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In stereochemistry, prochiral molecules are those that can be converted from achiral to chiral in a single step. [1] [2] An achiral species which can be converted to a chiral in two steps is called proprochiral. [2] If two identical substituents are attached to an sp 3-hybridized atom, the descriptors pro-R and pro-S are used to distinguish ...
Instead, both effects can also occur when the propagation direction of the electromagnetic wave together with the structure of an (achiral) material form a chiral experimental arrangement. [10] [11] This case, where the mutual arrangement of achiral components forms a chiral (experimental) arrangement, is known as extrinsic chirality. [12] [13]
The simplest chiral knot is the trefoil knot, which was shown to be chiral by Max Dehn. All nontrivial torus knots are chiral. The Alexander polynomial cannot distinguish a knot from its mirror image, but the Jones polynomial can in some cases; if V k ( q ) ≠ V k ( q −1 ), then the knot is chiral, however the converse is not true.
An achiral molecule having chiral conformations could theoretically form a mixture of right-handed and left-handed crystals, as often happens with racemic mixtures of chiral molecules (see Chiral resolution#Spontaneous resolution and related specialized techniques), or as when achiral liquid silicon dioxide is cooled to the point of becoming ...
Any planar pattern that does not have a line of mirror symmetry is 2d-chiral, and examples include flat spirals and letters such as S, G, P. In contrast to 3d-chiral objects, the perceived sense of twist of 2d-chiral patterns is reversed for opposite directions of observation.
In this approach, an enantiomerically pure compound, the chiral selector, is added to the mobile phase and separation happens on a conventional achiral column. When a mixture of enantiomers is introduced into the chromatographic system, the individual enantiomers form transient diastereomeric complexes with the chiral mobile phase additive.
In stereochemistry, a chiral auxiliary is a stereogenic group or unit that is temporarily incorporated into an organic compound in order to control the stereochemical outcome of the synthesis. [ 1 ] [ 2 ] The chirality present in the auxiliary can bias the stereoselectivity of one or more subsequent reactions.
A scalar field model encoding chiral symmetry and its breaking is the chiral model. The most common application is expressed as equal treatment of clockwise and counter-clockwise rotations from a fixed frame of reference. The general principle is often referred to by the name chiral symmetry.