Stability ā Chelate effect, stability constants
Coordination Compounds
15
JEE Qs
8%
Hard
60
min
Focus on understanding the thermodynamic basis (entropy) of the chelate effect and how to compare stability using given stability constant values and ligand properties.
š§® Key Formulas
ā Key Points for JEE
- 1The Chelate Effect is the enhanced stability of a coordination complex containing a chelate ligand (polydentate ligand) compared to an analogous complex with only monodentate ligands.
- 2The primary thermodynamic reason for the chelate effect is a favorable entropy change (ĪS > 0), as one polydentate ligand replaces multiple solvent molecules, leading to an increase in the number of particles in solution.
- 3Stability constants (stepwise K_n and overall β_n) are equilibrium constants for the formation of a complex; a higher value indicates greater thermodynamic stability.
- 4Chelate rings of 5 or 6 members are generally the most stable due to minimal ring strain, while 4-membered rings are highly strained and larger rings offer less entropic advantage.
- 5Factors increasing complex stability include: higher charge on the central metal ion, smaller size of the metal ion (higher charge density), stronger basicity/donor strength of the ligand, and the presence of chelate rings.
ā ļø Common Mistakes
- āConfusing thermodynamic stability (equilibrium constants) with kinetic stability (lability/inertness) of coordination complexes.
- āIncorrectly assuming all chelate complexes are equally stable; the number and size of chelate rings significantly impact stability.
- āOverlooking the entropic contribution to the chelate effect, often focusing solely on the enthalpy of bond formation.
- āMistaking stepwise stability constants (K_n) for overall stability constants (β_n) or miscalculating β_n from K_n values.
š Practice Questions
See allQ74.In the Claisen-Schmidt reaction to prepare, dibenzalacetone from 5.3 g of benzaldehyde, a total of 3.51 g of product was obtained. The percentage yield in this reaction was ______ %.
Q61.The calculated spin-only magnetic moments of K3 [Fe(OH)6] and K4 [Fe(OH)6] respectively are : (1) 3.87 and 4.90 B.M. (2) 4.90 and 5.92 B.M. (3) 4.90 and 4.90 B.M. (4) 5.92 and 4.90 B.M.
Q54.Identify the homoleptic complexes with odd number of d electrons in the central metal : (A) [FeO4]2ā (B) [Fe(CN)6]3ā (C) [Fe(CN)5NO]2ā (D) [CoCl4]2ā (E) [Co(H2O)3 F3] Choose the correct answer from the options given below : (1) (A), (B) and (D) only (2) (C) and (E) only (3) (B) and (D) only (4) (A), (C) and (E) only
Q68.In which of the following complexes the CFSE, Īo will be equal to zero? (1) [Fe(en)3]Cl3 (2) K4 [Fe(CN)6] (3) [Fe(NH3)6]Br2 (4) K3 [Fe(SCN)6]
Q70.From the magnetic behaviour of [NiCl4]2ā (paramagnetic) and [Ni(CO)4] (diamagnetic), choose the correct geometry and oxidation state. (1) [NiCl4]2ā: NiII , tetrahedral [Ni(CO)4] : NiII , (2) [NiCl4]2ā : NiII , square planar [Ni(CO)4] : Ni(0) square planar , square planar (3) [NiCl4]2ā: NiII , tetrahedral [Ni(CO)4] : Ni(0), (4) [NiCl4]2ā: Ni(0), tetrahedral [Ni(CO)4] : Ni(0), tetrahedral square planar
Q53.The correct order of the following complexes in terms of their crystal field stabilization energies is : (1) [Co(NH3)4]2+ < [Co(NH3)6]2+ < [Co(en)3]3+ < [Co(NH3)6]3+ (2) [Co(NH3)6]2+ < [Co(NH3)6]3+ < [Co(NH3)4]2+ < [Co(en)3]3+ (3) [Co(en)3]3+ < [Co(NH3)6]3+ < [Co(NH3)6]2+ < [Co(NH3)4]2+ (4) [Co(NH3)4]2+ < [Co(NH3)6]2+ < [Co(NH3)6]3+ < [Co(en)3]3+
NCERT Chapters
- Class 12 Chemistry Ch 9: Coordination Compounds