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A dashed wedge indicates that the atom is behind the molecule; it is pointing below the plane of the paper. When a straight, un-dashed line is used, the atom is in the plane of the paper. This spatial arrangement provides an idea of the molecule in a 3-dimensional space and there are constraints as to how the spatial arrangements can be arranged.
In a hydrocarbon molecule with all carbon atoms making up the backbone in a tetrahedral molecular geometry, the zigzag backbone is in the paper plane (chemical bonds depicted as solid line segments) with the substituents either sticking out of the paper toward the viewer (chemical bonds depicted as solid wedges) or away from the viewer ...
The skeletal formula of the antidepressant drug escitalopram, featuring skeletal representations of heteroatoms, a triple bond, phenyl groups and stereochemistry. The skeletal formula, line-angle formula, bond-line formula or shorthand formula of an organic compound is a type of molecular structural formula that serves as a shorthand representation of a molecule's bonding and some details of ...
Fischer projection of D-Glyceraldehyde.Projection of a tetrahedral molecule onto a planar surface. Visualizing a Fischer projection. In chemistry, the Fischer projection, devised by Emil Fischer in 1891, is a two-dimensional representation of a three-dimensional organic molecule by projection.
A circular segment (in green) is enclosed between a secant/chord (the dashed line) and the arc whose endpoints equal the chord's (the arc shown above the green area). In geometry, a circular segment or disk segment (symbol: ⌓) is a region of a disk [1] which is "cut off" from the rest of the disk by a straight line.
[3] [4] This diagram style is an alternative to a sawhorse projection, which views a carbon–carbon bond from an oblique angle, or a wedge-and-dash style, such as a Natta projection. These other styles can indicate the bonding and stereochemistry, but not as much conformational detail.
Hofmann's 1865 ball-and-stick model of methane (CH 4).Later discoveries disproved this geometry. In 1865, German chemist August Wilhelm von Hofmann was the first to make ball-and-stick molecular models.
Square prismatic geometry (D 4h) is much less common compared to the square antiprism.An example of a molecular species with square prismatic geometry (a slightly flattened cube) is octafluoroprotactinate(V), [PaF 8] 3–, as found in its sodium salt, Na 3 PaF 8. [6]