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  2. Glyceraldehyde - Wikipedia

    en.wikipedia.org/wiki/Glyceraldehyde

    Glyceraldehyde has one chiral center and therefore exists as two different enantiomers with opposite optical rotation: . In the D/L nomenclature, either D from Latin Dexter meaning "right", or L from Latin Laevo meaning "left"

  3. Stereocenter - Wikipedia

    en.wikipedia.org/wiki/Stereocenter

    In stereochemistry, a stereocenter of a molecule is an atom (center), axis or plane that is the focus of stereoisomerism; that is, when having at least three different groups bound to the stereocenter, interchanging any two different groups creates a new stereoisomer. [1] [2] Stereocenters are also referred to as stereogenic centers.

  4. Racemic mixture - Wikipedia

    en.wikipedia.org/wiki/Racemic_mixture

    A racemic mixture is denoted by the prefix (±)-or dl-(for sugars the prefix dl-may be used), indicating an equal (1:1) mixture of dextro and levo isomers. Also the prefix rac- (or racem- ) or the symbols RS and SR (all in italic letters) are used.

  5. Chiral drugs - Wikipedia

    en.wikipedia.org/wiki/Chiral_drugs

    In this approach: identify the chiral center, label the four atoms directly attached to the stereogenic center in question, assign priorities according to the sequence rule ( from 1 to 4), rotate the molecule until the lowest priority (number 4) substituent is away from the observer/viewer, draw a curve from number 1 to number 2 to number 3 ...

  6. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    There are three common naming conventions for specifying one of the two enantiomers (the absolute configuration) of a given chiral molecule: the R/S system is based on the geometry of the molecule; the (+)- and (−)- system (also written using the obsolete equivalents d- and l-) is based on its optical rotation properties; and the D/L system is based on the molecule's relationship to ...

  7. Chirality (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Chirality_(chemistry)

    An example of a molecule that does not have a mirror plane or an inversion and yet would be considered achiral is 1,1-difluoro-2,2-dichlorocyclohexane (or 1,1-difluoro-3,3-dichlorocyclohexane). This may exist in many conformers ( conformational isomers ), but none of them has a mirror plane.

  8. Today's Wordle Hint, Answer for #1260 on Saturday, November ...

    www.aol.com/todays-wordle-hint-answer-1260...

    Today's Wordle Answer for #1260 on Saturday, November 30, 2024. Today's Wordle answer on Saturday, November 30, 2024, is DOGMA. How'd you do? Next: Catch up on other Wordle answers from this week.

  9. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    Absolute configuration showing the determination of the R and S descriptors. In chemistry, absolute configuration refers to the spatial arrangement of atoms within a molecular entity (or group) that is chiral, and its resultant stereochemical description. [1]