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  2. 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]

  3. Chirality (chemistry) - Wikipedia

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

    A chiral substance is enantiopure when only one of two possible enantiomers is present so that all molecules within a sample have the same chirality sense. Use of homochiral as a synonym is strongly discouraged. [22] A chiral substance is enantioenriched or heterochiral when its enantiomeric ratio is greater than 50:50 but less than 100:0. [23]

  4. Chirality (physics) - Wikipedia

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

    A chiral phenomenon is one that is not identical to its mirror image (see the article on mathematical chirality).The spin of a particle may be used to define a handedness, or helicity, for that particle, which, in the case of a massless particle, is the same as chirality.

  5. 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.

  6. Chirality timeline - Wikipedia

    en.wikipedia.org/wiki/Chirality_timeline

    Chiral molecules in the receptors in our noses can tell the difference between these things. Chirality affects biochemical reactions, and the way a drug works depends on what kind of enantiomer it is. Many drugs are chiral and it is important that the shape of the drug matches the shape of the cell receptor it is meant to affect.

  7. 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 ...

  8. 30 Of The Weirdest Or Most Unfortunate Quora Posts - AOL

    www.aol.com/113-weirdest-questions-people-asked...

    Talking about the positives and negatives of Q&A websites and similar sources, Dr. Williams noted that, on the positive side, there’s access to unbiased experts who have knowledge and experience ...

  9. Chiral inversion - Wikipedia

    en.wikipedia.org/wiki/Chiral_inversion

    Chiral inversion is the process of conversion of one enantiomer of a chiral molecule to its mirror-image version with no other change in the molecule. [1] [2] [3] [4]Chiral inversion happens depending on various factors (viz. biological-, solvent-, light-, temperature- induced, etc.) and the energy barrier energy barrier associated with the stereogenic element present in the chiral molecule. 2 ...