The given name is Tetraamminedibromoplatinum(IV) bromide.
Step 1: Identify the ligands and metal oxidation state.
- “Tetraammine” → 4 \( \text{NH}_3 \) ligands (neutral).
- “Dibromo” → 2 \( \text{Br}^- \) ligands (inside the coordination sphere).
- “Platinum(IV)” → Metal oxidation state = +4.
- “Bromide” (at the end of the name) → counter anion(s) outside the coordination sphere.
Step 2: Write the partial complex formula: \[ [\text{PtBr}_2(\text{NH}_3)_4]^{?} \]
Step 3: Determine the charge on the complex ion. Let the overall charge on the coordination sphere be \( x \). \[ x + (2 \times -1) + (4 \times 0) = +4 \] \[ x - 2 = +4 \implies x = +6 \] This would be incorrect since Pt(IV) rarely forms +6 complexes. Let’s reconsider the ligand count relative to oxidation state.
In the complex \( [\text{PtBr}_2(\text{NH}_3)_4] \), platinum has oxidation number: \[ x + (2 \times -1) = +4 \implies x = +6 \] Wait — correction: for a **Pt(IV)** ion, the total oxidation number is +4. So, \[ +4 = x + (-2) \implies x = +6 \] That means two bromides inside (each -1) give the total +4 charge for platinum. The coordination sphere has a net charge of +2.
Therefore, to balance the charge, there must be **two bromide ions** outside the coordination sphere. \[ [\text{PtBr}_2(\text{NH}_3)_4]\text{Br}_2 \]
Hence, the correct formula is: \[ \boxed{[\text{PtBr}_2(\text{NH}_3)_4]\text{Br}_2} \]
(i) Draw the diagram which indicates the splitting of d-orbitals in tetrahedral field.
(ii) Write any one limitation of valence bond theory.
(i)[Ni(CN)₄]²⁻ and [Ni(CO)(_4)] have different structures, but do not differ in their magnetic behaviour. Explain.
(ii) Write the formula of Tetraamineaquachloridocobalt(III)chloride.
(i) Write two postulates of Werner's coordination theory.
(ii) Draw the geometrical isomers of [(NH_3)_3(NO_2)_3] and give their structures.