CUET · CHEMISTRY · PYQ PAPER 2025
Colligative properties are applicable to:
- A dilute solution
- B solid solutions
- C concentrated solutions
- D only aqueous solution
Answer & Solution
Correct Answer
(A) dilute solution
Step-by-step Solution
Detailed explanation
dilute solution
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More questions from CHEMISTRY
- Werner was the first to describe the bonding features in coordination compounds. But his theory could not answer basic questions like :
(i) Why only certain elements possess the remarkable property of forming coordination compounds ?
(ii) Why the bonds in coordination compounds have directional properties ?
(iii) Why coordination compounds have characteristics magnetic and optical properties ?
Many approaches have been put forth to explain the nature of bonding in coordination compounds viz. Valence Bond Theory (VBT), Crystal Field Theory (CFT), Ligand Field Theory (LFT) and Molecular Orbital Theory (MOT).
We shall focus our attention on elementary treatment of the application of VBT and CFT to coordination compounds.
According to this theory, the metal atom or ion under the influence of ligands can use its ( \(n -1\) )d, ns np or ns, np, nd orbitals for hybridisation to yield a set of equivalent orbitals of definite geometry such as octahedral, tetrahedral, square planar and so on.
These hybridised orbitals are allowed to overlap with ligand orbitals that can donate electron pairs for bonding.
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According to Valence Bond theory, the metal atom or ion under the influence of ligands can use its ( \(n-1\) )d, ns, np or \(n s, n p, n d\) orbitals for hybridisation to yield a set of equivalent orbitals of definite geometry such as octahedral, tetrahedral, square planar and so on. These hybridised orbitals are allowed to overlap with ligand orbitals that can donate electron pairs for bonding. While the VB theory, to a larger extent, explains the formation, structures and magnetic behaviour of coordination compounds, it suffers from the many shortcomings. The Crystal field theory (CFT) is an electrostatic model which considers the metal-ligand bond to be ionic arising purely from electrostatic interactions between the metal ion and the ligand. The five \(d\) orbitals in an isolated gaseous metal atom/ion have same energy, i.e., they are degenerate. This degeneracy is maintained if a spherically symmetrical field of negative charges surrounds the metal atom/ion. However, when this negative field is due to ligands in a complex, it becomes asymmetrical and the degeneracy of the \(d\) orbitals is lifted. It results in splitting of the \(d\) orbitals. The pattern of splitting depends upon the nature of the crystal field.
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