac{2.0atm}{(0.08206atm.L/mol.K).298K} =0.0818M

Q=\frac{[SO_3]^{2} }{[SO_{2}]^{2}.[O_{2}] } =\frac{0.0818^{2} }{5.32^{3} } =4.44 \times 10^{-5}

ΔG = ΔG° + R.T.lnQ = -141.8 kJ/mol + (8.314 × 10⁻³ kJ/mol.K) × 298 K × ln (4.44 × 10⁻⁵) = -166.6 kJ/mol

<em>Part B  5.0atm SO₂, 3.0atm O₂, 30atm SO₃  Express your answer using four significant figures.</em>

<em />

[SO_{2}]=\frac{5.0atm}{(0.08206atm.L/mol.K).298K}=0.204M

[O_{2}]=\frac{3.0atm}{(0.08206atm.L/mol.K).298K}=0.123M

[SO_{3}]=\frac{30atm}{(0.08206atm.L/mol.K).298K}=1.23M

Q=\frac{[SO_3]^{2} }{[SO_{2}]^{2}.[O_{2}] } =\frac{1.23^{2} }{0.204^{2}.0.123 } =296

ΔG = ΔG° + R.T.lnQ = -141.8 kJ/mol + (8.314 × 10⁻³ kJ/mol.K) × 298 K × ln 296 = -127.7 kJ/mol

<em>Part C Each reactant and product at a partial pressure of 1.0 atm.  Express your answer using four significant figures.</em>

<em />

[SO_{2}]=[O_{2}]=[SO_{3}]=\frac{1.0atm}{(0.08206atm.L/mol.K).298K}=0.0409M

Q=\frac{[SO_3]^{2} }{[SO_{2}]^{2}.[O_{2}] } =\frac{0.0409^{2} }{0.0409^{3}} =24.4

ΔG = ΔG° + R.T.lnQ = -141.8 kJ/mol + (8.314 × 10⁻³ kJ/mol.K) × 298 K × ln 24.4 = -133.9 kJ/mol

7 0
3 years ago
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