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  2. Chirality - Wikipedia

    en.wikipedia.org/wiki/Chirality

    Macroscopic examples of chirality are found in the plant kingdom, the animal kingdom and all other groups of organisms. A simple example is the coiling direction of any climber plant, which can grow to form either a left- or right-handed helix. In anatomy, chirality is found in the imperfect mirror image symmetry of many kinds of animal bodies.

  3. Helicene - Wikipedia

    en.wikipedia.org/wiki/Helicene

    The systematic naming for this class of compounds is based on the number of rings: [n]helicene is the structure consisting of n rings. According to IUPAC, only structures where n is at least 5 are considered helicenes. [1] Some specific compounds also have alternate or trivial names.

  4. 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.

  5. Rule of mutual exclusion - Wikipedia

    en.wikipedia.org/wiki/Rule_of_mutual_exclusion

    The rule of mutual exclusion in molecular spectroscopy relates the observation of molecular vibrations to molecular symmetry.It states that no normal modes can be both Infrared and Raman active in a molecule that possesses a center of symmetry.

  6. Helicity basis - Wikipedia

    en.wikipedia.org/wiki/Helicity_basis

    The two-component helicity eigenstates satisfy ^ (^) = (^) where are the Pauli matrices, ^ is the direction of the fermion momentum, = depending on whether spin is pointing in the same direction as ^ or opposite.

  7. Chirality (physics) - Wikipedia

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

    Since the helicity of massive particles is frame-dependent, it might seem that the same particle would interact with the weak force according to one frame of reference, but not another. The resolution to this paradox is that the chirality operator is equivalent to helicity for massless fields only, for which helicity is not frame-dependent. By ...

  8. Metamerism (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Metamerism_(Chemistry)

    In chemistry, metamerism is used to define the isomeric relationship between compounds with the same polyvalent, heteroatomic, functional group but differ in the main carbon chain or any of the side chains. It has rather been an obsolete term for isomerism, which has not been recognised by IUPAC in its publications. [1]

  9. National Standard Examination in Chemistry - Wikipedia

    en.wikipedia.org/wiki/National_Standard...

    The National Standard Examination in Chemistry or NSEC is an examination in chemistry for higher secondary school students in India, usually conducted in the end of November. [1] The examination is organized by the Indian Association of Chemistry Teachers. Over 30,000 students, mainly from Standard 12, sit for this examination.