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Redox Reactions and Electrochemistry: Chemistry | JEE Main Consider the cell
P t ( s ) ∣ H 2 ( g ) ( 1 a t m ) ∣ H + ( a q , [ H + ] = 1 ) ∥ F e 3 + ( a q ) , F e 2 + ( a q ) ∣ P t ( s ) \mathrm{Pt}(\mathrm{s})\mid\mathrm{H}_2(\mathrm{g})(1\mathrm{~atm})\mid\mathrm{H}^{+}(\mathrm{aq},[\mathrm{H}^{+}]=1)\parallel\mathrm{Fe}^{3+}(\mathrm{aq}), \mathrm{Fe}^{2+}(\mathrm{aq})\mid\mathrm{Pt}(\mathrm{s}) Pt ( s ) ∣ H 2 ( g ) ( 1 atm ) ∣ H + ( aq , [ H + ] = 1 ) ∥ Fe 3 + ( aq ) , Fe 2 + ( aq ) ∣ Pt ( s ) Given
E F e 3 + / F e 2 + ∘ = 0.771 V \mathrm{E}_{\mathrm{Fe}^{3+}/\mathrm{Fe}^{2+}}^{\circ}=0.771\mathrm{~V} E Fe 3 + / Fe 2 + ∘ = 0.771 V and
E H + / 1 / 2 H 2 ∘ = 0 V , T = 298 K \mathrm{E}_{\mathrm{H}^{+}/1/2\mathrm{H}_2}^{\circ}=0\mathrm{~V}, \mathrm{T}=298\mathrm{~K} E H + /1/2 H 2 ∘ = 0 V , T = 298 K
If the potential of the cell is
0.712 V 0.712\mathrm{~V} 0.712 V , the ratio of concentration of
F e 2 + \mathrm{Fe}^{2+} Fe 2 + to
F e 3 + \mathrm{Fe}^{3+} Fe 3 + is (Nearest integer)
Hint 1 of 3
What is the overall spontaneous cell reaction for this electrochemical cell?
1 2 H 2 ( g ) + F e 3 + ( a q ) → H + ( a q ) + F e 2 + ( a q ) \frac{1}{2}\mathrm{H}_2(\mathrm{g}) + \mathrm{Fe}^{3+}(\mathrm{aq}) \rightarrow \mathrm{H}^{+}(\mathrm{aq}) + \mathrm{Fe}^{2+}(\mathrm{aq}) 2 1 H 2 ( g ) + Fe 3 + ( aq ) → H + ( aq ) + Fe 2 + ( aq ) H + ( a q ) + F e 2 + ( a q ) → 1 2 H 2 ( g ) + F e 3 + ( a q ) \mathrm{H}^{+}(\mathrm{aq}) + \mathrm{Fe}^{2+}(\mathrm{aq}) \rightarrow \frac{1}{2}\mathrm{H}_2(\mathrm{g}) + \mathrm{Fe}^{3+}(\mathrm{aq}) H + ( aq ) + Fe 2 + ( aq ) → 2 1 H 2 ( g ) + Fe 3 + ( aq ) No score. Commit to your first instinct. We’ll show what your mind noticed and what it missed.
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The ratio of concentration of F e 2 + \mathrm{Fe}^{2+} Fe 2 + to F e 3 + \mathrm{Fe}^{3+} Fe 3 + is 10. Option analysis
Why each option works or fails
Step Working
01 given Cell: P t ( s ) ∣ H 2 ( 1 atm ) ∣ H + ( 1 M ) ∥ F e 3 + , F e 2 + ∣ P t ( s ) \mathrm{Pt}(\mathrm{s})\mid\mathrm{H}_2(1\text{ atm})\mid\mathrm{H}^{+}(1\text{ M})\parallel\mathrm{Fe}^{3+},\mathrm{Fe}^{2+}\mid\mathrm{Pt}(\mathrm{s}) Pt ( s ) ∣ H 2 ( 1 atm ) ∣ H + ( 1 M ) ∥ Fe 3 + , Fe 2 + ∣ Pt ( s ) , E F e 3 + / F e 2 + ∘ = 0.771 V E^\circ_{\mathrm{Fe}^{3+}/\mathrm{Fe}^{2+}} = 0.771\text{ V} E Fe 3 + / Fe 2 + ∘ = 0.771 V , E H + / 1 2 H 2 ∘ = 0 V E^\circ_{\mathrm{H}^+/\frac{1}{2}\mathrm{H}_2} = 0\text{ V} E H + / 2 1 H 2 ∘ = 0 V , E cell = 0.712 V E_{\text{cell}} = 0.712\text{ V} E cell = 0.712 V at T = 298 K T = 298\text{ K} T = 298 K .
