Write two consequences of lanthanide contraction.
To solve the problem, we need to identify two consequences of lanthanide contraction.
1. Understand Lanthanide Contraction:
Lanthanide contraction refers to the gradual decrease in ionic radii of lanthanide elements (from La to Lu) due to poor shielding by the 4f electrons, leading to a stronger nuclear attraction on the outer electrons.
2. Consequence 1 - Similarity in Properties of Post-Lanthanide Elements:
Due to lanthanide contraction, the ionic radii of 4d and 5d transition elements (e.g., Zr and Hf) are very similar. This leads to similar chemical properties, making their separation difficult.
3. Consequence 2 - Basicity of Lanthanide Hydroxides:
Lanthanide contraction causes a decrease in ionic size across the series, increasing the charge density of \( Ln^{3+} \) ions. This enhances the polarizing power, reducing the basicity of hydroxides (\( Ln(OH)_3 \)) from La to Lu.
Final Answer:
Two consequences of lanthanide contraction are: (1) Similar ionic radii and chemical properties of 4d and 5d transition elements (e.g., Zr and Hf), making separation challenging. (2) Decrease in basicity of lanthanide hydroxides (\( Ln(OH)_3 \)) across the series due to increasing charge density of \( Ln^{3+} \).
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.
Which is the correct IUPAC name for
