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Spin pairing and overlapping theory cann...

Spin pairing and overlapping theory cannot explain the equal bond length as well as equal bond angles in `CH_(4)` molecule. To explain the above facts we are in need of hybridization theory. Hybridization is the mixing of atomic orbitals of comparable energy and the numbe of atomic orbitals involved is equal to the number of hybrid orbitals formed of equal energy.
Increasing order of the energy of hybrid orbitals is :

A

`sp^(3)ltsp^(2)ltsp`

B

`sp^(2)ltsp^(3)ltsp`

C

`spltsp^(3)ltsp^(2)`

D

`spltsp^(2)ltsp^(3)`

Text Solution

Verified by Experts

The correct Answer is:
D

sp orbital is closer to nucleus, so has lower energy.
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Spin pairing and overlapping theory cannot explain the equal bond length as well as equal bond angles in CH_(4) molecule. To explain the above facts we are in need of hybridization theory. Hybridization is the mixing of atomic orbitals of comparable energy and the numbe of atomic orbitals involved is equal to the number of hybrid orbitals formed of equal energy. According to hybridization theory, the %s character in sp^(3) hybrid orbitals is :

Spin pairing and overlapping theory cannot explain the equal bond length as well as equal bond angles in CH_(4) molecule. To explain the above facts we are in need of hybridization theory. Hybridization is the mixing of atomic orbitals of comparable energy and the numbe of atomic orbitals involved is equal to the number of hybrid orbitals formed of equal energy. The number of axial and equatorial positions in trigonal bipyramidal geometry having sp^(3)d hybridizaton are respectively :

The decreasing order of electronegativity of the hybrid orbitals is :

The number of hybrid orbitals in a molecule of decane are

The number of sp^(2) hybrid orbitals in a molecule of benzene is :

Number of hybrid orbitals present in a molecule of propene are

Number of hybrid orbitals formed in 'sp' hybridisation of carbon are

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