-
compound or meso
isomer is an
optically inactive isomer in a set of stereoisomers, at
least two of
which are
optically active. This
means that despite...
- conversion, by heat or by
chemical reaction, of an
optically active compound into a
racemic (
optically inactive) form. This
creates a 1:1
molar ratio of enantiomers...
-
While carbons 1 and 5 are
asymmetric carbons,
tropane itself is
optically inactive due to
mirror symmetry. 8-Azabicyclo[3.2.1]octane (tropane without...
- to
fading upon
prolonged exposure to UV, due to the
formation of
optically inactive cis-stilbenes. They are also
degraded by
oxygen in air, like most...
- name for an
optically inactive or
racemic form of
tartaric acid. It is an
equal mixture of two mirror-image
isomers (enantiomers),
optically active in opposing...
-
insoluble in cold water. Due to the
symmetry in the molecule, it is
optically inactive even
though it has
chiral carbon atoms (i.e., it is a meso compound)...
- When
seeded appropriated,
saturated solutions of this salt (which is
optically inactive), will
produce batches of
single enantiomeric crystals. An
early example...
- instead. The
usage of d and l is
discouraged by IUPAC. A
racemate is
optically inactive (achiral),
meaning that such
materials do not
rotate the polarization...
- zero
degrees are
called '
optically inactive'
chemicals and like water, they do not need to be
considered when
calculating optical rotation,
outside of the...
- is why
racemates are
optically inactive, as they
nullify their clockwise and
counter clockwise optical activities. The
optical rotation is proportional...