02 find The ratio of concentration of F e 2 + \mathrm{Fe}^{2+} Fe 2 + to F e 3 + \mathrm{Fe}^{3+} Fe 3 + , i.e., [ F e 2 + ] / [ F e 3 + ] [\mathrm{Fe}^{2+}]/[\mathrm{Fe}^{3+}] [ Fe 2 + ] / [ Fe 3 + ] .
03 strategise 1. Write the half-cell reactions and the net cell reaction:
Anode: 1 2 H 2 ( g ) → H + ( a q ) + e − \frac{1}{2}\mathrm{H}_2(\mathrm{g}) \rightarrow \mathrm{H}^+(\mathrm{aq}) + \mathrm{e}^- 2 1 H 2 ( g ) → H + ( aq ) + e −
Cathode: F e 3 + ( a q ) + e − → F e 2 + ( a q ) \mathrm{Fe}^{3+}(\mathrm{aq}) + \mathrm{e}^- \rightarrow \mathrm{Fe}^{2+}(\mathrm{aq}) Fe 3 + ( aq ) + e − → Fe 2 + ( aq )
Overall: 1 2 H 2 ( g ) + F e 3 + ( a q ) → H + ( a q ) + F e 2 + ( a q ) \frac{1}{2}\mathrm{H}_2(\mathrm{g}) + \mathrm{Fe}^{3+}(\mathrm{aq}) \rightarrow \mathrm{H}^+(\mathrm{aq}) + \mathrm{Fe}^{2+}(\mathrm{aq}) 2 1 H 2 ( g ) + Fe 3 + ( aq ) → H + ( aq ) + Fe 2 + ( aq ) with n = 1 n = 1 n = 1 .
2. Calculate E cell ∘ = E cathode ∘ − E anode ∘ = 0.771 − 0 = 0.771 V E^\circ_{\text{cell}} = E^\circ_{\text{cathode}} - E^\circ_{\text{anode}} = 0.771 - 0 = 0.771\text{ V} E cell ∘ = E cathode ∘ − E anode ∘ = 0.771 − 0 = 0.771 V .
3. Apply the Nernst equation at 298 K 298\text{ K} 298 K :
E cell = E cell ∘ − 0.0591 n log Q E_{\text{cell}} = E^\circ_{\text{cell}} - \frac{0.0591}{n} \log Q E cell = E cell ∘ − n 0.0591 log Q
Here, Q = [ F e 2 + ] [ H + ] [ F e 3 + ] P H 2 1 / 2 = [ F e 2 + ] [ F e 3 + ] Q = \frac{[\mathrm{Fe}^{2+}][\mathrm{H}^+]}{[\mathrm{Fe}^{3+}] P_{\mathrm{H}_2}^{1/2}} = \frac{[\mathrm{Fe}^{2+}]}{[\mathrm{Fe}^{3+}]} Q = [ Fe 3 + ] P H 2 1/2 [ Fe 2 + ] [ H + ] = [ Fe 3 + ] [ Fe 2 + ] since [ H + ] = 1 [\mathrm{H}^+] = 1 [ H + ] = 1 and P H 2 = 1 atm P_{\mathrm{H}_2} = 1\text{ atm} P H 2 = 1 atm .
04 execute Substitute the numerical values into the Nernst equation:
0.712 = 0.771 − 0.059 log [ F e 2 + ] [ F e 3 + ] 0.712 = 0.771 - 0.059 \log \frac{[\mathrm{Fe}^{2+}]}{[\mathrm{Fe}^{3+}]} 0.712 = 0.771 − 0.059 log [ Fe 3 + ] [ Fe 2 + ]
0.059 log [ F e 2 + ] [ F e 3 + ] = 0.771 − 0.712 = 0.059 0.059 \log \frac{[\mathrm{Fe}^{2+}]}{[\mathrm{Fe}^{3+}]} = 0.771 - 0.712 = 0.059 0.059 log [ Fe 3 + ] [ Fe 2 + ] = 0.771 − 0.712 = 0.059
log [ F e 2 + ] [ F e 3 + ] = 1 \log \frac{[\mathrm{Fe}^{2+}]}{[\mathrm{Fe}^{3+}]} = 1 log [ Fe 3 + ] [ Fe 2 + ] = 1
[ F e 2 + ] [ F e 3 + ] = 10 1 = 10 \frac{[\mathrm{Fe}^{2+}]}{[\mathrm{Fe}^{3+}]} = 10^1 = 10 [ Fe 3 + ] [ Fe 2 + ] = 1 0 1 = 10
✓ verify Checking the direction of cell potential: E cell = 0.712 V < E cell ∘ = 0.771 V E_{\text{cell}} = 0.712\text{ V} < E^\circ_{\text{cell}} = 0.771\text{ V} E cell = 0.712 V < E cell ∘ = 0.771 V , which means Q > 1 Q > 1 Q > 1 . Hence, the ratio [ F e 2 + ] / [ F e 3 + ] = 10 > 1 [\mathrm{Fe}^{2+}]/[\mathrm{Fe}^{3+}] = 10 > 1 [ Fe 2 + ] / [ Fe 3 + ] = 10 > 1 , which is completely consistent.
