Step 1: Understanding Inner and Outer Orbital Complexes. Inner orbital complexes involve the use of \( d \)-orbitals from the inner shell (typically the \( 3d \)-orbitals in transition metals). This type of hybridization leads to low-spin complexes, where ligands coordinate using these inner \( d \)-orbitals.
Outer orbital complexes involve the use of \( d \)-orbitals from the outer shell (typically \( 4d \)-orbitals for transition metals in higher oxidation states). This type of hybridization leads to high-spin complexes, where ligands coordinate using these outer \( d \)-orbitals.
Step 2: Identifying the Hybridization in \( [Co(NH_3)_6]^{3+ \).} Cobalt in the \( +3 \) oxidation state has an electronic configuration of \( 3d^6 \), and the complex \( [Co(NH_3)_6]^{3+} \) uses inner \( 3d \)-orbitals for bonding with the ligands. The \( 3d^2sp^3 \) hybridization results in an inner orbital complex.
Step 3: Identifying the Hybridization in \( [Ni(NH_3)_6]^{2+ \).} Nickel in the \( +2 \) oxidation state has an electronic configuration of \( 3d^8 \), and the complex \( [Ni(NH_3)_6]^{2+} \) uses outer \( 4d \)-orbitals for bonding. The \( sp^3d^2 \) hybridization results in an outer orbital complex. Thus, \( [Co(NH_3)_6]^{3+} \) is an inner orbital complex, while \( [Ni(NH_3)_6]^{2+} \) is an outer orbital complex.
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.