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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]
A chiral compound can contain no improper axis of rotation (S n), which includes planes of symmetry and inversion center. Chiral molecules are always dissymmetric (lacking S n) but not always asymmetric (lacking all symmetry elements except the trivial identity). Asymmetric molecules are always chiral. [6]
A theory that is asymmetric with respect to chiralities is called a chiral theory, while a non-chiral (i.e., parity-symmetric) theory is sometimes called a vector theory. Many pieces of the Standard Model of physics are non-chiral, which is traceable to anomaly cancellation in chiral theories.
In stereochemistry, an asymmetric carbon is a carbon atom that is bonded to four different types of atoms or groups of atoms. [1] [2] The four atoms and/or groups attached to the carbon atom can be arranged in space in two different ways that are mirror images of each other, and which lead to so-called left-handed and right-handed versions (stereoisomers) of the same molecule.
Enantioselective synthesis, also called asymmetric synthesis, [1] is a form of chemical synthesis.It is defined by IUPAC as "a chemical reaction (or reaction sequence) in which one or more new elements of chirality are formed in a substrate molecule and which produces the stereoisomeric (enantiomeric or diastereomeric) products in unequal amounts."
The most obvious characteristic of flatfish, other than their flatness, is their asymmetric morphology: both eyes are on the same side of the head in the adult fish. In some families of flatfish, the eyes are always on the right side of the body ( dextral or right-eyed flatfish), and in others, they are always on the left ( sinistral or left ...
An object that is not chiral is said to be achiral. A chiral object and its mirror image are said to be enantiomorphs. The word chirality is derived from the Greek χείρ (cheir), the hand, the most familiar chiral object; the word enantiomorph stems from the Greek ἐναντίος (enantios) 'opposite' + μορφή (morphe) 'form'.
Axial chirality differs from central chirality (point chirality) in that axial chirality does not require a chiral center such as an asymmetric carbon atom, the most common form of chirality in organic compounds. Bonding to asymmetric carbon has the form Cabcd where a, b, c, and d must be distinct groups.