Stereoisomers are isomeric molecules that have the same molecular formula and sequence
of bonded atoms, but that differ only in the three-dimensional orientations of their atoms
in space.
This contrasts with structural isomers, which share the same molecular formula, but the
bond connections or their order differs.
By definition, molecules that are stereoisomers of each other represent the same structural
isomer.
Enantiomers
Enantiomers are two stereoisomers that are related to each other by a reflection: They
are mirror images of each other, which are non-superimposable.
Human hands are a macroscopic analog of stereoisomerism.
Every stereogenic center in one has the opposite configuration in the other.
Two compounds that are enantiomers of each other have the same physical properties, except
for the direction in which they rotate polarized light and how they interact with different
optical isomers of other compounds.
As a result, different enantiomers of a compound may have substantially different biological
effects.
Pure enantiomers also exhibit the phenomenon of optical activity and can be separated only
with the use of a chiral agent.
In nature, only one enantiomer of most chiral biological compounds, such as amino acids,
is present.
Diastereomers
Diastereomers are stereoisomers not related through a reflection operation.
They are not mirror images of each other.
These include meso compounds, cis–trans isomers, and non-enantiomeric optical isomers.
Diastereomers seldom have the same physical properties.
In the example shown below, the meso form of tartaric acid forms a diastereomeric pair
with both levo and dextro tartaric acids, which form an enantiomeric pair.
It should be carefully noted here that the D- and L- labeling of the isomers above is
not the same as the d- and l- labeling more commonly seen, explaining why these may appear
reversed to those familiar with only the latter naming convention.
Please refer to Chirality for more information regarding the D- and L- labels.
Cis–trans and E-Z isomerism
Stereoisomerism about double bonds arises because rotation about the double bond is
restricted, keeping the substituents fixed relative to each other.
If the two substituents on at least one end of a double bond are the same, then there
is no stereoisomer and the double bond is not a stereocenter, e.g. propene, CH3CH=CH2
where the two substituents at one end are both H.
Traditionally, double bond stereochemistry was described as either cis or trans, in reference
to the relative position of substituents on either side of a double bond.
The simplest examples of cis-trans isomerism are the 1,2-disubstituted ethenes, like the
dichloroethene isomers shown below.
Molecule I is cis-1,2-dichloroethene and molecule II is trans-1,2-dichloroethene.
Due to occasional ambiguity, IUPAC adopted a more rigorous system wherein the substituents
at each end of the double bond are assigned priority based on their atomic number.
If the high-priority substituents are on the same side of the bond, it is assigned Z.
If they are on opposite sides, it is E. Since chlorine has a larger atomic number than hydrogen,
it is the highest-priority group.
Using this notation to name the above pictured molecules, molecule I is-1,2-dichloroethene
and molecule II is-1,2-dichloroethene.
It is not the case that Z and cis or E and trans are always interchangeable.
Consider the following fluoromethylpentene:
The proper name for this molecule is either trans-2-fluoro-3-methylpent-2-ene because
the alkyl groups that form the backbone chain reside across the double bond from each other,
or-2-fluoro-3-methylpent-2-ene because the highest-priority groups on each side of the
double bond are on the same side of the double bond.
Fluoro is the highest-priority group on the left side of the double bond, and ethyl is
the highest-priority group on the right side of the molecule.
The terms cis and trans are also used to describe the relative position of two substituents
on a ring; cis if on the same side, otherwise trans.
Conformers
Conformational isomerism is a form of isomerism that describes the phenomenon of molecules
with the same structural formula but with different shapes due to rotations about one
or more bonds.
Different conformations can have different energies, can usually interconvert, and are
very rarely isolatable.
For example, cyclohexane can exist in a variety of different conformations including a chair
conformation and a boat conformation, but, for cyclohexane itself, these can never be
separated.
The boat conformation represents the energy maximum on a conformational itinerary between
the two equivalent chair forms; however, it does not represent the transition state for
this process, because there are lower-energy pathways.
There are some molecules that can be isolated in several conformations, due to the large
energy barriers between different conformations. 2,2,2',2'-Tetrasubstituted biphenyls can fit
into this latter category.
Atropisomers
Atropisomers are stereoisomers resulting from hindered rotation about single bonds where
the steric strain barrier to rotation is high enough to allow for the isolation of the conformers.
More definitions A configurational stereoisomer is a stereoisomer
of a reference molecule that has the opposite configuration at a stereocenter.
This means that configurational isomers can be interconverted only by breaking covalent
bonds to the stereocenter, for example, by inverting the configurations of some or all
of the stereocenters in a compound.
Le Bel-van't Hoff rule Le Bel-van't Hoff rule states that if n is
the number of asymmetric carbon atoms then the maximum number of isomers = 2n.
As an example, the aldohexose D-glucose has the formula 6, of which four of its six carbons
atoms are stereogenic or asymmetric, making it one of 24=16 possible stereoisomers.
References