180° angle between the two chlorine atoms in the diequatorial conformation of trans-1,2-dichlorocyclohexane.
- conformatio Results from bond rotation, they may be interconverted by bond rotation but interconversion does NOT require the breaking of bonds, Virtually every molecule, except the simplest and most rigid, has many possible conformations
- In it the bond rotates and interactions between atoms and their electron clouds create torsional strain and steric strain in the molecule and the preferred conformations are those of lower energy where strain is minimized.
- the less stearic hindrance the most stable configuration, the big molecules create the most stearic hindrance
- dipole moment also defines the stability of conformational structure.
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