Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

A certain complex of metal \(\mathrm{M}\) is formulated as \(\mathrm{MCl}_{3} \cdot 3 \mathrm{H}_{2} \mathrm{O}\). The coordination number of the complex is not known but is expected to be 4 or 6 . (a) Would conductivity measurements provide information about the coordination number? (b) In using conductivity measurements to test which ligands are bound to the metal ion, what assumption is made about the rate at which ligands enter or leave the coordination sphere of the metal?

Short Answer

Expert verified
Conductivity measurements can provide information about the coordination number of the metal complex MCl3·3H2O since the number of charged species in solution and their respective charges depend on the coordination number. In this case, coordination numbers 4 and 6 would produce different charges upon dissolution. When using conductivity measurements to study ligands bound to the metal ion, the main assumption made is that the rate of ligand exchange is either slow enough or fast enough so as not to interfere with the measurements. This allows us to interpret the conductivity data without considering possible changes in concentration due to ligand exchange during the measurement.

Step by step solution

01

(a) Information on coordination number from conductivity measurements

Conductivity measurements determine the ability of a solution to conduct electric current. In the context of a metal complex, the conductivity depends on the concentration of charged species, including the metal ion and its counterion(s), and the mobility of these species within the solution. For the metal complex MCl3·3H2O, the observed conductivity would depend on the number of ions formed upon dissolving in water and their respective charges. If the coordination number affects the number of charged species in solution, then the conductivity measurements could potentially provide information about the coordination number. Let's consider the two given possibilities for coordination numbers: 1. Coordination number = 4: In this case, the complex could be [MCl2(H2O)2]Cl·H2O, which dissolves to produce three charged species: [MCl2(H2O)2]^+, Cl^-, and H2O molecules. The total charge produced is +1. 2. Coordination number = 6: In this case, the complex could be [MCl3(H2O)3], which does not dissolve into separate ions as all the ligands are bound to the metal ion. So, the total charge produced is 0. From the above possibilities, we can see that the coordination number affects the charged species upon dissolution and their respective charges. Therefore, conductivity measurements can provide information about the coordination number.
02

(b) Assumptions regarding ligand exchange

When using conductivity measurements to study ligands bound to the metal ion, the main assumption made is that the rate of ligand exchange, or the rate at which ligands enter or leave the coordination sphere of the metal, is either slow enough or fast enough so as not to interfere with the measurements. This means that the metal complex should either reach equilibrium (complete ligand exchange) quickly, or the rate of ligand exchange should be slow enough that it doesn't affect the measured conductivity values. This assumption allows us to interpret the conductivity data without considering any possible changes in the concentration of the complex and its charged species due to ligand exchange during the measurement. In summary, conductivity measurements can be used to gather information about the coordination number and ligands bound to the metal ion, provided certain assumptions, mainly about the ligand exchange rate, are fulfilled.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

Key Concepts

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

Conductivity Measurements
Conductivity measurements are a fascinating tool used to study metal complexes. These measurements involve assessing a solution's ability to conduct an electric current. When a metal complex dissolves in water, it breaks down into ions. The concentration and mobility of these ions in the solution will affect how well it conducts electricity.

In coordination chemistry, the composition of these ions can hint at the inner workings of the metal complex. Specifically, it can provide clues about the coordination number, which is the number of ligand atoms that are attached directly to the central metal atom. By analyzing the charged particles resulting from the dissolution of the complex and their movement, we can gain insights into the configuration and behavior of the complex.
  • More ions in a solution often lead to higher conductivity.
  • Various dissolution patterns connect to different potential structures of the complex.
Understanding the basics of conductivity measurements helps in making educated assumptions about a complex's structure and its stoichiometry in different environments.
Coordination Number
The coordination number in a coordination complex is an essential concept that defines the number of ligand atoms bonded directly to the central metal ion. It significantly influences the geometry and reactivity of metal complexes.

