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The d-orbitals involved in \[s{{p}^{3}}{{d}^{2}}\] or \[{{d}^{2}}s{{p}^{3}}\] hybridization of the central metal ion are:
(this question has multiple correct options)
a.) \[{{d}_{{{x}^{2}}-{{y}^{2}}}}\]
b.) \[{{d}_{xy}}\]
c.) \[{{d}_{yz}}\]
d.) \[{{d}_{{{z}^{2}}}}\]

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Answer
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Hint: From the given hybridization we can say that the geometry of the compound has octahedral. So, to solve this question, consider the splitting of d-orbitals in an octahedral complex, when approached by a ligand.


Complete step by step solution:
When any negatively charged species or ligand approaches a metal, the energy of the orbitals increases. This leads to the splitting of orbitals as –
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In octahedral complexes, the splitting of orbitals always takes place in this manner.
The electron first goes to the lower energy orbital, i.e. \[{{d}_{xy}}\].\[{{d}_{yz}}\],\[{{d}_{{{z}^{2}}}}\]and then to the higher energy orbital, i.e., \[{{d}_{{{x}^{2}}-{{y}^{2}}}}\]and \[{{d}_{{{z}^{2}}}}\]. Therefore, bonding electrons go to the high energy orbitals which decide the hybridization of the compound.
In case of \[s{{p}^{3}}{{d}^{2}}\] hybridization, nd (outermost) orbitals are involved. The compound is therefore also known as outer-orbital complex.
In case of \[{{d}^{2}}s{{p}^{3}}\] hybridization, (n-1)d (next to outermost) orbitals are involved. The compound is therefore also known as inner-orbital complex.
Therefore, the answer is – option (a) and option (d).

Additional information: In short, if inner d-orbital is used for bonding, the hybridization will be \[{{d}^{2}}s{{p}^{3}}\]. Similarly, if outer d-orbital is used, the hybridization will be \[s{{p}^{3}}{{d}^{2}}\].

Note: Irrespective of the differences between \[s{{p}^{3}}{{d}^{2}}\] and \[{{d}^{2}}s{{p}^{3}}\], there are certain similarities, such as –
Both hybridization results in octahedral geometry.
Both have six hybrid orbitals.
There is an angle of 90 degrees between hybrid orbitals.