explain the locking of conformation
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Conformations that correspond to local maxima on the energy surface are the transition states between the local-minimum conformational isomers. Rotations about single bonds involve overcoming a rotational energy barrier to interconvert one conformer to another.
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For locking of conformation, we have to consider the following points.
- Confirmation means an infinite number of possible spatial arrangements of the atoms in a molecule.
- The isomers can be interconverted by the rotation of their constituent group about a single bond.
- Locking of conformation observed in Cyclohexane.
- Cyclohexane may acquire either axial or equatorial positions.
- In 1,3-diaxial, interaction becomes intense due to the presence of internal butane gauche interaction. So stability decreased.
- Therefore large substituents like t-butyl prefer equatorial positions to avoid di-axial interactions.
- And existence in only one conformation is termed as locking of conformation.
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