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Electrochemistry Practice Problems Guide

The document contains daily practice problems and solutions related to electrochemistry for NEET preparation. It covers various concepts such as molar conductance, Gibbs free energy, electrode potentials, and fuel cells, providing specific equations and calculations. Each problem is followed by its corresponding answer, aiding in the understanding of electrochemical principles.

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0% found this document useful (0 votes)
15 views5 pages

Electrochemistry Practice Problems Guide

The document contains daily practice problems and solutions related to electrochemistry for NEET preparation. It covers various concepts such as molar conductance, Gibbs free energy, electrode potentials, and fuel cells, providing specific equations and calculations. Each problem is followed by its corresponding answer, aiding in the understanding of electrochemical principles.

Uploaded by

Sowmy B
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

DPP FOR NEET

DAILY PRACTICE PROBLEMS


Ch 17: Electrochemistry
Solutions

1. (c) At infinite dilution each ion makes a definite contribution towards


molar conductance which is given by

2. (d) Degree of dissociation,

3. (a)
4. (d) Standard Gibbs free energy is given as ∆G° = – nE°F
If < 0 i.e., – ve
∆G° > 0
Further ∆G° = – RT ln Keq
∴ ∆G° > 0 and Keq < 1
5. (b) ; Eº = – 0.44

The metals having higher negative electrode potential values can


displace metals having lower values of negative electrode potential
from their salt solutions.

6. (d)

7. (b)

For concentration cell,


In it R, T, n and F are constant
So E is based upon

Now =

= –RTlnC2/C1
At constant temperature is based upon ln (C2/C1).
8. (b) For Zn2+ → Zn

9. (a) The given order of reduction potentials (or tendencies) is Z > Y >
X. A spontaneous reaction will have the following characteristics
Z reduced and Y oxidised
Z reduced and X oxidised
Y reduced and X oxidised
Hence, Y will oxidise X and not Z.
10. (b) For, , 0.44 – 0.33 = 0.11V is positive,
hence reaction is spontaneous.
11. (a) will oxidise ion according to the equation

The cell corresponding to this reaction is as follows:

1.51 -1.40 = 0.11 V


being +ve, will be -ve and hence the above reaction is
feasible. will not only oxidise ion but also ion
simultaneously.
12. (b) Conductivity (X) = conductance (c) × cell constant
Cell constant =

Conductivity of NaOH = .Z

m (NaOH) =

13. (c) From the given data we find Fe3+ is strongest oxidising agent.
More the positive value of E°, more is the tendency to get
oxidized. Thus correct option is (c).
14. (a) In case of molar conductance of strong electrolyte there is little
increase with dilution.
15. (d) A device that converts energy of combustion of fuels, directly into
electrical energy is known as fuel cell.

16. (d) E =

E= 0.0592 × 2
= 0. 118 × 1 = 0.118V
17. (b) In fuel cell, the combustion of H2 occurs to create
potential difference between the two electrodes
18. (a) H2 2H+ + 2e–
1 atm 10–10

=0– log

= +0.59 V
19. (b) HCl completely dissociates to give H+ and ions, hence act as
very good electrolyte. While others are non- electrolytes.
20. (d) Kohlrausch’s Law states that at infinite dilution, each ion migrates
independently of its co-ion and contributes to the total equivalent
conductance of an electrolyte a definite share which depends only
on its own nature.
From this definition we can see that option (d) is the correct answer.
21. (212.3) ∆G = –nF E°cell = –2 × 96500 × 1.1 J = 212.3 kJ.
22. (1.096) Writing the equation for pentane-oxygen fuel cell at respective
electrodes and overall reaction, we get
At Anode:

At Cathode:

Calculation of ∆G° for the above reaction


∆G° = [5×(–394.4) + 6× (–237.2)]
– [–8.2]
= – 1972.0 – 1423.2 + 8.2 = – 3387.0 kJ
= – 3387000 Joules.
From the equation we find n = 32
Using the relation, ∆G° = – and substituting various values, we
get
– 3387000 = –32×96500× (F = 96500C)

or

= or V = 1.0968 V

23. (97) CH3OH (l) + O2 (g) → CO2 (g) + 2H2O (l)

= – 394.4 + 2 (–237.2) – (–166.2) – 0


= – 394.4 – 474.4 + 166.2 = – 702.6 k J
% efficiency =

24. (1) 112 ml of H2 at STP =

(Since 22400 ml at STP = [Link])


Amount deposited

25. (1.567) Here n = 4, and [H+] = 10– 3 (as pH = 3)


Applying Nernst equation

E = Eº –

= 1.67 – 0.103 = 1.567 V

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