When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Axial chirality - Wikipedia

    en.wikipedia.org/wiki/Axial_chirality

    Two types of molecules having axial chirality: allenes (left) and binaryl atropisomers (right) In chemistry, axial chirality is a special case of chirality in which a molecule contains two pairs of chemical groups in a non-planar arrangement about an axis of chirality so that the molecule is not superposable on its mirror image.

  3. Allenes - Wikipedia

    en.wikipedia.org/wiki/Allenes

    The two π-bonds are located at the 90° angle to each other, and thus require a reagent to approach from somewhat different directions. With an appropriate substitution pattern, allenes exhibit axial chirality as predicted by van’t Hoff as early as 1875. [64] [63] Protonation of allenes gives cations 11 that undergo further transformations. [65]

  4. Chirality - Wikipedia

    en.wikipedia.org/wiki/Chirality

    A chiral molecule is a type of molecule that has a non-superposable mirror image. The feature that is most often the cause of chirality in molecules is the presence of an asymmetric carbon atom. [16] [17] The term "chiral" in general is used to describe the object that is non-superposable on its mirror image. [18]

  5. Chirality (chemistry) - Wikipedia

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

    For a chiral molecule with one or more stereocenter, the enantiomer corresponds to the stereoisomer in which every stereocenter has the opposite configuration. An organic compound with only one stereogenic carbon is always chiral. On the other hand, an organic compound with multiple stereogenic carbons is typically, but not always, chiral.

  6. Chiral drugs - Wikipedia

    en.wikipedia.org/wiki/Chiral_drugs

    Optical purity is an obsolete term since today most of the chiral purity measurements are done using chromatographic techniques (not based on optical principles). Enantiomeric excess tells the extent (in %) to which the chiral substance contains one enantiomer over the other. For a racemic drug the enantiomeric excess will be 0%.

  7. 5 details you missed from the 'Saturday Night Live' 50th ...

    www.aol.com/5-details-missed-saturday-night...

    "SNL50: The Anniversary Special" aired on Sunday to celebrate 50 years of "Saturday Night Live." The star-studded event featured live performances, sketches, and references to current events.

  8. NYT ‘Connections’ Hints and Answers Today, Thursday, February 13

    www.aol.com/nyt-connections-hints-answers-today...

    Today's NYT Connections puzzle for Thursday, February 13, 2025The New York Times

  9. Chiral media - Wikipedia

    en.wikipedia.org/wiki/Chiral_media

    Chirality with hands and two enantiomers of a generic amino acid The direction of current flow and induced magnetic flux follow a "handness" relationship. The term chiral / ˈ k aɪ r əl / describes an object, especially a molecule, which has or produces a non-superposable mirror image of itself.