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Determine if each of the following metal complexes is chiral and therefore has an optical isomer: (a) square planar \(\left[\mathrm{Pd}(\mathrm{en})(\mathrm{CN})_{2}\right],(\mathbf{b})\) octahedral \(\left[\mathrm{Ni}(\mathrm{en})\left(\mathrm{NH}_{3}\right)_{4}\right]^{2+},(\mathbf{c})\) octahe- dral \(\operatorname{cis}-\left[\mathrm{V}(\mathrm{en})_{2} \mathrm{ClBr}\right]\)

Short Answer

Expert verified
The three metal complexes were analyzed for chirality by examining their structure and checking for symmetry elements. The results are as follows: (a) square planar [Pd(en)(CN)₂] is achiral, (b) octahedral [Ni(en)(NH₃)₄]²⁺ is achiral, and (c) octahedral cis-[V(en)₂ClBr] is chiral, therefore having an optical isomer.

Step by step solution

01

Identify the metal complex geometries

Three geometries of the metal complexes are given: square planar, octahedral, and cis-octahedral. The geometry will give us insights into the spatial arrangement of the ligands which may produce chirality.
02

Analyze the geometry of [Pd(en)(CN)₂]

The square planar coordination geometry has the metal ion at the center and the four ligands are at the corners of a square on the same plane. In this case, Pd is the central metal ion, coordinated to ethylenediamine (en) and two cyanide (CN) ligands. The structure can be represented as follows: en Pd CN CN Since there is a plane of symmetry in the molecule (the plane of the paper itself), this metal complex is not chiral.
03

Analyze the geometry of [Ni(en)(NH₃)₄]²⁺

The octahedral coordination geometry consists of a central metal ion surrounded by six ligands arranged in an octahedron. In this case, Ni is the central metal ion, coordinated to one ethylenediamine (en) and four ammonia (NH₃) ligands. The structure can be represented as follows: NH₃ en NH₃ NH₃ Ni NH₃ If we consider this structure carefully, we can identify a plane of symmetry along the ligands (en) and two of the NH₃ ligands. This indicates that the metal complex is not chiral.
04

Analyze the geometry of cis-[V(en)₂ClBr]

The cis-octahedron coordination geometry also consists of a central metal ion surrounded by six ligands arranged in an octahedron, but with specific arrangements. In this case, V is the central metal ion, coordinated to two ethylenediamine (en) ligands, one chloride (Cl), and one bromide (Br) ligand, in a cis configuration. Cis configuration means that the two en ligands are adjacent to each other. The structure can be represented as follows: Cl en V en Br Since this complex does not have any plane of symmetry or inversion center, this metal complex is chiral.
05

Conclusion

On analyzing each metal complex, we can conclude that: (a) square planar [Pd(en)(CN)₂] is achiral. (b) octahedral [Ni(en)(NH₃)₄]²⁺ is achiral. (c) octahedral cis-[V(en)₂ClBr] is chiral and therefore has an optical isomer.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Optical Isomerism
Optical isomerism, a fascinating aspect of stereochemistry, is the property of certain molecules and complexes to exist in forms which are non-superimposable mirror images of one another, much like a person's left and right hands. These non-superimposable mirror images are known as 'enantiomers'. Enantiomers of a molecule or complex have identical physical and chemical properties except for the direction in which they rotate plane-polarized light. This is called optical activity, and a substance that displays this property is said to be 'optically active'.

To determine if a metal complex shows optical isomerism, we must look for elements of symmetry. If a complex lacks symmetry elements such as a plane or center of symmetry, it can be chiral and, consequently, demonstrate optical isomerism. For instance, the cis-[V(en)₂ClBr] complex has no symmetry elements and thus is chiral, capable of existing as two enantiomers. These enantiomers will rotate the plane of polarized light in opposite directions, giving them optical activity.
Coordination Compounds
Coordination compounds, also known as coordination complexes, are molecules that consist of a central metal atom or ion bonded covalently to a set of molecules or ions known as ligands. The ligands are species that can donate a pair of electrons to the metal atom, establishing the coordinate bond. The charges, if any, on the coordination complex result from the charges of the central metal ion and the total charge of the ligands attached to it.

