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  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. Chiral column chromatography - Wikipedia

    en.wikipedia.org/wiki/Chiral_column_chromatography

    The chiral stationary phase, CSP, can interact differently with two enantiomers, by a process known as chiral recognition. Chiral recognition depends on various interactions such as hydrogen bonding, π-π interaction, dipole stacking, inclusion complexation, steric, hydrophobic and electrostatic interaction, charge-transfer interactions, ionic interactions etc, between the analyte and the CSP ...

  4. 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.

  5. 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]

  6. 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]

  7. Why Does Lettuce Turn Pink After Being Cut—and Is It Safe to Eat?

    www.aol.com/why-does-lettuce-turn-pink-110800375...

    Here at BHG, we love to make Popeye proud by getting our Rx of greens.When we have the time, we toss together a main dish salad from scratch, but we’re also not too proud to admit that we rely ...

  8. What causes whiteheads? Explaining your acne issues - AOL

    www.aol.com/causes-whiteheads-explaining-acne...

    Adapalene is the one retinoid you can buy without a prescription, the AAD notes. Salicylic acid , which exfoliates the skin's surface and helps to remove oil from pores.

  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.