- not
rotate light.
Stereoisomers include both
enantiomers and diastereomers. Diastereomers, like
enantiomers,
share the same
molecular formula and are also...
-
mixture of the two
enantiomers in
equal parts is said to be racemic, and it
usually differs chemically and
physically from the pure
enantiomers.
Chiral molecules...
- (levorotatory) and
positive (+)
clockwise (dextrorotatory)
enantiomers. In
contrast to the two pure
enantiomers,
which have
identical physical properties except...
-
chiral molecule is dextrorotary, its
enantiomer (geometric
mirror image) will be laevorotary, and vice versa.
Enantiomers rotate plane-polarized
light the...
-
those that
contain equimolar amounts of both
enantiomers of a compound.
Racemate and
single enantiomer actions differ in most cases.
Absolute configuration...
- The two
enantiomers can be distinguished, for example, by the right-hand rule. This type of
isomerism is
called axial isomerism.
Enantiomers behave identically...
-
light and how they
interact with
different enantiomers of
other compounds. As a result,
different enantiomers of a
compound may have
substantially different...
-
compound by a
method that
favors the
formation of a
specific enantiomer or diastereomer.
Enantiomers are
stereoisomers that have
opposite configurations at...
-
racemic mixtures into
their respective enantiomers takes extra time, money, and energy. One way to
separate enantiomers is to
chemically convert them into...
-
Racemization occurs when one pure form of an
enantiomer is
converted into
equal proportion of both
enantiomers,
forming a racemate. When
there are both equal...
