Consider an octahedral complex, \(\mathrm{MA}_{2} \mathrm{~B}_{4}\). How many geometric isomers are expected for this compound? Will any of the isomers be optically active? If so, which ones?

Short Answer

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There are four geometric isomers for the octahedral complex \(\mathrm{MA}_{2}\mathrm{B}_{4}\), with one cis and three trans configurations. Out of these, only one trans isomer (with one A ligand in an axial position and the other in an equatorial position) is optically active, as it lacks a plane of symmetry.

Step by step solution

01

Understanding the structure of an octahedral complex

An octahedral complex has a central metal atom (M) surrounded by six ligands. In this case, we have two ligands of type A and four ligands of type B. To determine the geometric isomers, we need to consider all the possible arrangements for the A and B ligands around the central metal atom.
02

Finding geometric isomers based on ligand positions

To find the geometric isomers, we will consider the following scenarios: 1. Both A ligands are next to each other (cis configuration). 2. Both A ligands are opposite to each other (trans configuration). Here are the possible geometric isomers: - Cis configuration: The two A ligands are adjacent, and the remaining four positions are occupied by B ligands. There is only one way to arrange the ligands in this configuration. - Trans configuration: The two A ligands are opposite each other, and the remaining four positions are occupied by B ligands. In this configuration, we have three possibilities (A ligands in axial position, A ligands in the equatorial position, A ligands in the axial and equatorial position). Hence, we have a total of \(1+3 = 4\) geometric isomers.
03

Identify optically active isomers

An optically active substance has the ability to rotate plane-polarized light. A molecule is optically active if it is not superimposable on its mirror image (i.e., it lacks a plane of symmetry). For the octahedral complex \(\mathrm{MA}_{2}\mathrm{B}_{4}\): - Cis configuration: In this configuration, there is a plane of symmetry passing through the central metal atom and the two A ligands, making it optically inactive. Trans configuration: 1. Both A ligands are in axial positions: This configuration also has a plane of symmetry passing through the axial ligands and perpendicular to the equatorial plane, making this isomer optically inactive. 2. Both A ligands are opposite in the equatorial plane: This configuration has a plane of symmetry passing through the M atom and between A ligands; thus, this isomer is optically inactive. 3. A ligands are in one axial position and one equatorial position such that they are opposite: There is no plane of symmetry in this case, making this isomer optically active. In conclusion, there are four geometric isomers, and only one of them (one trans isomer with A ligands in one axial and one equatorial position) is optically active.

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Most popular questions from this chapter

Indicate the coordination number and the oxidation number of the metal for each of the following complexes: (a) \(\mathrm{Na}_{2}[\mathrm{Co}(\mathrm{EDTA})]\) (b) \(\mathrm{KMnO}_{4}\) (c) \(\left[\mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{4}\right] \mathrm{Cl}_{2}\) (d) \(\mathrm{K}_{3} \mathrm{Fe}(\mathrm{CN})_{6}\) (e) \(\mathrm{Rh}\left(\mathrm{PPh}_{3}\right)_{3} \mathrm{Cl}\) (f) $\mathrm{Zn}\left(\mathrm{C}_{2} \mathrm{O}_{4}\right)\left(\mathrm{NH}_{3}\right)_{2}$

Give the number of (valence) \(d\) electrons associated with the central metal ion in each of the following complexes: (a) $\left[\mathrm{Pt}\left(\mathrm{NH}_{3}\right)_{2} \mathrm{Cl}_{2}\right] \mathrm{Cl}_{2}$, (b) $\mathrm{K}_{2}\left[\mathrm{Cu}\left(\mathrm{C}_{2} \mathrm{O}_{4}\right)_{2}\right]$, (c) \(\left[\mathrm{Os}(\mathrm{en})_{3}\right] \mathrm{Cl}_{3}\), (d) \([\mathrm{Cr}(\mathrm{EDTA})] \mathrm{SO}_{4}\), , (e) $\left[\mathrm{Cd}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right] \mathrm{Cl}_{2}$

Sketch the structure of the complex in each of the following compounds and give the full compound name: (a) $c i s-\left[\operatorname{PtBr} \mathrm{Cl}\left(\mathrm{NO}_{2}\right)_{2}\right]^{2-}$ (b) $\left[\mathrm{Mn}(\mathrm{CO})_{3}\left(\mathrm{C}_{6} \mathrm{H}_{6}\right)\right]^{+}$ (c) $\left.c i s-\left[\mathrm{Cr} \mathrm{Cl}_{4}\right)\left(\mathrm{OH}_{2}\right)_{2}\right]^{-}$ (d) trans-[Co(OH)(en) \(\left._{2} \mathrm{Cl}\right]^{+}\)

Generally speaking, for a given metal and ligand, the stability of a coordination compound is greater for the metal in the +3 rather than in the +2 oxidation state (for metals that form stable +3 ions in the first place). Suggest an explanation, keeping in mind the Lewis acid-base nature of the metal-ligand bond.

Which of the following objects is chiral: \((\mathbf{a})\) a pencil, \((\mathbf{b})\) a computer keyboard, (c) a grand piano, (d) a molecular model of \(c i s-\mathrm{Fe}(\text { bipy })_{2} \mathrm{Cl}_{2},(\mathbf{e})\) a piece of plane \(\mathrm{A} 4\) paper?

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