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Question: For the reaction. \(2AgCl\left( s \right) + {H_2}\left( g \right)\left( {1atm} \right) \to 2Ag\le...

For the reaction.
2AgCl(s)+H2(g)(1atm)2Ag(s)+2H+(0.1M)+2Cl(0.1M)2AgCl\left( s \right) + {H_2}\left( g \right)\left( {1atm} \right) \to 2Ag\left( s \right) + 2{H^ + }\left( {0.1M} \right) + 2C{l^ - }\left( {0.1M} \right)
ΔGo=43600J\Delta {G^o} = - 43600J at 25oC{25^o}C
Calculate the e.m.f of the cell.
[log10n=n]\left[ {\log {{10}^{ - n}} = - n} \right]

Explanation

Solution

Production of AgAg from the AgClAgCl molecules requires a redox reaction to take place. The calculation of e.m.f depends on the value of EcelloE_{cell}^o that needs to be calculated at first and then from there the Ecell{E_{cell}} can be calculated.

Complete step by step answer:
The given reaction of conversion is a redox process where the reduction and oxidation occur based on changes in the oxidation number.
Reduction process is AgCl(s)Ag(s)AgCl\left( s \right) \to Ag(s)
Oxidation process is H2(g)2H+{H_2}\left( g \right) \to 2{H^ + }
These are the two processes taking place in the reaction and hence based on this process EcelloE_{cell}^o can be calculated using the given calculated values. Here F=96500F = 96500 which is the Faraday’s constant and nn is the number of molecules that are involved in the reaction.
Ecello=GnFE_{cell}^o = \dfrac{G}{{nF}}
Putting the values in the equation we get,
Ecello=(43600)2×96500E_{cell}^o = \dfrac{{ - ( - 43600)}}{{2 \times 96500}}
Ecello=0.23\Rightarrow E_{cell}^o = 0.23
Therefore, now the EcelloE_{cell}^o is calculated and from there the Ecell{E_{cell}} can be easily calculated. Based on this calculation the e.m.f of the cell can be formulated. The products are taken as the numerator using the 22 molecules of each as the power of each.
Ecell=Ecello0.0591nlog[H+]2[Cl]21{E_{cell}} = E_{cell}^o - \dfrac{{0.0591}}{n}\log \dfrac{{{{\left[ {{H^ + }} \right]}^2}{{\left[ {C{l^ - }} \right]}^2}}}{1}
Taking molarity values as concentration Ecell=0.230.05912log(110)2(110)2 \Rightarrow {E_{cell}} = 0.23 - \dfrac{{0.0591}}{2}\log {\left( {\dfrac{1}{{10}}} \right)^2}{\left( {\dfrac{1}{{10}}} \right)^2}
Ecell=0.230.05912log(101)4\Rightarrow {E_{cell}} = 0.23 - \dfrac{{0.0591}}{2}\log {\left( {{{10}^{ - 1}}} \right)^4}
Ecell=0.230.05912log(104)\Rightarrow {E_{cell}} = 0.23 - \dfrac{{0.0591}}{2}\log \left( {{{10}^{ - 4}}} \right)
Since it is already given before that, [log10n=n]\left[ {\log {{10}^{ - n}} = - n} \right]
Hence Ecell=0.230.05912×(4) \Rightarrow {E_{cell}} = 0.23 - \dfrac{{0.0591}}{2} \times \left( { - 4} \right)
\Rightarrow {E_{cell}} = 0.23 - \left\\{ {0.0591 \times \left( { - 2} \right)} \right\\}
Ecell=0.23+0.1182\Rightarrow {E_{cell}} = 0.23 + 0.1182
Ecell=0.3482\Rightarrow {E_{cell}} = 0.3482

Therefore the e.m.f. of the cell for the given set of conditions is 0.34820.3482. This is the value of the emf of the specific cell under the condition where AgClAgCl is converted to AgAg. Therefore, formulating the redox reaction is important in the process so that EcelloE_{cell}^o can be calculated as the oxidation half cell and reduction half cell of the process can be easily formulated.

Note: Calculating the emf of a cell requires the calculation of EcelloE_{cell}^o which includes the difference between the Eo{E^o} at the cathode and Eo{E^o} at the anode of the cell. This shows the e.m.f of the electrophoretic cell which makes the change from the AgClAgCl to AgAg during the process.