Draw the \(d\) -orbital splitting diagrams for the octahedral complex ions of each of the following. a. \(\mathrm{Zn}^{2+}\) b. \(\mathrm{Co}^{2+}\) (high and low spin) c. \(\mathrm{Ti}^{3+}\)

Short Answer

Expert verified
The d-orbital splitting diagrams for the octahedral complex ions are as follows: a. Zn²⁺: No splitting occurs as all d-orbitals are completely filled (d¹⁰ configuration). b. Co²⁺: - High spin: 4 orbitals with one electron and 1 orbital with two electrons. - Low spin: 3 orbitals with one electron and 1 orbital with three electrons. c. Ti³⁺: One electron in the lowest energy d-orbital and four empty d-orbitals.

Step by step solution

01

a. Zn²⁺ d-orbital Splitting Diagram

Step 1: Determine the electron configuration of Zn²⁺. Zinc has an atomic number of 30, so its ground state electron configuration is \[1s^2 2s^2 2p^6 3s^2 3p^6 3d^{10} 4s^2\] In the Zn²⁺ ion, it loses two electrons from the 4s orbital: \[1s^2 2s^2 2p^6 3s^2 3p^6 3d^{10}\] Step 2: Draw the d-orbital splitting diagram. Zn²⁺ ion is a d¹⁰ metal, meaning that all five d-orbitals are completely filled. Since there is no interaction between the d-electrons and ligands, there is no splitting in the Zn²⁺ d-orbitals.
02

b. Co²⁺ (High and Low Spin) d-Orbital Splitting Diagram

Step 1: Determine the electron configuration of Co²⁺. Cobalt has an atomic number of 27, so its ground state electron configuration is \[1s^2 2s^2 2p^6 3s^2 3p^6 3d^7 4s^2\] In the Co²⁺ ion, it loses two electrons, one from the 4s and one from the 3d orbital: \[1s^2 2s^2 2p^6 3s^2 3p^6 3d^6\] Step 2: Draw the d-orbital splitting diagram for high spin. In a high-spin complex, the crystal field splitting energy (Δ) is small, and the electrons will fill all five d-orbitals before any of the orbitals are doubly occupied. The diagram will show 4 orbitals with one electron and 1 orbital with two electrons. Step 3: Draw the d-orbital splitting diagram for low spin. In a low-spin complex, the crystal field splitting energy (Δ) is large, and the electrons will first completely fill the lower energy d-orbitals before moving to the higher energy orbitals. The diagram will show 3 orbitals with one electron and 1 orbital with three electrons.
03

c. Ti³⁺ d-Orbital Splitting Diagram

Step 1: Determine the electron configuration of Ti³⁺. Titanium has an atomic number of 22, so its ground state electron configuration is \[1s^2 2s^2 2p^6 3s^2 3p^6 3d^2 4s^2\] In the Ti³⁺ ion, it loses two electrons from the 4s and one from the 3d orbital: \[1s^2 2s^2 2p^6 3s^2 3p^6 3d^1\] Step 2: Draw the d-orbital splitting diagram for Ti³⁺. The Ti³⁺ ion is a d¹ metal, meaning it has only one unpaired electron in its d-orbitals. The octahedral splitting diagram will show one electron in the lowest energy d-orbital, and the other four orbitals will be empty.

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Most popular questions from this chapter

Ammonia and potassium iodide solutions are added to an aqueous solution of \(\mathrm{Cr}\left(\mathrm{NO}_{3}\right)_{3} .\) A solid is isolated (compound \(\mathrm{A}\) ), and the following data are collected: i. When \(0.105 \mathrm{~g}\) of compound \(\mathrm{A}\) was strongly heated in excess \(\mathrm{O}_{2}, 0.0203 \mathrm{~g} \mathrm{CrO}_{3}\) was formed. ii. In a second experiment it took \(32.93 \mathrm{~mL}\) of \(0.100 \mathrm{M} \mathrm{HCl}\) to titrate completely the \(\mathrm{NH}_{3}\) present in \(0.341 \mathrm{~g}\) compound \(\mathrm{A}\). iii. Compound A was found to contain \(73.53 \%\) iodine by mass. iv. The freezing point of water was lowered by \(0.64^{\circ} \mathrm{C}\) when \(0.601\) g compound \(A\) was dissolved in \(10.00 \mathrm{~g} \mathrm{H}_{2} \mathrm{O}\) \(\left(K_{\mathrm{f}}=1.86^{\circ} \mathrm{C} \cdot \mathrm{kg} / \mathrm{mol}\right)\) What is the formula of the compound? What is the structure of the complex ion present? (Hints: \(\mathrm{Cr}^{3+}\) is expected to be sixcoordinate, with \(\mathrm{NH}_{3}\) and possibly \(\mathrm{I}^{-}\) as ligands. The \(\mathrm{I}^{-}\) ions will be the counterions if needed.)

What is the lanthanide contraction? How does the lanthanide contraction affect the properties of the \(4 d\) and \(5 d\) transition metals?

A certain first-row transition metal ion forms many different colored solutions. When four coordination compounds of this metal, each having the same coordination number, are dissolved in wa ter, the colors of the solutions are red, yellow, green, and blue Further experiments reveal that two of the complex ions are para magnetic with four unpaired electrons and the other two are dia magnetic. What can be deduced from this information about th four coordination compounds?

Use standard reduction potentials to calculate \(\mathscr{E}^{\circ}, \Delta G^{\circ}\), and \(K\) (at \(298 \mathrm{~K}\) ) for the reaction that is used in production of gold: $$2 \mathrm{Au}(\mathrm{CN})_{2}^{-}(a q)+\mathrm{Zn}(s) \longrightarrow 2 \mathrm{Au}(s)+\mathrm{Zn}(\mathrm{CN})_{4}^{2-}(a q)$$ The relevant half-reactions are $$\begin{aligned}\mathrm{Au}(\mathrm{CN})_{2}^{-}+\mathrm{e}^{-} \longrightarrow \mathrm{Au}+2 \mathrm{CN}^{-} & \mathscr{C}^{\circ} &=-0.60 \mathrm{~V} \\ \mathrm{Zn}(\mathrm{CN})_{4}^{2-}+2 \mathrm{e}^{-} \longrightarrow \mathrm{Zn}+4 \mathrm{CN}^{-} & \mathscr{E}^{\circ} &=-1.26 \mathrm{~V} \end{aligned}$$

How many unpaired electrons are present in the tetrahedral ion \(\mathrm{FeCl}_{4}^{-} ?\)

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