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The electrochemical cell shown below is a concentration cell.
M|M2+ (saturated solut ion of a sparingly so luble salt, MX2 || M2+ (0.001 mol dm–3)| M.
The emf of the cell depends on the difference in concentration of M2+ ions at the two electrodes. The emf of the cell at 298  is 0.059 V.
Q. 
The solubility product (Ksp ; mol3 dm–9) of MX2 at 298 based on the informat ion available the given concentration cell is (take 2.303 × R × 298/F = 0.059 V)
  • a)
    1 × 10–15
  • b)
    4 × 10–15
  • c)
    1 × 10–12
  • d)
    4 × 10–12
Correct answer is option 'B'. Can you explain this answer?
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The electrochemical cell shown below is a concentration cell.M|M2+ (sa...
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The electrochemical cell shown below is a concentration cell.M|M2+ (sa...
Given information:
- Electrochemical cell is a concentration cell.
- Half-cell reactions: M+ + e- → M (saturated solution of a sparingly soluble salt, MX2)
M2+ + 2e- → M (0.001 mol dm-3)
- EMF of the cell at 298K = 0.059 V
- 2.303RT/F = 0.059 V (at 298K)

To find: Solubility product (Ksp) of MX2 at 298K

Solution:
The given cell is a concentration cell, which means that the two half-cells have the same electrode but different concentrations of M2+ ions. The concentration of M2+ ions at the two electrodes can be related to the solubility product of MX2 using the Nernst equation:

Ecell = E°cell - (RT/nF) ln Q

where Ecell is the cell potential, E°cell is the standard cell potential, R is the gas constant, T is the temperature, n is the number of electrons transferred in the cell reaction, F is the Faraday constant, and Q is the reaction quotient.

For the given cell, the half-cell reactions and their standard reduction potentials are:

M+ + e- → M (saturated solution of a sparingly soluble salt, MX2) E°1 = ?

M2+ + 2e- → M E°2 = E°°M2+/M - E°°M

The standard potential of the M2+/M half-reaction can be calculated using the Nernst equation:

E°°M2+/M = (RT/nF) ln(Ksp)

where Ksp is the solubility product of MX2.

Substituting the given values into the Nernst equation for the cell:

0.059 V = E°1 - (RT/nF) ln(Q)

where Q = [M2+] / [M+] (the concentration of M+ ions is assumed to be constant and equal to the saturation concentration)

Taking the antilog of both sides:

Q = [M2+] / [M+] = e^(nF(E°1 - 0.059 V) / RT)

Substituting the standard potential of the M2+/M half-reaction and rearranging:

Ksp = [M2+]^2 [M+]^-1 = e^(2nF(E°1 - 0.059 V) / RT)

Using the value of 2.303RT/F = 0.059 V at 298K and n = 2 (since two electrons are transferred in the cell reaction):

Ksp = e^(4.605(E°1 - 0.059) / 0.059) = e^(78.0508E°1 - 78.0508)

Taking the antilog of both sides:

Ksp = 10^(78.0508E°1 - 78.0508)

To find the value of E°1, we can use the standard potentials of the half-reactions for M and M2+ ions:

E°1 = E°°M - E°°M2+/M = E°°M - (RT/2F) ln([M2+]/[M])

Substituting the given values:

E°1 = -0.059 - (
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The electrochemical cell shown below is a concentration cell.M|M2+ (saturated solut ion of a sparingly so luble salt, MX2 || M2+ (0.001 mol dm–3)| M.The emf of the cell depends on the difference in concentration of M2+ ions at the two electrodes. The emf of the cell at 298 is 0.059 V.Q.The solubility product (Ksp ; mol3 dm–9) of MX2 at 298 based on the informat ion available the given concentration cell is (take 2.303 × R × 298/F = 0.059 V)a)1 × 10–15b)4 × 10–15c)1 × 10–12d)4 × 10–12Correct answer is option 'B'. Can you explain this answer?
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