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Each crystallographic point group defines the (geometric) crystal class of the crystal. The point group of a crystal determines, among other things, the directional variation of physical properties that arise from its structure, including optical properties such as birefringency , or electro-optical features such as the Pockels effect .
It has reflection symmetry with respect to a plane perpendicular to the n-fold rotation axis. C nv, [n], (*nn) of order 2n - pyramidal symmetry or full acro-n-gonal group (abstract group Dih n); in biology C 2v is called biradial symmetry. For n=1 we have again C s (1*). It has vertical mirror planes. This is the symmetry group for a regular n ...
In chemistry, molecular symmetry describes the symmetry present in molecules and the classification of these molecules according to their symmetry. Molecular symmetry is a fundamental concept in chemistry, as it can be used to predict or explain many of a molecule's chemical properties , such as whether or not it has a dipole moment , as well ...
In structural biology, a protomer is the structural unit of an oligomeric protein. It is the smallest unit composed of at least one protein chain. The protomers associate to form a larger oligomer of two or more copies of this unit. Protomers usually arrange in cyclic symmetry to form closed point group symmetries.
When comparing the symmetry type of two objects, the origin is chosen for each separately, i.e., they need not have the same center. Moreover, two objects are considered to be of the same symmetry type if their symmetry groups are conjugate subgroups of O(3) (two subgroups H 1, H 2 of a group G are conjugate, if there exists g ∈ G such that H 1 = g −1 H 2 g).
According to the frontier molecular orbital theory, the sigma bond in the ring will open in such a way that the resulting p-orbitals will have the same symmetry as the HOMO of the product. [4] For the 5,6-dimethylcyclohexa-1,3-diene, only a disrotatory mode would result in p-orbitals having the same symmetry as the HOMO of hexatriene.
Thermolysis converts 1 to (E,E) geometric isomer 2, but 3 to (E,Z) isomer 4.. The Woodward–Hoffmann rules (or the pericyclic selection rules) [1] are a set of rules devised by Robert Burns Woodward and Roald Hoffmann to rationalize or predict certain aspects of the stereochemistry and activation energy of pericyclic reactions, an important class of reactions in organic chemistry.
Cyclic compounds may or may not exhibit aromaticity; benzene is an example of an aromatic cyclic compound, while cyclohexane is non-aromatic. In organic chemistry, the term aromaticity is used to describe a cyclic (ring-shaped), planar (flat) molecule that exhibits unusual stability as compared to other geometric or connective arrangements of ...