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Electrolysis and Electrolytes

During electr...

Question

During electrolysis, $O_{2} (g)$ is evolved at anode in
$⎡ ⎢ ⎢ ⎢ ⎢ ⎢ ⎣ \begin{matrix} (c o r r e c t) C u (s) ⟶ & C u^{2 +} (a q) + 2 e^{-} E_{C u | C u^{2 +}}^{⊝} = - 0.34 V (w r o n g) 2 H_{2} O (l) ⟶ & O_{2} (g) + 4 H^{\oplus} (a q) + 4 e^{-} E_{H_{2} O | O_{2}}^{⊝} = - 1.23 V \end{matrix} ⎤ ⎥ ⎥ ⎥ ⎥ ⎥ ⎦$

$\begin{matrix} I n (d) \end{matrix}$ $⎡ ⎢ ⎢ ⎢ ⎢ ⎢ ⎢ ⎢ ⎢ ⎣ \begin{matrix} (c o r r e c t) N i (s) ⟶ & N i^{2 +} (a q) + 2 e^{-} E_{N i | N i^{2 +}}^{⊝} = - 0.25 V (w r o n g) 4 ⊝ O H (a q) ⟶ & O_{2} (g) + 2 H_{2} O (l) + 4 e^{-} E_{⊝ O H | O_{2}}^{\oplus} = - 0.4 V \end{matrix} ⎤ ⎥ ⎥ ⎥ ⎥ ⎥ ⎥ ⎥ ⎥ ⎦$

A

Dilute

H_{2} S O_{4}

with Pt electrode

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B

Aqueous

A g N O_{3}

with Pt electrode

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C

Dilute

H_{2} S O_{4}

with Cu electrode

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D

Fused NaOH with an cathode and Ni anode

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Solution

The correct options are
A Dilute $H_{2} S O_{4}$ with Pt electrode
B Aqueous $A g N O_{3}$ with Pt electrode
As the oxidation potential of $E_{H_{2} O | O_{2}}$ is -1.23 V which is lesser compared to $N i$ and $C u$ oxidation potential, $O_{2}$ will no be evolved at $N i$ and $C u$ electrode.

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Similar questions

Q. In the electrolytic refining of copper using

C u S O_{4}

as the electrolyte, the anode reaction is

Q. Consider a galvanic cell using solid

C u

F e

metals with their corresponding solutions.
What is the

E_{c e l l}^{\circ}

Standard Potential (V)	Reduction Half-Reaction
$2.87$	$F_{2} (g) + 2 e^{-} \to 2 F^{-} (a q)$
$1.51$	$M n O_{4}^{-} (a q) + 8 H^{+} (a q) + 5 e^{-} \to M n^{2 +} (a q) + 4 H_{2} O (l)$
$1.36$	$C l_{2} (a q) + 3 e^{-} \to 2 C l^{-} (a q)$
$1.33$	$C r_{2} O_{7}^{2 -} (a q) + 14 H^{+} (a q) + 6 e^{-} \to 2 C r^{3 +} (a q) + 7 H_{2} O (l)$
$1.23$	$O_{2} (g) + 4 H^{+} (a q) + 4 e^{-} \to 2 H_{2} O (l)$
$1.06$	$B r_{2} (l) + 2 e^{-} \to 2 B r^{-} (a q)$
$0.96$	$N O_{3}^{-} (a q) + 4 H^{+} (a q) + 3 e^{-} \to N O (g) + H_{2} O (l)$
$0.80$	$A g^{+} (a q) + e^{-} \to A g (s)$ $
$0.77$	$F e^{3 +} (a q) + e^{-} \to F e^{2 +} (a q)$
$0.68$	$O_{2} (g) + 2 H^{+} (a q) + 2 e^{-} \to H_{2} O_{2} (a q)$
$0.59$	$M n O_{4}^{-} (a q) + 2 H_{2} O (l) + 3 e^{-} \to M n O_{2} (s) + 4 O H^{-} (a q)$
$0.54$	$I_{2} (s) + 2 e^{-} \to 2 I^{-} (a q)$
$0.40$	$O_{2} (g) + 2 H_{2} O (l) + 4 e^{-} \to 4 O H^{-} (a q)$
$0.34$	$C u^{2 +} (a q) + 2 e^{-} \to C u (s)$
$0$	$2 H^{+} (a q) + 2 e^{-} \to H_{2} (g)$
$- 0.28$	$N i^{2 +} (a q) + 2 e^{-} \to N i (s)$
$- 0.44$	$F e^{2 +} (a q) + 2 e^{-} \to F e (s)$
$- 0.76$	$Z n^{2 +} (a q) + 2 e^{-} \to Z n (s)$
$- 0.83$	$2 H_{2} O (l) + 2 e^{-} \to H_{2} (g) + 2 O H^{-} (a q)$
$1.66$	$A l^{3 +} (a q) + 3 e^{-} \to A l (s)$
$- 2.71$	$N a^{+} (a q) + e^{-} \to N a (s)$
$- 3.05$	$L i^{+} (a q) + e^{-} \to L i (s)$

