EXPLAIN SP 3 D HYBRIDITION WITH AN EXAMPLE .

Sp3d hybridization: In sp3d hybridization, one 's', three 'p' and one 'd' orbitals of almost equal energy intermix to give five identical and degenerate hybrid orbitals, which are arranged in trigonal bipyramidal symmetry. Among them, three are arranged in trigonal plane and the remaining two orbitals are present above and below the trigonal plane at right angles. The sp3d hybrid orbitals have 20% 's', 60% 'p' and 20% 'd' characters.

Example: PCl5

  • The ground state electronic configuration of phosphorus atom is: 1s2 2s22p6 3s23px13py13pz1

  • The formation of PCl5 molecule requires 5 unpaired electrons. Hence the phosphorus atom undergoes excitation to promote one electron from 3s orbital to one of empty 3d orbital.

  • Thus the electronic configuration of 'P' in the excited state is 1s2 2s22p6 3s23px13py13pz1 3d1.

  • In the excited state, intermixing of a 3s, three 3p and one 3d orbitals to give five half filled sp3d hybrid orbitals, which are arranged in trigonal bipyramidal symmetry.

  • i.e., Three orbitals are arranged in trigonal planar symmetry, whereas the remaining two are arranged perpendicularly above and below this plane. 

  • By using these half filled sp3d orbitals, phosphorous forms five σsp3d-p bonds with chlorine atoms. Each chlorine atom makes use of half filled 3pz orbital for the bond formation. 

  • The shape of PCl5 molecule is trigonal bipyramidal with 120o and 90o of ∠Cl - P - Cl bond angles.

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The term “sp3 hybridization” refers to the mixing character of one 2s-orbital and three 2p-orbitals to create four hybrid orbitals with similar characteristics. In order for an atom to be sp3 sp3 hybridization

Now let's see how hydridisation can account for each of these features, working towards methane then other alkanes: 
 

the concept of hybridization
  • Promote an electron from 2s to 2p to create an excited state...
    • with 4 unpaired electrons we can form 4 bonds
    • these bonds would be from 1 x C2s-H1s interaction and 3 x C2p-H1s interactions
    • but these bonds will have different lengths and strengths
    • the 3 C-H bonds from the p orbitals maybe expected to have H-C-H bond angles of 90 degrees
  • "Blend" (i.e. hybridise) the s and the three p orbitals...
    • since we "mixed" 4 orbitals, we get a set of 4 sporbitals
    • each sp3 hybrid contains a single unpaired electron
a sp3 hydrid orbital
creating the hybrids from an s and 3 p orbitals
The sphybrid orbital looks like a "distorted" p orbital with unequal lobes.

The 4 sp3 hybrids point towards the corners of a tetrahedron. 
 


 
 


  • For methane:
    • 4 equivalent C-H s bonds can be made by the interactions of Cspwith a H1s
orbitals to bonds for methane
  
  • Now ethane, H3C-CH3 as a model for alkanes in general:
    • Both C are sp hybridised.
    • C-H s bonds are made by the interaction of C spwith H1s orbitals (see the red arrows)
    • C-C s bond is made by the interaction of C spwith another C sporbital (see the green arrow)
orbitals to bonds for ethane

hybridized, it must have an s orbital and three p orbitals.

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