To solve the problem, we need to calculate the potential for a half-cell containing the following concentrations: 0.01 M K₂Cr₂O₇ (aq), 0.01 M Cr³⁺ (aq), and 1.0 × 10⁻⁴ M H⁺ (aq).
1. Understanding the Reaction and Nernst Equation:
We are given a half-cell containing a redox couple involving Cr₂O₇²⁻ (dichromate) and Cr³⁺ (chromium ion). The half-reaction for this system is:
\[ \text{Cr}_2\text{O}_7^{2-}(aq) + 14H^+(aq) + 6e^- \rightarrow 2\text{Cr}^{3+}(aq) + 7H_2O(l) \]
To calculate the potential, we can use the Nernst equation:
\[ E = E^\circ - \frac{0.0591}{n} \log Q \]
where:
- \( E^\circ \) is the standard electrode potential for the half-reaction,
- \( n \) is the number of electrons transferred,
- \( Q \) is the reaction quotient, which is the ratio of concentrations of products to reactants.
2. Standard Electrode Potential:
The standard electrode potential for the half-reaction is given as:
\[ E^\circ = +1.33 \, \text{V} \]
3. Reaction Quotient (Q):
The reaction quotient \( Q \) is given by the expression:
\[ Q = \frac{[\text{Cr}^{3+}]^2 [\text{H}_2\text{O}]^7}{[\text{Cr}_2\text{O}_7^{2-}] [\text{H}^+]^{14}} \]
However, since water (\( \text{H}_2\text{O} \)) is a pure liquid, its concentration is considered constant and does not appear in the expression for \( Q \). Therefore, we have:
\[ Q = \frac{[\text{Cr}^{3+}]^2}{[\text{Cr}_2\text{O}_7^{2-}] [\text{H}^+]^{14}} \]
4. Substituting the Concentrations:
We are given:
- \( [\text{Cr}_2\text{O}_7^{2-}] = 0.01 \, \text{M} \)
- \( [\text{Cr}^{3+}] = 0.01 \, \text{M} \)
- \( [\text{H}^+] = 1.0 \times 10^{-4} \, \text{M} \)
Substituting these values into the expression for \( Q \), we get:
\[ Q = \frac{(0.01)^2}{(0.01)(1.0 \times 10^{-4})^{14}} \]
5. Nernst Equation Calculation:
Now, we substitute the values into the Nernst equation:
\[ E = 1.33 - \frac{0.0591}{6} \log Q \]
Calculating the value of \( Q \) and then applying the Nernst equation will give us the potential for the half-cell under the given conditions.
Final Answer:
We can calculate \( E \) using these equations and constants to find the potential of the half-cell.
The Crystal Field Theory (CFT) of coordination compounds is based on the effect of different crystal fields (provided by the ligands taken as point charges) on the degeneracy of d-orbital energies of the central metal atom/ion. The splitting of the d-orbitals provides different electronic arrangements in strong and weak crystal fields. In tetrahedral coordination entity formation, the d-orbital splitting is smaller as compared to the octahedral entity.
What is crystal field splitting energy?
The Crystal Field Theory (CFT) of coordination compounds is based on the effect of different crystal fields (provided by the ligands taken as point charges) on the degeneracy of d-orbital energies of the central metal atom/ion. The splitting of the d-orbitals provides different electronic arrangements in strong and weak crystal fields. In tetrahedral coordination entity formation, the d-orbital splitting is smaller as compared to the octahedral entity.
On the basis of CFT, explain why [Ti(H$_2$O)$_6$]Cl$_3$ complex is coloured? What happens on heating the complex [Ti(H$_2$O)$_6$]Cl$_3$? Give reason.