Hints that build this answer step by step What is the overall spontaneous cell reaction for this electrochemical cell?
1 2 H 2 ( g ) + F e 3 + ( a q ) → H + ( a q ) + F e 2 + ( a q ) \frac{1}{2}\mathrm{H}_2(\mathrm{g}) + \mathrm{Fe}^{3+}(\mathrm{aq}) \rightarrow \mathrm{H}^{+}(\mathrm{aq}) + \mathrm{Fe}^{2+}(\mathrm{aq}) 2 1 H 2 ( g ) + Fe 3 + ( aq ) → H + ( aq ) + Fe 2 + ( aq ) Which form of the Nernst equation applies to this cell at 298 K 298\text{ K} 298 K , where n = 1 n = 1 n = 1 , [ H + ] = 1 [\mathrm{H}^+] = 1 [ H + ] = 1 , and P H 2 = 1 atm P_{\mathrm{H}_2} = 1\text{ atm} P H 2 = 1 atm ?
E cell = E cell ∘ − 0.0591 log 10 ( [ F e 2 + ] [ F e 3 + ] ) E_{\text{cell}} = E^\circ_{\text{cell}} - 0.0591\log_{10}\left(\frac{[\mathrm{Fe}^{2+}]}{[\mathrm{Fe}^{3+}]}\right) E cell = E cell ∘ − 0.0591 log 10 ( [ Fe 3 + ] [ Fe 2 + ] ) Substitute E cell = 0.712 V E_{\text{cell}} = 0.712\text{ V} E cell = 0.712 V and E cell ∘ = 0.771 V E^\circ_{\text{cell}} = 0.771\text{ V} E cell ∘ = 0.771 V into the equation to find [ F e 2 + ] [ F e 3 + ] \frac{[\mathrm{Fe}^{2+}]}{[\mathrm{Fe}^{3+}]} [ Fe 3 + ] [ Fe 2 + ] . What is the value?
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Question type Numerical
Exam relevance JEE Main · Chemistry
Concepts assessed Chemistry
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Editorial review 8 September 2026 Quick checks
Students also ask Why do we use 0.059 instead of 0.0591 or 2.303 RT/F? At 298 K, 2.303 RT/F evaluates to ~0.0591 V. Here, 0.771 - 0.712 = 0.059 V, which is designed by the examiner to cancel directly with 0.059.
Answer The ratio of concentration of F e 2 + \mathrm{Fe}^{2+} Fe 2 + to F e 3 + \mathrm{Fe}^{3+} Fe 3 + is 10.
Why each option works or fails Step-by-step solution given: Cell: P t ( s ) ∣ H 2 ( 1 atm ) ∣ H + ( 1 M ) ∥ F e 3 + , F e 2 + ∣ P t ( s ) \mathrm{Pt}(\mathrm{s})\mid\mathrm{H}_2(1\text{ atm})\mid\mathrm{H}^{+}(1\text{ M})\parallel\mathrm{Fe}^{3+},\mathrm{Fe}^{2+}\mid\mathrm{Pt}(\mathrm{s}) Pt ( s ) ∣ H 2 ( 1 atm ) ∣ H + ( 1 M ) ∥ Fe 3 + , Fe 2 + ∣ Pt ( s ) , E F e 3 + / F e 2 + ∘ = 0.771 V E^\circ_{\mathrm{Fe}^{3+}/\mathrm{Fe}^{2+}} = 0.771\text{ V} E Fe 3 + / Fe 2 + ∘ = 0.771 V , E H + / 1 2 H 2 ∘ = 0 V E^\circ_{\mathrm{H}^+/\frac{1}{2}\mathrm{H}_2} = 0\text{ V} E H + / 2 1 H 2 ∘ = 0 V , E cell = 0.712 V E_{\text{cell}} = 0.712\text{ V} E cell = 0.712 V at T = 298 K T = 298\text{ K} T = 298 K . find: The ratio of concentration of F e 2 + \mathrm{Fe}^{2+} Fe 2 + to F e 3 + \mathrm{Fe}^{3+} Fe 3 + , i.e., [ F e 2 + ] / [ F e 3 + ] [\mathrm{Fe}^{2+}]/[\mathrm{Fe}^{3+}] [ Fe 2 + ] / [ Fe 3 + ] . strategise: 1. Write the half-cell reactions and the net cell reaction:
Anode: 1 2 H 2 ( g ) → H + ( a q ) + e − \frac{1}{2}\mathrm{H}_2(\mathrm{g}) \rightarrow \mathrm{H}^+(\mathrm{aq}) + \mathrm{e}^- 2 1 H 2 ( g ) → H + ( aq ) + e −
Cathode: F e 3 + ( a q ) + e − → F e 2 + ( a q ) \mathrm{Fe}^{3+}(\mathrm{aq}) + \mathrm{e}^- \rightarrow \mathrm{Fe}^{2+}(\mathrm{aq}) Fe 3 + ( aq ) + e − → Fe 2 + ( aq )
Overall: 1 2 H 2 ( g ) + F e 3 + ( a q ) → H + ( a q ) + F e 2 + ( a q ) \frac{1}{2}\mathrm{H}_2(\mathrm{g}) + \mathrm{Fe}^{3+}(\mathrm{aq}) \rightarrow \mathrm{H}^+(\mathrm{aq}) + \mathrm{Fe}^{2+}(\mathrm{aq}) 2 1 H 2 ( g ) + Fe 3 + ( aq ) → H + ( aq ) + Fe 2 + ( aq ) with n = 1 n = 1 n = 1 .
