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(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?

Short Answer

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(a) The chelate effect is the increased stability of a complex formed by a polydentate ligand when compared to a complex formed by monodentate ligands, due to the formation of a ring structure. (b) The thermodynamic factor responsible for the chelate effect is entropy, as the reaction with polydentate ligands produces fewer particles, leading to an increase in entropy. (c) Polydentate ligands are called sequestering agents because they form stable ring structures with metal ions, effectively trapping and controlling their availability in various systems.

Step by step solution

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(a) Defining the Chelate Effect

The chelate effect refers to the increased stability of a complex formed by a polydentate (multi-dentate) ligand when compared to the stability of a complex formed by an equivalent combination of monodentate (single-dentate) ligands. A chelate complex is formed when a polydentate ligand coordinates with a central metal ion and forms a ring structure.
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(b) Thermodynamic Factor Responsible for the Chelate Effect

The chelate effect is generally attributed to entropy. When a polydentate ligand forms a complex with a metal ion, fewer particles are produced compared to the reaction with monodentate ligands. The increase in entropy due to the release of a larger number of displaced monodentate ions or molecules is mainly responsible for the higher stability of the chelate complexes.
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(c) Polydentate Ligands as Sequestering Agents

Polydentate ligands are often called sequestering agents because they can form stable ring structures with a central metal ion, effectively "sequestering" or trapping the metal ion in a chelate complex. This strong binding makes it difficult for the metal ion to participate in any undesired reactions, hence controlling its availability in systems such as industrial processes, biochemistry, and environmental chemistry.

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Most popular questions from this chapter

When Alfred Werner was developing the field of coordination chemistry, it was argued by some that the optical activity he observed in the chiral complexes he had prepared was because of the presence of carbon atoms in the molecule. To disprove this argument, Werner synthesized a chiral complex of cobalt that had no carbon atoms in it, and he was able to resolve it into its enantiomers. Design a cobalt(III) complex that would be chiral if it could be synthesized and that contains no carbon atoms. (It may not be possible to synthesize the complex you design, but we won't worry about that for now.)

Which of the following objects is chiral? (a) a left shoe, (b) a slice of bread, (c) a wood screw, (d) a molecular model of Zn(en)Cl2, (e) a typical golf club.

Polydentate ligands can vary in the number of coordination positions they occupy. In each of the following, identify the polydentate ligand present and indicate the probable number of coordination positions it occupies: (a) [Co(NH3)4(0phen)]Cl3 (b) [Cr(C2O4)(H2O)4]Br (c) [Cr(EDTA)(H2O)] (d) [Zn(en)2](ClO4)2

(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 NH3 molecule serve as a ligand but the BH3 molecule cannot?

A four-coordinate complex MA2 B2 is prepared and found to have two different isomers. Is it possible to determine from this information whether the complex is square planar or tetrahedral? If so, which is it?

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