The number of ligands attached to the metal center is termed the 'coordination number', and it plays a crucial role in determining the geometry of the complex. Coordination compounds can exhibit a variety of colors, magnetic properties, and reactivities, which makes them interesting subjects in chemistry and of immense importance in biological systems, catalysis, and materials science.
Metal Complex Geometries
The arrangement of ligands around the central metal ion in a coordination compound is described by the complex's geometry. Some typical geometries include linear, square planar, tetrahedral, and octahedral. Each geometry includes its specific spatial arrangement which influences the compound's properties and reactivity.

For example, the square planar geometry, usually observed with coordination number 4, can be found in certain metal complexes like the [Pd(en)(CN)₂] mentioned earlier. The square planar arrangement often leads to differentiated positions known as 'cis' (adjacent) and 'trans' (opposite) for the ligands. An octahedral geometry, corresponding to a coordination number of 6, has more possibilities for variation. It can lead to 'cis' and 'trans' forms, as well as 'facial' (fac) and 'meridional' (mer) isomers, depending on the relative positions of identical ligands. The specific spatial arrangements of ligands in these geometries are central to the concept of chirality in complexes, as the lack of symmetry required for optical activity depends heavily on geometry.

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Most popular questions from this chapter

Four-coordinate metals can have either a tetrahedral or a square-planar geometry; both possibilities are shown here for \(\left[\mathrm{PtCl}_{2}\left(\mathrm{NH}_{3}\right)_{2}\right] .\) (a) \(\mathrm{What}\) is the name of this molecule? (b) Would the tetrahedral molecule have a geometric isomer? (c) Would the tetrahedral molecule be diamagnetic or paramagnetic? (d) Would the square-planar molecule have a geometric isomer? (e) Would the square-planar molecule be diamagnetic or paramagnetic? (f) Would determining the number of geometric isomers help you distinguish between the tetrahedral and square-planar geometries? (g) Would measuring the molecule's response to a magnetic field help you distinguish between the two geometries? [Sections 23.4-23.6 ]

A classmate says, "A weak-field ligand usually means the complex is high spin." Is your classmate correct? Explain.

Among the period 4 transition metals \((\mathrm{Sc}-\mathrm{Zn}),\) which elements do not form ions where there are partially filled 3d orbitals?

In 2001 , chemists at SUNY-Stony Brook succeeded in synthesizing the complex trans-\(\left[\mathrm{Fe}(\mathrm{CN})_{4}(\mathrm{CO})_{2}\right]^{2-}\), which could be a model of complexes that may have played a role in the origin of life. (a) Sketch the structure of the complex. (b) The complex is isolated as a sodium salt. Write the complete name of this salt. (c) What is the oxidation state of Fein this complex? How many d electrons are associated with the Fe in this complex? (d) Would you expect this complex to be high spin or low spin? Explain.

Indicate the coordination number and the oxidation number of the metal for each of the following complexes: (a) \(\mathrm{K}_{3}\left[\mathrm{Co}(\mathrm{CN})_{6}\right]\) (b) \(\mathrm{Na}_{2}\left[\mathrm{CdBr}_{4}\right]\) (c) \(\left[\mathrm{Pt}(\mathrm{en})_{3}\right]\left(\mathrm{ClO}_{4}\right)_{4}\) (d) \(\left[\mathrm{Co}(\mathrm{en})_{2}\left(\mathrm{C}_{2} \mathrm{O}_{4}\right)\right]^{+}\) (e) \(\mathrm{NH}_{4}\left[\mathrm{Cr}\left(\mathrm{NH}_{3}\right)_{2}(\mathrm{NCS})_{4}\right]\) (f) \(\left[\mathrm{Cu}(\mathrm{bipy})_{2} \mathrm{I}\right] \mathrm{I}\)

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