2. Calculate E cell ∘ = E cathode ∘ − E anode ∘ = 0.771 − 0 = 0.771 V E^\circ_{\text{cell}} = E^\circ_{\text{cathode}} - E^\circ_{\text{anode}} = 0.771 - 0 = 0.771\text{ V} E cell ∘ = E cathode ∘ − E anode ∘ = 0.771 − 0 = 0.771 V .
3. Apply the Nernst equation at 298 K 298\text{ K} 298 K :
E cell = E cell ∘ − 0.0591 n log Q E_{\text{cell}} = E^\circ_{\text{cell}} - \frac{0.0591}{n} \log Q E cell = E cell ∘ − n 0.0591 log Q
Here, Q = [ F e 2 + ] [ H + ] [ F e 3 + ] P H 2 1 / 2 = [ F e 2 + ] [ F e 3 + ] Q = \frac{[\mathrm{Fe}^{2+}][\mathrm{H}^+]}{[\mathrm{Fe}^{3+}] P_{\mathrm{H}_2}^{1/2}} = \frac{[\mathrm{Fe}^{2+}]}{[\mathrm{Fe}^{3+}]} Q = [ Fe 3 + ] P H 2 1/2 [ Fe 2 + ] [ H + ] = [ Fe 3 + ] [ Fe 2 + ] since [ H + ] = 1 [\mathrm{H}^+] = 1 [ H + ] = 1 and P H 2 = 1 atm P_{\mathrm{H}_2} = 1\text{ atm} P H 2 = 1 atm . execute: Substitute the numerical values into the Nernst equation:
0.712 = 0.771 − 0.059 log [ F e 2 + ] [ F e 3 + ] 0.712 = 0.771 - 0.059 \log \frac{[\mathrm{Fe}^{2+}]}{[\mathrm{Fe}^{3+}]} 0.712 = 0.771 − 0.059 log [ Fe 3 + ] [ Fe 2 + ]
0.059 log [ F e 2 + ] [ F e 3 + ] = 0.771 − 0.712 = 0.059 0.059 \log \frac{[\mathrm{Fe}^{2+}]}{[\mathrm{Fe}^{3+}]} = 0.771 - 0.712 = 0.059 0.059 log [ Fe 3 + ] [ Fe 2 + ] = 0.771 − 0.712 = 0.059
log [ F e 2 + ] [ F e 3 + ] = 1 \log \frac{[\mathrm{Fe}^{2+}]}{[\mathrm{Fe}^{3+}]} = 1 log [ Fe 3 + ] [ Fe 2 + ] = 1
[ F e 2 + ] [ F e 3 + ] = 10 1 = 10 \frac{[\mathrm{Fe}^{2+}]}{[\mathrm{Fe}^{3+}]} = 10^1 = 10 [ Fe 3 + ] [ Fe 2 + ] = 1 0 1 = 10 verify: Checking the direction of cell potential: E cell = 0.712 V < E cell ∘ = 0.771 V E_{\text{cell}} = 0.712\text{ V} < E^\circ_{\text{cell}} = 0.771\text{ V} E cell = 0.712 V < E cell ∘ = 0.771 V , which means Q > 1 Q > 1 Q > 1 . Hence, the ratio [ F e 2 + ] / [ F e 3 + ] = 10 > 1 [\mathrm{Fe}^{2+}]/[\mathrm{Fe}^{3+}] = 10 > 1 [ Fe 2 + ] / [ Fe 3 + ] = 10 > 1 , which is completely consistent.