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The general structure of an ether. R and R' represent most organyl substituents.. In organic chemistry, ethers are a class of compounds that contain an ether group—a single oxygen atom bonded to two separate carbon atoms, each part of an organyl group (e.g., alkyl or aryl).
The etheric plane (see also etheric body) is a term introduced into Theosophy by Charles Webster Leadbeater and Annie Besant to represent the subtle part of the lower plane of existence. It represents the fourth [higher] subplane of the physical plane (a hyperplane), the lower three being the states of solid, liquid, and gaseous matter.
The etheric body, ether-body, or æther body is a subtle body propounded in esoteric and occult philosophies as the first or lowest layer in the human energy field or aura. [ 1 ] [ 2 ] The etheric body is said to be in immediate contact with the physical body and to sustain it and connect it with "higher" bodies.
In the 19th century, luminiferous aether (or ether), meaning light-bearing aether, was a theorized medium for the propagation of light. James Clerk Maxwell developed a model to explain electric and magnetic phenomena using the aether, a model that led to what are now called Maxwell's equations and the understanding that light is an ...
A Fischer projection can be used to differentiate between L- and D- molecules Chirality (chemistry). For instance, by definition, in a Fischer projection the penultimate carbon of D-sugars are depicted with hydrogen on the left and hydroxyl on the right. L-sugars will be shown with the hydrogen on the right and the hydroxyl on the left.
Luminiferous aether or ether [1] (luminiferous meaning 'light-bearing') was the postulated medium for the propagation of light. [2] It was invoked to explain the ability of the apparently wave-based light to propagate through empty space (a vacuum), something that waves should not be able to do. The assumption of a spatial plenum (space ...
For example, tartaric acid can exist as any of three stereoisomers depicted below in a Fischer projection. Of the four colored pictures at the top of the diagram , the first two represent the meso compound (the 2 R ,3 S and 2 S ,3 R isomers are equivalent), followed by the optically active pair of levotartaric acid (L-( R,R )-(+)-tartaric acid ...
Staggered conformation image right in Newman projection Eclipsed conformation. In organic chemistry, a staggered conformation is a chemical conformation of an ethane-like moiety abcX–Ydef in which the substituents a, b, and c are at the maximum distance from d, e, and f; this requires the torsion angles to be 60°. [1]