To solve the problem, we need to calculate the cell potential of the electrochemical cell formed by connecting the Sn$^{4+}$/Sn$^{2+}$ and Cr$^{3+}$/Cr couples in their standard states.
1. Understanding the Standard Electrode Potentials:
The standard electrode potential (E°) for the two couples is given as:
The cell potential (E°cell) is calculated by taking the difference between the electrode potentials of the two half-reactions. The couple with the more positive potential will undergo reduction, while the other will undergo oxidation.
2. Identifying the Anode and Cathode:
In this case: - Sn$^{4+}$ will be reduced to Sn$^{2+}$ because it has the more positive electrode potential (+0.15 V), so it will act as the cathode. - Cr will be oxidized to Cr$^{3+}$ because it has the more negative electrode potential (-0.74 V), so it will act as the anode.
3. Calculating the Cell Potential:
The cell potential (E°cell) is given by the equation: E°cell = E°(cathode) - E°(anode)
Substituting the values: E°cell = (+0.15 V) - (-0.74 V)E°cell = 0.15 V + 0.74 V = 0.89 V
Final Answer:
The cell potential will be 0.89 V.
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.