A classmate says, "A strong-field ligand means that the ligand binds strongly to the metal ion." Is your classmate correct? Explain.

Short Answer

Expert verified
While a strong-field ligand does cause larger d-orbital splitting in the metal ion, it does not necessarily mean that the ligand binds more strongly to the metal ion. The classmate's statement confuses these two concepts and is not entirely correct.

Step by step solution

01

Understanding Strong-Field Ligands

Strong-field ligands are ligands that lead to a large energy gap between the metal ion d-orbital levels in coordination compounds. This means that these ligands lead to higher splitting in the d-orbitals compared to weak-field ligands.
02

Crystal Field Theory

Crystal field theory is a model used to explain the electronic structure of coordination compounds formed between metal ions and ligands. According to this theory, when the ligand donor atoms approach the central metal ion, the d-orbitals of the metal ion split into different energy levels depending on their spatial orientation. This splitting can be small (with weak-field ligands) or large (with strong-field ligands).
03

Spectrochemical Series

The Spectrochemical series is a list of ligands arranged in the order of increasing field strength. Ligands on the left side of the series (such as I-, Br-, and Cl-) are considered weak-field ligands, while those on the right side (such as CN-, CO, and NO+) are considered strong-field ligands. The field strength of a ligand determines the extent of d-orbital splitting in a coordination compound.
04

Analyzing the Statement

Now, let us analyze the given statement: "A strong-field ligand means that the ligand binds strongly to the metal ion." The statement seems to confuse the concept of strong-field ligands (which lead to larger d-orbital splitting) with the strength of bonding between the ligand and the metal ion. The strong-field ligands indeed lead to higher d-orbital energy gaps in metal ions, but this is not a direct indication of the bond strength between the ligand and the metal ion. A ligand that causes large splitting in d-orbitals might have a stronger effect on the electronic structure of the metal ion, but it does not translate to stronger binding. Thus, the classmate's statement is not fully correct, as there might not be a direct correlation between these two characteristics. In conclusion:
05

Final Answer

While a strong-field ligand does cause larger d-orbital splitting in the metal ion, it does not necessarily mean that the ligand binds more strongly to the metal ion. The classmate's statement confuses these two concepts, and thus is not entirely correct.

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Most popular questions from this chapter

Write balanced chemical equations to represent the following observations. (In some instances the complex involved has been discussed previously in the text.) (a) Solid silver chloride dissolves in an excess of aqueous ammonia. (b) The green complex \(\left[\mathrm{Cr}(\mathrm{en})_{2} \mathrm{Cl}_{2}\right] \mathrm{Cl},\) on treatment with water over a long time, converts to a brown-orange complex. Reaction of \(\mathrm{AgNO}_{3}\) with a solution of the product precipitates \(3 \mathrm{~mol}\) of AgCl per mole of Cr present. (Write two chemical equations.) (c) When an NaOH solution is added to a solution of \(\mathrm{Zn}\left(\mathrm{NO}_{3}\right)_{2},\) a precipitate forms. Addition of excess \(\mathrm{NaOH}\) solution causes the precipitate to dissolve. (Write two chemical equations.) (d) A pink solution of \(\mathrm{Co}\left(\mathrm{NO}_{3}\right)_{2}\) turns deep blue on addition of concentrated hydrochloric acid.

In crystal-field theory, ligands are modeled as if they are point negative charges. What is the basis of this assumption, and how does it relate to the nature of metal-ligand bonds?

(a) What is the difference between Werner's concepts of primary valence and secondary valence? What terms do we now use for these concepts? (b) Why can the \(\mathrm{NH}_{3}\) molecule serve as a ligand but the \(\mathrm{BH}_{3}\) molecule cannot?

(a) What is meant by the term chelate effect? (b) What thermodynamic factor is generally responsible for the chelate effect? (c) Why are polydentate ligands often called sequestering agents?

(a) Sketch a diagram that shows the definition of the crystal-field splitting energy \((\Delta)\) for an octahedral crystal field. (b) What is the relationship between the magnitude of \(\Delta\) and the energy of the d- \(d\) transition for a \(d^{1}\) complex? (c) Calculate \(\Delta\) in \(\mathrm{kJ} / \mathrm{mol}\) if a \(d^{1}\) complex has an absorption maximum at \(545 \mathrm{nm}\).

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