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Axial loading is defined as applying a force on a structure directly along a given axis of said structure. [1] In the medical field, the term refers to the application of weight or force along the course of the long axis of the body. [2] The application of an axial load on the human spine can result in vertebral compression fractures. [3]
For example, sulfur hexafluoride (SF 6) is an octahedral molecule. Trigonal pyramidal : A trigonal pyramidal molecule has a pyramid-like shape with a triangular base. Unlike the linear and trigonal planar shapes but similar to the tetrahedral orientation, pyramidal shapes require three dimensions in order to fully separate the electrons.
An atom bonded to 5 other atoms (and no lone pairs) forms a trigonal bipyramid with two axial and three equatorial positions, but in the seesaw geometry one of the atoms is replaced by a lone pair of electrons, which is always in an equatorial position. This is true because the lone pair occupies more space near the central atom (A) than does a ...
Mesons named with the letter "f" are scalar mesons (as opposed to a pseudo-scalar meson), and mesons named with the letter "a" are axial-vector mesons (as opposed to an ordinary vector meson) a.k.a. an isoscalar vector meson, while the letters "b" and "h" refer to axial-vector mesons with positive parity, negative C-parity, and quantum numbers I G of 1 + and 0 − respectively.
[18]: 1165 Examples of this include the octacyanomolybdate (Mo(CN) 4− 8) and octafluorozirconate (ZrF 4− 8) anions. [18]: 1165 The nonahydridorhenate ion (ReH 2− 9) in potassium nonahydridorhenate is a rare example of a compound with a steric number of 9, which has a tricapped trigonal prismatic geometry. [13]: 254 [18]
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.
This meant a whole load of amendments and creating a whole W2 for the person who was missed. My client got us on a 3-way call where I inquired about that employee, and asked him to furnish his ...
The α- and β-anomers of D-glucopyranose.. In organic chemistry, the anomeric effect or Edward-Lemieux effect (after J. T. Edward and Raymond Lemieux) is a stereoelectronic effect that describes the tendency of heteroatomic substituents adjacent to a heteroatom within a cyclohexane ring to prefer the axial orientation instead of the less-hindered equatorial orientation that would be expected ...