(i) Ambidentate ligand, restated:
Step 1: Recall that a ligand donates a lone pair to the metal. Some anions carry lone pairs on two chemically different atoms. Such a ligand can attach through atom A in one complex and through atom B in another; this switchable behaviour is called ambidentate character (from Latin ambi = both).
Step 2: Quick examples with the linkage isomers they produce: SCN- (S-bonded thiocyanato vs N-bonded isothiocyanato), NO2- (N-bonded nitro vs O-bonded nitrito), and CN- (C-bonded cyano vs N-bonded isocyano). This is the origin of linkage isomerism.
(ii) Naming by a fixed procedure. Order of writing a coordination name: number-prefix + ligands in alphabetical order + metal (with -ate suffix if the ion is an anion) + oxidation state in Roman numerals; for salts the counter-ion is written first.
a) Deduce the metal charge from the +1 overall charge: neutral en contributes 0, two Br- contribute -2, so metal \(= +1 - (-2) = +3\). Apply the procedure: dibromido, then bis(ethane-1,2-diamine), then cobalt(III).
Answer: Dibromidobis(ethane-1,2-diamine)cobalt(III) ion.
b) Potassium is the counter-cation, so name it first. The anion has charge -3 (balancing three K+); with three oxalate (-2 each = -6), the metal is \(-3 + 6 = +3\). Because the complex is an anion, iron becomes ferrate; three chelating oxalate groups take tris.
Answer: Potassium tris(oxalato)ferrate(III).