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Chirality

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right- and left-hand traffic
directionality of traffic flow, varies by national traffic laws
tartaric acid
C4-organic acid with different stereoisomers
thalidomide
Thalidomide, sold under the brand names Contergan, Distaval and Thalomid among others, is an oral administered medication used to treat a number of cancers (e.g., multiple myeloma), graft-versus-host disease, and many skin disorders (e.g., complications of leprosy such as skin lesions). Thalidomide has been used to treat conditions associated with HIV: aphthous ulcers, HIV-associated wasting syndrome, diarrhea, and Kaposi's sarcoma, but increases in HIV viral load have been reported.
chirality
geometric property of some molecules and ions
handedness
thumb|Stenciled hands at the Cueva de las Manos in Argentina. Left hands make up over 90% of the artwork, demonstrating the prevalence of right-handedness. thumb|A schoolgirl writing with her left hand In human biology, handedness is an individual's preferential use of one hand, known as the dominant hand, due to and causing it to be stronger, faster or more dextrous. The other hand, comparatively often the weaker, less dextrous or simply less subjectively preferred, is called the non-dominant hand. In a study from 1975 on 7,688 children in US grades 1–6, left handers comprised 9.6% of the sam
mefloquine
Mefloquine, sold under the brand name Lariam among others, is a medication used to prevent or treat malaria. When used for prevention it is typically started before potential exposure and continued for several weeks after potential exposure. It can be used to treat mild or moderate malaria but is not recommended for severe malaria. It is taken by mouth.
mirror image
(in a plane mirror) reflected duplication of an object that appears almost identical, but is reversed in the direction perpendicular to the mirror surface
Harold Scott MacDonald Coxeter
Canadian mathematician (1907–2003)
laterality
thumb|Left hemisphere of a human brain The term laterality refers to asymmetric preference, usage, skill, or specialization of symmetric body parts in an organism. Humans exhibit laterality in many ways, including limb dominance such as left and right handedness and footedness as well as specialization of one brain hemisphere over the other for certain functions such as language. Many other animals have also been shown to exhibit laterality in their own ways.
chirality
phenomenon applied in physics
chirality
geometric property of an object which cannot be mapped to its mirror image by rotations and translations alone
chirality
thumb|Two enantiomers of a generic amino acid that is chiral
bromochlorofluoroiodomethane
Bromochlorofluoroiodomethane is a hypothetical haloalkane with all four stable halogen substituents present in it.
racemic acid
racemic mixture of tartaric acid
homochirality
Homochirality is a uniformity of chirality, or handedness. Objects are chiral when they cannot be superposed on their mirror images. For example, the left and right hands of a human are approximately mirror images of each other but are not their own mirror images, so they are chiral. In chemistry, chirality is a geometric property of some compounds and ions. These compounds exist in two different chiral conformations, enantiomers, often described as the left-handed and right-handed isomers of a compound (denoted by L- (levorotatory to the left) and D- (dextrorotatory to the right), respectivel
mirror life
hypothetical form of life with mirror-reflected molecular building blocks (proteins, nucleic acids, etc.)
planar chirality
special case of chirality for two dimensions
optical rotatory dispersion
method of measuring the dispersion of an optically active molecule to determine the relative magnitude of right- or left-handed components, and some structural features of the molecule
sinistral and dextral
two types of chirality
bromochlorofluoromethane
Bromochlorofluoromethane or fluorochlorobromomethane, is a chemical compound and trihalomethane derivative with the chemical formula . As one of the simplest possible stable chiral compounds, it is useful for fundamental research into this area of chemistry. However, its relative instability to hydrolysis, and lack of suitable functional groups, made separation of the enantiomers of bromochlorofluoromethane especially challenging, and this was not accomplished until almost a century after it was first synthesised, in March 2005, though it has now been done by a variety of methods. More recent
Chiral polytope