Usually, common coordination numbers are 4 and 6. A coordination number of 4 could lead to structures such as square planar or tetrahedral. In contrast, a coordination number of 6 typically forms octahedral complexes. These configurations deeply affect the properties and stability of the metal complexes.
  • A higher coordination number can sometimes lead to closer-packed structures.
  • The geometry influences the electronic properties of the metal ion.
Knowing the coordination number helps predict how a metal complex will behave in reactions and how it might interact with other compounds.
Ligand Exchange
Ligand exchange is an intriguing phenomenon in coordination chemistry, where ligands bonded to a metal complex are replaced by other ligands. This process can vary in speed, greatly affecting how metal complexes are studied through techniques like conductivity measurements.

The assumption behind measuring conductivity in ligand exchange studies is that the exchange process is either very fast or very slow. This ensures that modifications to the complex do not significantly alter the conductivity during the measurement. There are a few factors to bear in mind:
  • Fast exchanges might reach equilibrium rapidly, stabilizing the observation phase.
  • Slow exchanges guarantee that the dissolution forms a consistent pattern.
Interpretations based on ligand exchange assume that these rates will not distort the concentration of ions and distort the results, allowing clearer insights into the workings of the complex.
Metal Complexes
Metal complexes are fascinating assemblies formed when metal ions bind with ligands, which are molecules or ions that donate electron pairs to the metal. These complexes are crucial in many chemical reactions and scenarios, such as catalysis, biological systems, and materials science.

Key components of metal complexes include:
  • Central Metal Ion: Often a transition metal, serving as the focal bonding point.
  • Ligands: Molecules or ions that coordinate to the metal through a Lewis acid-base interaction.
  • Coordination Sphere: Outlines the spatial arrangement and the types of ligand bonds surrounding the metal.
The behavior and properties of metal complexes, such as color, magnetism, and reactivity, are influenced by the structure and type of ligands attached to them. Understanding their form elucidates many reactions pivotal to both synthetic and natural processes.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Explain why the \(d_{x y}, d_{x z}\), and \(d_{y z}\) orbitals lie lower in energy than the \(d_{z^{2}}\) and \(d_{x^{2}-y^{2}}\) orbitals in the presence of an octahedral arrangement of ligands about the central metalion.

Sketch all the possible stereoisomers of (a) tetrahedral \(\left[\mathrm{Cd}\left(\mathrm{H}_{2} \mathrm{O}\right)_{2} \mathrm{Cl}_{2}\right]\), (b) square-planar \(\left[\mathrm{IrCl}_{2}\left(\mathrm{PH}_{3}\right)_{2}\right]^{-}\), (c) octa- hedral \(\left[\mathrm{Fe}(0 \text { -phen })_{2} \mathrm{Cl}_{2}\right]^{+}\)

Consider an octahedral complex \(\mathrm{MA}_{3} \mathrm{~B}_{3}\). How many geometric isomers are expected for this compound? Will any of the isomers be optically active? If so, which ones?

Sketch the structure of the complex in each of the following compounds: (a) \(c i s-\left[\mathrm{Co}\left(\mathrm{NH}_{3}\right)_{4}\left(\mathrm{H}_{2} \mathrm{O}\right)_{2}\right]\left(\mathrm{NO}_{3}\right)_{2}\) (b) \(\mathrm{Na}_{2}\left[\mathrm{Ru}\left(\mathrm{H}_{2} \mathrm{O}\right) \mathrm{Cl}_{5}\right]\) (c) \(\operatorname{trans}-\mathrm{NH}_{4}\left[\mathrm{Co}\left(\mathrm{C}_{2} \mathrm{O}_{4}\right)_{2}\left(\mathrm{H}_{2} \mathrm{O}\right)_{2}\right]\) (d) \(c i s-\left[\operatorname{Ru}(e n)_{2} C l_{2}\right]\)

The complexes \(\left[\mathrm{V}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{3+}\) and \(\left[\mathrm{VF}_{6}\right]^{3-}\) are both known. (a) Draw the \(d\) -orbital energy-level diagram for \(\mathrm{V}(\mathrm{III})\) octahedral complexes. (b) What gives rise to the colors of these complexes? (c) Which of the two complexes would you expect to absorb light of higher energy? Explain.

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free