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AveGali [126]
3 years ago
5

A certain half-reaction has a standard reduction potential +0.80 V . An engineer proposes using this half-reaction at the anode

of a galvanic cell that must provide at least 0.9 V of electrical power. The cell will operate under standard conditions. Note for advanced students: assume the engineer requires this half-reaction to happen at the anode of the cell.
a. Is there a minimum standard reduction potential that the half-reaction used at the cathode of this cell can have?
b. Is there a maximum standard reduction potential that the half-reaction used at the cathode of this cell can have?
Chemistry
1 answer:
Strike441 [17]3 years ago
8 0

Answer:

a. Minimum 1.70 V

b. There is no maximum.

Explanation:

We can solve this question by remembering that the cell potential is given by the formula

ε⁰ cell = ε⁰ reduction -  ε⁰  oxidation

Now the problem states the cell must provide at least 0.9 V and that the reduction potential of the  oxidized species  0.80 V, thus

ε⁰ reduction -  ε⁰  oxidation ≥  ε⁰ cell

Since ε⁰  oxidation is by definition the negative of ε⁰ reduction , we have

ε⁰ reduction - ( 0.80 V )  ≥  0.90 V

⇒ ε⁰ reduction  ≥ 1.70 V

Therefore,

(a) The minimum standard reduction potential is 1.70 V

(b) There is no maximum standard reduction potential since it is stated in the question that we want to have a cell that provides at leat 0.9 V

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A beaker with 155 mL of an acetic acid buffer with a pH of 5.000 is sitting on a benchtop. The total molarity of acid and conjug
OverLord2011 [107]

Answer:

ΔpH = 0.296

Explanation:

The equilibrium of acetic acid (CH₃COOH) in water is:

CH₃COOH ⇄ CH₃COO⁻ + H⁺

Henderson-Hasselbalch formula to find pH in a buffer is:

pH = pKa + log₁₀ [CH₃COO⁻] / [CH₃COOH]

Replacing with known values:

5.000 = 4.740 + log₁₀ [CH₃COO⁻] / [CH₃COOH]

0.260 =  log₁₀ [CH₃COO⁻] / [CH₃COOH]

1.820 = [CH₃COO⁻] / [CH₃COOH] <em>(1)</em>

As total molarity of buffer is 0.100M:

[CH₃COO⁻] + [CH₃COOH] = 0.100M <em>(2)</em>

Replacing (2) in (1):

1.820 = 0.100M - [CH₃COOH] / [CH₃COOH]

1.820[CH₃COOH] = 0.100M - [CH₃COOH]

2.820[CH₃COOH] = 0.100M

[CH₃COOH] = 0.100M / 2.820

[CH₃COOH] = <em>0.035M</em>

Thus: [CH₃COO⁻] = 0.100M - 0.035M = <em>0.065M</em>

5.40 mL of a 0.490 M HCl are:

0.0054L × (0.490mol / L) = 2.646x10⁻³ moles HCl.

Moles of CH₃COO⁻ are: 0.155L × (0.065mol / L) = 0.0101 moles

HCl reacts with CH₃COO⁻ thus:

HCl + CH₃COO⁻ → CH₃COOH

After reaction, moles of CH₃COO⁻ are:

0.0101 moles - 2.646x10⁻³ moles = <em>7.429x10⁻³ moles of CH₃COO⁻</em>

<em />

Moles of CH₃COOH  before reaction are: 0.155L × (0.035mol / L) = 5.425x10⁻³ moles of CH₃COOH. As reaction produce 2.646x10⁻³ moles of CH₃COOH, final moles are:

5.425x10⁻³ moles +  2.646x10⁻³ moles = <em>8.071x10⁻³ moles of CH₃COOH</em>. Replacing these values in Henderson-Hasselbalch formula:

pH = 4.740 + log₁₀ [7.429x10⁻³ moles] / [8.071x10⁻³ moles]

pH = 4.704

As initial pH was 5.000, change in pH is:

ΔpH = 5.000 - 4.740 = <em>0.296</em>

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