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  2. Fischer projection - Wikipedia

    en.wikipedia.org/wiki/Fischer_projection

    The use of Fischer projections in non-carbohydrates is discouraged, as such drawings are ambiguous and easily confused with other types of drawing. The main purpose of Fischer projections is to show the chirality of a molecule and to distinguish between a pair of enantiomers. Some notable uses include drawing sugars and depicting isomers. [1]

  3. Monosaccharide nomenclature - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide_nomenclature

    The Fischer projection is a systematic way of drawing the skeletal formula of an open-chain monosaccharide so that each stereoisomer is uniquely identified. Two isomers whose molecules are mirror-images of each other are identified by prefixes ' D-' or ' L-', according to the handedness of the chiral carbon atom that is farthest from the carbonyl.

  4. Valence isomer - Wikipedia

    en.wikipedia.org/wiki/Valence_isomer

    There are many valence isomers one can draw for the C 6 H 6 formula benzene. Some were originally proposed for benzene itself before the actual structure of benzene was known. Others were later synthesized in lab.

  5. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    In chemistry, isomers are molecules or polyatomic ions with identical molecular formula – that is, the same number of atoms of each element – but distinct arrangements of atoms in space. [1] Isomerism refers to the existence or possibility of isomers.

  6. Meso compound - Wikipedia

    en.wikipedia.org/wiki/Meso_compound

    One of the two meso isomers of 1,2,3,4-tetrafluorospiropentane, with S 4 symmetry. Since a meso isomer has a superposable mirror image, a compound with a total of n chiral centers cannot attain the theoretical maximum of 2 n stereoisomers if one of the stereoisomers is meso. [4] A meso isomer need not have a mirror plane.

  7. Stereochemistry - Wikipedia

    en.wikipedia.org/wiki/Stereochemistry

    Stereochemistry, a subdiscipline of chemistry, studies the spatial arrangement of atoms that form the structure of molecules and their manipulation. [1] The study of stereochemistry focuses on the relationships between stereoisomers, which are defined as having the same molecular formula and sequence of bonded atoms (constitution) but differing in the geometric positioning of the atoms in space.

  8. Taylor Kitsch Is Opening a Nature Retreat as a 'Tip of the ...

    www.aol.com/taylor-kitsch-opening-nature-retreat...

    Taylor Kitsch is honoring his sister Shelby Kitsch-Best in a special way.. In the mid-2010s, the Friday Night Lights alum, 43, took two years off of work to help Kitsch-Best through her addiction ...

  9. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    A simple example of cis–trans isomerism is the 1,2-disubstituted ethenes, like the dichloroethene (C 2 H 2 Cl 2) isomers shown below. [7] Dichloroethene isomers. Molecule I is cis-1,2-dichloroethene and molecule II is trans-1,2-dichloroethene.