Electrochemistry Mock Test – Class 12 Chemistry
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Electrochemistry Mock Test – Class 12 Chemistry

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Electrochemistry – Progressive Test

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1. Combining the equilibrium condition with the Nernst equation gives:

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2. Use the four arrangements below.
Case P: in and in , with an external wire and an ionic connection.
Case Q: in and in , with neither connection.
Case R: Two electrodes in identical solutions.
Case S: and placed in separate dry, empty beakers.
The arrangement representing a complete Daniell cell is:

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3. A graph shows conductance on the vertical axis and temperature on the horizontal axis. Curve P slopes downward for a metal, while curve Q slopes upward for an electrolyte solution over the same moderate temperature range. The best interpretation is:

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4. A one-electron reaction at has . Its equilibrium constant is:

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5. An initially blue aqueous solution is electrolysed with inert electrodes. After some time, the cathode is coated with a reddish-brown solid, bubbles appear at the anode, the blue colour becomes paler, and the pH falls. The best explanation is:

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6. During discharge of a lead storage cell, the electrode materials and electrolyte are:

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7. Assertion: Standard electrode potentials alone may not predict the observed electrolysis product correctly.
Reason: Concentration, electrode material, and overvoltage can alter the relative ease of competing electrode processes.

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8. Select the row that consistently relates cell potential, Gibbs-energy change, and reaction tendency.

Row Thermodynamic condition
P Positive Positive Forward reaction spontaneous
Q Negative Negative Forward reaction spontaneous
R Zero Negative Equilibrium
S Positive Negative Forward reaction spontaneous

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9. Equal-concentration aqueous solutions of and are compared at the same temperature. The solution normally has higher conductivity because:

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10. A nickel-cadmium rechargeable cell uses:

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11. The thermodynamic relation connecting the Gibbs-energy change of a reversible cell reaction with its cell potential is:

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12. Assertion: A concentration cell tends to reduce the concentration difference between its two half-cells.
Reason: Oxidation occurs in the dilute half-cell, while reduction occurs in the concentrated half-cell.

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13. The spontaneous tendency responsible for Daniell-cell operation is represented by:

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14. The same solution has conductivity . Cell P has cell constant , while Cell Q has cell constant . Their measured resistances are:

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15. At a specified temperature, and . The limiting molar conductivity of is:

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16. In acidic representation, the cathodic half-reaction during electrolysis of acidified water is:

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17. An ideal battery has a capacity of . If it supplies a constant current of , the expected operating time is:

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18. Conductivity data for a sparingly soluble salt give its molar solubility through:

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19. The correct pair of electrode reactions for electrolysis of aqueous using copper electrodes is:

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20. The balanced anodic half-reaction for acidified-water electrolysis is:

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21. Two standard cells use the half-cell as the cathode. Cell P uses as the anode, while Cell Q uses as the anode. Given , , and , the difference is:

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22. The cathodic half-reaction during electrolysis of molten is:

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23. At , the Nernst equation written with common logarithms is:

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24. Assertion: A weak electrolyte can show a large increase in molar conductivity even though its conductivity decreases on dilution.
Reason: Dilution lowers the number of ions per unit volume but increases ionisation and the conducting contribution per mole.

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25. Consider the following precautions during conductivity measurement.
Statement I: The cell should be rinsed with the solution being measured before the final reading.
Statement II: Air bubbles should not remain attached to the electrode surfaces.
Statement III: The temperature should be kept constant during comparison of solutions.

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26. A rechargeable battery is required for repeated cycling in portable equipment. Compared with a lead storage battery, a nickel-cadmium cell is associated with:

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27. A simplified equation for further oxidation of iron(II) hydroxide during rust formation is:

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28. In an electrochemical cell, an electrode is best described as:

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29. For the Daniell-cell reaction, and at . The equilibrium constant is closest to:

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30. A weak monoprotic acid has concentration and degree of dissociation . Its concentration-form dissociation constant is:

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31. A Daniell cell deposits of copper at the cathode. The amount of zinc consumed at the anode is:

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32. During discharge of a mercury cell, the electrode materials are correctly identified as:

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33. A calculation gives for a weak electrolyte at finite concentration. The safest conclusion is that:

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34. A conductivity cell calibrated at a fixed electrode immersion depth is later used with the electrodes only partly immersed. The original cell constant should not be assumed to remain valid because:

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35. A silver-plating cell deposits of silver in with a current efficiency of . Given and , the current supplied is approximately:

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36. The valid SI-unit combination is:

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37. At , two metal ions compete for reduction at an inert cathode:


If and , which reduction is thermodynamically favoured when kinetic effects are neglected?

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38. Use the standard reduction potentials in the table.

Reduction half-reaction

The strongest oxidising agent and strongest reducing agent among the listed species are respectively:

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39. In the reaction , the reducing agent is:

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40. For a strong electrolyte, at , while at . Assuming linear behaviour, is:

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41. A student claims that a singly charged cation must always be discharged before a doubly charged cation. The most appropriate correction is:

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42. A learner extends a straight line fitted to concentrated strong-electrolyte data and treats the intercept as an exact value of . The main limitation of this method is that:

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43. Two standard half-cells have and . When they form a spontaneous galvanic cell:

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44. Select the correctly written expression for of .

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45. Consider the following statements.
Statement I: Oxidation always occurs at the anode.
Statement II: Reduction always occurs at the cathode.
Statement III: The anode must be negative in every electrochemical cell.

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46. Calibration of a conductivity cell with standard is preferred over calculating only from ruler measurements because:

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47. A student says, “Conductivity must change whenever a solution is transferred to a cell of different dimensions because its measured conductance changes.” The suitable correction is:

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48. For a two-electron reaction at , . Its standard cell potential is:

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49. A calculation for a cell at uses . The main error is that:

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50. An electrode has . At , when , its reduction potential is approximately:

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