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Question: From the following information, AgBr(s) + e → Ag(s) + Bre(aq); E° = 0.09 V Ag⊕(aq) + e → Ag(s); E° ...

From the following information,

AgBr(s) + e → Ag(s) + Bre(aq); E° = 0.09 V Ag⊕(aq) + e → Ag(s); E° = 0.81 V If the solubility product of AgBr is 1x10⁻ˣ, then x is

(Given,2.303RTF=0.06)\qquad \Bigg( Given, \frac{2.303 RT}{F} = 0.06 \Bigg)

Answer

12

Explanation

Solution

To determine the solubility product (KspK_{sp}) of AgBr, we need to relate the given standard electrode potentials to the equilibrium reaction for AgBr dissolution.

The solubility product of AgBr is defined by the equilibrium: AgBr(s)Ag+(aq)+Br(aq)AgBr(s) \rightleftharpoons Ag^+(aq) + Br^-(aq) Ksp=[Ag+][Br]K_{sp} = [Ag^+][Br^-]

We are given two standard electrode potentials:

  1. AgBr(s)+eAg(s)+Br(aq)AgBr(s) + e^- \rightarrow Ag(s) + Br^-(aq); E1=0.09VE^\circ_1 = 0.09 V
  2. Ag+(aq)+eAg(s)Ag^+(aq) + e^- \rightarrow Ag(s); E2=0.81VE^\circ_2 = 0.81 V

To obtain the reaction AgBr(s)Ag+(aq)+Br(aq)AgBr(s) \rightleftharpoons Ag^+(aq) + Br^-(aq), we can subtract the first half-reaction from the second half-reaction: (Ag+(aq)+eAg(s))(AgBr(s)+eAg(s)+Br(aq))(Ag^+(aq) + e^- \rightarrow Ag(s)) - (AgBr(s) + e^- \rightarrow Ag(s) + Br^-(aq)) This yields: Ag+(aq)AgBr(s)Br(aq)Ag^+(aq) - AgBr(s) \rightarrow -Br^-(aq) Rearranging, we get the reaction: Ag+(aq)+Br(aq)AgBr(s)Ag^+(aq) + Br^-(aq) \rightarrow AgBr(s)

The standard cell potential (ErxnE^\circ_{rxn}) for this reaction is the difference between the standard electrode potentials of the two half-reactions: Erxn=E2E1=0.81V0.09V=0.72VE^\circ_{rxn} = E^\circ_2 - E^\circ_1 = 0.81 V - 0.09 V = 0.72 V

The equilibrium constant for the reaction Ag+(aq)+Br(aq)AgBr(s)Ag^+(aq) + Br^-(aq) \rightarrow AgBr(s) is K=1[Ag+][Br]=1KspK = \frac{1}{[Ag^+][Br^-]} = \frac{1}{K_{sp}}.

Now, we use the relationship between the standard cell potential and the equilibrium constant, which is derived from the Nernst equation: Erxn=2.303RTnFlogKE^\circ_{rxn} = \frac{2.303 RT}{nF} \log K Given 2.303RTF=0.06V\frac{2.303 RT}{F} = 0.06 V. The number of electrons transferred (nn) for this reaction is 1 (as seen from the half-reactions).

Substitute the values into the equation: 0.72V=0.061log(1Ksp)0.72 V = \frac{0.06}{1} \log \left(\frac{1}{K_{sp}}\right) 0.72=0.06(logKsp)0.72 = 0.06 (-\log K_{sp}) Divide both sides by 0.06: logKsp=0.720.06-\log K_{sp} = \frac{0.72}{0.06} logKsp=12-\log K_{sp} = 12 logKsp=12\log K_{sp} = -12

To find KspK_{sp}, take the antilog: Ksp=1012K_{sp} = 10^{-12}

The problem states that the solubility product of AgBr is 1×10x1 \times 10^{-x}. Comparing our calculated KspK_{sp} with the given form: 1×10x=1×10121 \times 10^{-x} = 1 \times 10^{-12} Therefore, x=12x = 12.