Q. Consider a spontaneous electrochemical cell between

C u

A l

. Predict what would happen if excess concentrated

N a O H

were added to the cell with copper ions and a precipitate forms.

Standard Potential (V)	Reduction Half-Reaction
$2.87$	$F_{2} (g) + 2 e^{-} \to 2 F^{-} (a q)$
$1.51$	$M n O_{4}^{-} (a q) + 8 H^{+} (a q) + 5 e^{-} \to M n^{2 +} (a q) + 4 H_{2} O (l)$
$1.36$	$C l_{2} (a q) + 3 e^{-} \to 2 C l^{-} (a q)$
$1.33$	$C r_{2} O_{7}^{2 -} (a q) + 14 H^{+} (a q) + 6 e^{-} \to 2 C r^{3 +} (a q) + 7 H_{2} O (l)$
$1.23$	$O_{2} (g) + 4 H^{+} (a q) + 4 e^{-} \to 2 H_{2} O (l)$
$1.06$	$B r_{2} (l) + 2 e^{-} \to 2 B r^{-} (a q)$
$0.96$	$N O_{3}^{-} (a q) + 4 H^{+} (a q) + 3 e^{-} \to N O (g) + H_{2} O (l)$
$0.80$	$A g^{+} (a q) + e^{-} \to A g (s)$ $
$0.77$	$F e^{3 +} (a q) + e^{-} \to F e^{2 +} (a q)$
$0.68$	$O_{2} (g) + 2 H^{+} (a q) + 2 e^{-} \to H_{2} O_{2} (a q)$
$0.59$	$M n O_{4}^{-} (a q) + 2 H_{2} O (l) + 3 e^{-} \to M n O_{2} (s) + 4 O H^{-} (a q)$
$0.54$	$I_{2} (s) + 2 e^{-} \to 2 I^{-} (a q)$
$0.40$	$O_{2} (g) + 2 H_{2} O (l) + 4 e^{-} \to 4 O H^{-} (a q)$
$0.34$	$C u^{2 +} (a q) + 2 e^{-} \to C u (s)$
$0$	$2 H^{+} (a q) + 2 e^{-} \to H_{2} (g)$
$- 0.28$	$N i^{2 +} (a q) + 2 e^{-} \to N i (s)$
$- 0.44$	$F e^{2 +} (a q) + 2 e^{-} \to F e (s)$
$- 0.76$	$Z n^{2 +} (a q) + 2 e^{-} \to Z n (s)$
$- 0.83$	$2 H_{2} O (l) + 2 e^{-} \to H_{2} (g) + 2 O H^{-} (a q)$
$1.66$	$A l^{3 +} (a q) + 3 e^{-} \to A l (s)$
$- 2.71$	$N a^{+} (a q) + e^{-} \to N a (s)$
$- 3.05$	$L i^{+} (a q) + e^{-} \to L i (s)$

Q. Calculate the

E

E^{\circ}

N i | N i^{2 +} | | C u^{2 +} | C u

from the following half-cell reactions:

N i^{2 +} + 2 e^{-} \to N i; E^{\circ} = - 0.25 v o l t

C u^{2 +} + 2 e^{-} \to C u; E^{\circ} = + 0.34 v o l t

[N i^{2 +}] = 1 M

[C u^{2 +}] = 10^{- 3} M)

Q. In a hydrogen oxygen fuel cell, electricity is produced. In this process

H_{2} (g)

is oxidised at anode and

O_{2} (g)

reduced at cathode. Given : Cathode:

O_{2} (g) + 2 H_{2} O (l) + 4 e^{-} \to 4 O H^{-} (a q)

H_{2} (g) + 2 O H^{-} (a q) \to 2 H_{2} O (l) + 2 e^{-}

4.48 L

H_{2}

1 atm

273 K

9650 sec

.
If current produced in fuel cell, use for the deposition of

C u^{2 +}

1 L

2 M C u S O_{4} (aq)

241.25 sec

P t

p H

of solution after electrolysis is:

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