The cell potential \(E_{\text{cell}}\) is given as 0.43 V. For the cell: \(Cu(s)|Cu^{2+}(0.001M)||Ag^+(0.01M)|Ag(s)\), we write the reaction as:
\(Cu(s) + 2Ag^+(0.01M) \rightarrow Cu^{2+}(0.001M) + 2Ag(s)\).
Given \(E_{Ag^+/Ag^⊖}=0.80\) V, we apply the Nernst equation:
\(E_{\text{cell}} = E^\circ_{\text{cell}} - \frac{0.06}{2} \log \frac{[Cu^{2+}]}{[Ag^+]^2}\)
Substitute known values:
\(0.43 = E^\circ_{\text{cell}} - \frac{0.03}{2} \log \frac{0.001}{(0.01)^2}\)
\(0.43 = E^\circ_{\text{cell}} - 0.03 \log 10^3\)
\(0.43 = E^\circ_{\text{cell}} - 0.03 \times 3\)
\(0.43 = E^\circ_{\text{cell}} - 0.09\)
\(E^\circ_{\text{cell}} = 0.52\) V
For the standard cell potential: \(E^\circ_{\text{cell}} = E^\circ_{Ag^+/Ag} - E^\circ_{Cu^{2+}/Cu}\),
we find \(E^\circ_{Cu^{2+}/Cu}\):
\(0.52 = 0.80 - E^\circ_{Cu^{2+}/Cu}\)
\(E^\circ_{Cu^{2+}/Cu} = 0.80 - 0.52 = 0.28\) V
The magnitude is \(28 \times 10^{-2}\) V, which fits within the given range of 34,34.
\(E=E^∘–\frac {0.06}{2}log\frac {[Cu^{2+}]}{[Ag^⊕]^2}\)
\(E=E^∘–\frac {0.06}{2}log\frac {0.001}{(0.01)^2}\)
\(0.43=E^∘–0.03\)
\(E^∘=0.46 V\)
\(E^∘_{Ag^⊕/Ag}−E^∘_{Cu^{2+}{Cu}}=0.46\)
\(∴E^∘_{Cu^{2+}{Cu}}=0.8–0.46\)
= \(0.34 V\)
\(= 34 × 10^{-2}V\)
So, the answer is \(34\).
Calculate the EMF of the Galvanic cell: $ \text{Zn} | \text{Zn}^{2+}(1.0 M) \parallel \text{Cu}^{2+}(0.5 M) | \text{Cu} $ Given: $ E^\circ_{\text{Zn}^{2+}/\text{Zn}} = -0.763 \, \text{V} $ and $ E^\circ_{\text{Cu}^{2+}/\text{Cu}} = +0.350 \, \text{V} $
A substance 'X' (1.5 g) dissolved in 150 g of a solvent 'Y' (molar mass = 300 g mol$^{-1}$) led to an elevation of the boiling point by 0.5 K. The relative lowering in the vapour pressure of the solvent 'Y' is $____________ \(\times 10^{-2}\). (nearest integer)
[Given : $K_{b}$ of the solvent = 5.0 K kg mol$^{-1}$]
Assume the solution to be dilute and no association or dissociation of X takes place in solution.
Galvanic cells, also known as voltaic cells, are electrochemical cells in which spontaneous oxidation-reduction reactions produce electrical energy. It converts chemical energy to electrical energy.
It consists of two half cells and in each half cell, a suitable electrode is immersed. The two half cells are connected through a salt bridge. The need for the salt bridge is to keep the oxidation and reduction processes running simultaneously. Without it, the electrons liberated at the anode would get attracted to the cathode thereby stopping the reaction on the whole.