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Corrosion

Rusting on th...

Question

Rusting on the surface of iron involves:

A

F e (s) \to F e^{2 +} (a q .) + 2 e^{-}

(at anodic site)

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B

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

(at cathodic site)

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C

4 F e^{2 +} (a q .) + O_{2} (g) + 4 H_{2} O (l) \to 2 F e_{2} O_{3} (s) + 8 H^{+}

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D

F e_{2} O_{3} (s) + x H_{2} O (l) \to F e_{2} O_{3} \cdot x H_{2} O

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Solution

The correct option is D $F e (s) \to F e^{2 +} (a q .) + 2 e^{-}$ (at anodic site)
Rusting or corrosion is a redox reaction in which the metal atoms oxidize to metal ions. When water is in contact with the surface of iron atoms in the presence of oxygen, it forms a simple chemical cell voltaic cell.

At the anode (surface of iron in contact with water: Iron ( $F e$ ) oxidizes to form iron (II) ions ( $F e^{+} 2$ ) by releasing electrons.

$F e \to F e^{+ 2} + 2 e^{-}$ .

Hence, the correct option is $A$

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Q. Assertion :The rusting on the surface of iron involves following reaction :
a.

F e (s) \to F e^{2 +} (a q) + 2 e^{-}

(at anodic site)
b.

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

(at cathodic site)
c.

4 F e^{2 +} (a q) + O_{2} (g) + 4 H_{2} O (l) \to 2 F e_{2} O_{3} (s) + 8 H^{\oplus}

F e_{2} O_{3} (a q) + x H_{2} O (l) \to F e_{2} O_{3} . x H_{2} O

Reason: Rusting is accelerated in the presence of

N a C l

C O_{2}

Read the above assertion and reason and choose the correct option regarding it.

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. 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} ⎤ ⎥ ⎥ ⎥ ⎥ ⎥ ⎥ ⎥ ⎥ ⎦

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. The reaction,

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

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