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.
Write IUPAC names of the following compounds and classify them into primary, secondary and tertiary amines.
(i) (CH3 )2CHNH2 (ii) CH3 (CH2 )2NH2 (iii) CH3NHCH(CH3 )2
(iv) (CH3 )3CNH2 (v) C6H5NHCH3 (vi) (CH3CH2 )2NCH3 (vii) m–BrC6H4NH2
Give one chemical test to distinguish between the following pairs of compounds.
(i) Methylamine and dimethylamine
(ii) Secondary and tertiary amines
(iii) Ethylamine and aniline
(iv) Aniline and benzylamine
(v) Aniline and N-methylaniline
Account for the following:
(i) pKb of aniline is more than that of methylamine.
(ii) Ethylamine is soluble in water whereas aniline is not.
(iii) Methylamine in water reacts with ferric chloride to precipitate hydrated ferric oxide.
(iv) Although amino group is o– and p– directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of m-nitroaniline.
(v) Aniline does not undergo Friedel-Crafts reaction.
(vi) Diazonium salts of aromatic amines are more stable than those of aliphatic amines. (vii) Gabriel phthalimide synthesis is preferred for synthesising primary amines.
\(FeSO_4\) solution mixed with\( (NH_4)_2SO_4 \) solution in\( 1:1\) molar ratio gives the test of \(Fe^{2+}\) ion but \(CuSO_4\) solution mixed with aqueous ammonia in \( 1:4 \) molar ratio does not give the test of \(Cu^{2+}\) ion. Explain why?
Specify the oxidation numbers of the metals in the following coordination entities:
(i)\( [Co(H_2O)(CN)(en)_2] ^{2+}\)
(ii) \([CoBr_2(en)_2]^{+}\)
(iii)\( [PtCl_4]^{ 2–} \)
(iv) \(K_3[Fe(CN)_6]\)
(v) \([Cr(NH_3)_3Cl_3] \)