In the chair form of cyclohexane ring bonds to ring atoms (and molecular entities
attached to such bonds) are termed axial or
equatorial according to whether the bonds make a relatively large or small
angle, respectively, with the plane containing or passing closest to a majority of the
ring atoms. Thus the axial bonds are approximately parallel to the
C3 axis and the
equatorial bonds approximately parallel to two of the ring bonds. These terms are also used
for the chair form of other saturated six-membered rings. The corresponding bonds
occurring at the allylic positions in mono-unsaturated six-membered rings are termed
pseudo-axial (or quasi-axial) and pseudo-equatorial (or quasi-equatorial). The terms
axial and
equatorial have similarly been used in relation to the puckered
conformation of cyclobutane,
crownconformer of cyclooctane, etc. and the terms pseudo-axial and pseudo-equatorial in the context
of the non-planar structures of cyclopentane and cycloheptane.
See
apical (basal, equatorial) for an alternative use of axial and
equatorial with bipyramidal structures.
Source:
PAC, 1996, 68, 2193
(Basic terminology of stereochemistry (IUPAC Recommendations 1996))
on page 2200