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Question: From the following information, calculate the solubility product of \[AgBr\] . \[AgB{r_{(s)}} + {e...

From the following information, calculate the solubility product of AgBrAgBr .
AgBr(s)+eAg(s)+Br(aq):Eo=0.07VAgB{r_{(s)}} + {e^ - } \to A{g_{(s)}} + B{r^ - }_{(aq)}:{E^o} = 0.07V
Ag+(aq)+eAg(s):Eo=0.80VA{g^ + }_{(aq)} + {e^ - } \to A{g_{(s)}}:{E^o} = 0.80V
A. 4×10134 \times {10^{ - 13}}
B. 4×10104 \times {10^{ - 10}}
C. 4×10174 \times {10^{ - 17}}
D. 4×1074 \times {10^{ - 7}}

Explanation

Solution

We need to remember that the solubility product constant will explain the saturated solution of ionic compounds in a solution or it can be the equilibrium constant for the dissolution of a solid substance into aqueous solution. It is denoted as Ksp{K_{sp}} . Now, let us know about electrode potential. It can also be termed as oxidation electrode potential or reduction electrode potential depending upon the reaction undergone by the electrode if loss of electron (oxidation) takes place at the electrode termed as oxidation potential. If the electrons have the tendency to gain electrons then it is called as reduction electrode potential. It is measured in volts (V) or millivolts (mV).

Complete step by step answer:
We can write the dissolution of AgBrAgBr in cell will be,
In anode Ag(s)+Br(aq)AgBr(s)A{g_{(s)}} + B{r^ - }_{(aq)} \to AgB{r_{(s)}}
In cathode Ag+(aq)+eAg(s)A{g^ + }_{(aq)} + {e^ - } \to A{g_{(s)}}
Overall reaction Ag+(aq)+Br(aq)AgBr(s)A{g^ + }_{(aq)} + B{r^ - }_{(aq)} \to AgB{r_{(s)}}
In AgBrAgBr , cell potential of a cell (Ecell)=0\left( {{E_{cell}}} \right) = 0
Given the standard potential (E0)\left( {{E^0}} \right) of cathode is 0.07V0.07V and the standard potential (E0E^0) of anode is 0.08V0.08V .Then the total cell electrode potential Ecell0E_{cell}^0 can be calculated by
Ecell0=Ecathode0Eanode0E_{cell}^0 = E_{cathode}^0 - E_{anode}^0
Now apply the E0 values in the above equation,
E0cell=0.80V0.07V{E^0}_{cell} = 0.80V - 0.07V
The total cell electrode potential,E0cell=0.73V{E^0}_{cell} = 0.73V
From electrode potential we can calculate KSP{K_{SP}} by the formula
Ecell=E00.059nlogKSP{E_{cell}} = {E^0} - \dfrac{{0.059}}{n}\log {K_{SP}}
n= number of moles of electrons transferred
From the above reaction , n=1
Since it is equilibrium reaction Ecell=0{E_{cell}} = 0
0=0.730.0591logKsp0 = 0.73 - \dfrac{{0.059}}{1}\log {K_{sp}}
Now bring the total cell electrode potential value i.e) 0.73 to the left hand side,
0.73=0.0591logKsp0.73 = - \dfrac{{0.059}}{1}\log {K_{sp}}
Now let us keep logKsplog{K_{sp}} on one side and values on the other side like
logKSP =(0.73)10.059log{K_{SP}}{\text{ }} = - \left( {0.73} \right)\dfrac{1}{{0.059}}
By solving the above step,
logKSP=12.37log{K_{SP}} = - 12.37
Now to find the value ofKsp{K_{sp}} , bring log to the right hand side log becomes antilog,
Ksp=antilog(12.37){K_{sp}} = anti\log ( - 12.37)
Then the value is, KSP=4×1013{K_{SP}} = 4 \times {10^{ - 13}}

So, the correct answer is Option A.

Note: We have to remember that at equilibrium condition cell potential is equal to zero. Under standard conditions, the standard electrode potential occurs in an electrochemical cell say the temperature = 298K, pressure = 1atm, concentration = 1M.solubility product can be calculated directly from the molarity or by concentration of the products i.e) it is product of concentration of the product of the reaction.