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What is Hybridization?

Hybridization is a concept in valence bond theory that involves mixing atomic orbitals (with varied energies or shapes) to produce new hybrid orbitals suitable for electron pairing to create chemical bonds.

The act of courtship is comparable to the establishment of bonds. Atoms move closer together, attract each other, and progressively lose a small portion of their mass to the other atoms. Hybridisation, or the study of bonding, is significant in chemistry. During bonding, what happens to the atoms? The concept of hybridisation holds the key to the solution. Let’s discuss hybridisation in detail.

What is Hybridisation?

All of the elements in our environment behave in unusual and unexpected ways. The electrical configuration of these elements and their properties is a fascinating subject to investigate. We can draw various practical applications of such elements because of the distinctiveness of their features and usage. When it comes to the details in our environment, we can see a wide range of physical qualities. The study of hybridisation and how it allows for the fascinating mixture of multiple molecules is crucial in science.

Understanding the properties of hybridisation allows us to go into the realms of science in a way that is difficult to grasp at first but rewarding to study as we learn more. 

In 1931, Scientist Pauling proposed the evolutionary notion of hybridisation. He used the term “hybridisation” to describe the process of altering the energy of specific atoms’ orbitals to create new orbitals of equivalent energy. As a result of this technique, new orbitals known as hybrid orbitals emerge.

Uses

Hybridisation aids in the prediction of molecular form, especially in organic chemistry. Although the electrons originated from both 2s and 2p orbitals, Linus Pauling noticed that all bond angles in a molecule, such as carbon tetrachloride (CCl4), are the same.

“The tetrahedral orbitals of s and p are just the best adapted for creating strong bonds of all the potential hybrid orbitals,” Pauling adds. The bond angles around a tetrahedral carbon are commonly between 106º and 113º, even in asymmetrical compounds. Pauling continues to examine bond angles that seem significantly different from tetrahedral values, such as cyclopropane, and how the strain in these bonds makes them less stable and hence more easily broken.

Five Basic Shapes of Hybridisation

Linear, trigonal planar, tetrahedral, trigonal bipyramidal, and octahedral seem to be the five basic shapes of hybridisation.

  • Linear: Two electron groups are involved for sp hybridisation, and also, the angle here between orbitals is 180°.
  • Trigonal planar: Three electron groups generate sp² hybridisation, with just a 120° angle among orbitals here.
  • Tetrahedral: In sp³ hybridisation, four-electron groups are involved, with a 109.5° angle across orbitals.
  • Trigonal bipyramidal: Five electron groups are involved in sp³d hybridisation, which results in a 90° to 120° angle between orbitals.
  • Octahedral: Six electron groups are involved in the sp³d² hybridisation, with a 90° angle between orbitals.

Bent’s Rule

This dynamic relationship among hybridisation and other characteristics characterising the atom or molecule, including shape, energy, and spectroscopic properties, is affected by external or internal perturbations. A “small” shift in hybridisation may cause considerable variations in chemical characteristics that can be measured directly using secondary kinetic isotope effects in the lab.

The well-established relationship between hybridisation and electronegativity, known as Bent’s rule, considerably increases the effectiveness of hybridisation-based structural research in organic chemistry.

This rule indicates that atoms drive hybrid orbitals with more p character towards a more electronegative, or that s character accumulates in orbitals oriented towards electropositive substituents. An earlier computational study discovered a strong link between carbon hybridisation and the electronegativity of Y in monosubstituted alkanes, alkenes, and alkynes’ C–Y bonds.

Even though Bent’s rule describes a wide range of hybridisation effects utilised in organic compound reactivity management, the link between hybridisation with electronegativity has not been generally applied to non-carbon systems (except for a few notable exceptions, especially the recent extension to transition metal compounds).

A large study that uses modern computational techniques to verify the general applicability of Bent’s rule to main group elements other than carbon and correspond trends in orbital hybridisation to observable electronic and structural parameters could be advantageous in advancing a much more unified structural chemistry foundation. The closure of this gap will provide a framework for the structural investigation of a wide range of molecular systems across the periodic system.

Conclusion

Hybridisation is joining two atomic orbitals to form a new type of hybridised orbitals in chemistry. This combining frequently results in the formation of hybrid orbitals with radically different energies, geometries, etc. The majority of hybridisation occurs between atomic orbitals of the same energy level. As a result, if the energies of filled and half-filled orbitals are equal, they can initiate the process. I hope now you have got all the necessary information regarding hybridisation. For better understanding, you must read the topic thoroughly.