[Western Oregon University]

Lecture Notes on Conformations of Cycloalkanes

SHAPES OF CYCLOALKANES

Are the rings planar or nonplanar?

 


Cyclohexane has a heat of combustion that is about the same as for an unbranched alkane

CONFORMATIONS OF CYCLOHEXANE


Heat of Combustion Data suggests that cyclohexane is free of angle strain.

To get tetrahedral geometries for the carbons, the ring must be nonplanar.
 
 
 

 

AXIAL & EQUITORIAL BONDS IN CYCLOHEXANE

 

 
 
 
 
 
 
 
 

CONFORMATIONAL INVERSION OR "RING-FLIPPING" IN CYCLOHEXANE

 
 
In the ring-flipping process, the chair goes through the following conformations:
  • half-chair
  • boat
  • half-chair
to get to the other chair conformation

CONFORMATIONAL ANALYSIS OF MONOSUBSTITUTED CYCLOHEXANES


The most stable conformation is a chair with the substituent occupying an equitorial position
 
 
 
Constitutional isomers differ in the order of their atomic connections.

Stereoisomers have their atoms bonded in the same order, but they differ in the arrangement of atoms in space.
The compound in the box exists as a pair of stereoisomers.
 
The cis isomer is less stable due to steric crowding.

DISUBSTITUTED CYCLOHEXANES

 
 
 
 
 
 
 
 
 
 
 
 





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