1. Complete and Balance the Following Chemical Equations:
(a) Equation:
2MnO₄⁻(aq) + 10I⁻(aq) + 16H⁺(aq) →
Solution:
In acidic medium, MnO₄⁻ gets reduced to Mn²⁺ and I⁻ gets oxidized to I₂.
Half-reactions:
Reduction half-reaction: MnO₄⁻ + 8H⁺ + 5e⁻ → Mn²⁺ + 4H₂O
Oxidation half-reaction: 2I⁻ → I₂ + 2e⁻
Balancing the half-reactions:
Multiply the reduction half-reaction by 2 and the oxidation half-reaction by 5 to equalize the number of electrons transferred.
Reduction: 2MnO₄⁻ + 16H⁺ + 10e⁻ → 2Mn²⁺ + 8H₂O
Oxidation: 10I⁻ → 5I₂ + 10e⁻
Balanced Equation:
2MnO₄⁻(aq) + 10I⁻(aq) + 16H⁺(aq) → 2Mn²⁺(aq) + 5I₂(aq) + 8H₂O(l)
(b) Equation:
Cr₂O₇²⁻(aq) + 6Fe²⁺(aq) + 14H⁺(aq) →
Solution:
In acidic medium, Cr₂O₇²⁻ gets reduced to Cr³⁺ and Fe²⁺ gets oxidized to Fe³⁺.
Half-reactions:
Reduction half-reaction: Cr₂O₇²⁻ + 14H⁺ + 6e⁻ → 2Cr³⁺ + 7H₂O
Oxidation half-reaction: 6Fe²⁺ → 6Fe³⁺ + 6e⁻
Balancing the half-reactions:
The number of electrons is already balanced in the half-reactions.
Balanced Equation:
Cr₂O₇²⁻(aq) + 6Fe²⁺(aq) + 14H⁺(aq) → 2Cr³⁺(aq) + 6Fe³⁺(aq) + 7H₂O(l)
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.