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  2. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    In chemistry, isomers are molecules or polyatomic ions with identical molecular formula – that is, the same number of atoms of each element – but distinct arrangements of atoms in space. [1] Isomerism refers to the existence or possibility of isomers. Isomers do not necessarily share similar chemical or physical properties.

  3. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    In one isomer the CO ligands are terminal. When a pair of CO are bridging, cis and trans isomers are possible depending on the location of the C 5 H 5 groups. [7] Another example in organometallic chemistry is the linkage isomerization of decaphenylferrocene, [(η 5-C 5 Ph 5) 2 Fe]. [8] [9] Formation of decaphenylferrocene from its linkage isomer

  4. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    The question of whether steric hindrance is responsible for the eclipsed energy maximum is a topic of debate to this day. One alternative to the steric hindrance explanation is based on hyperconjugation as analyzed within the Natural Bond Orbital framework.

  5. Isomerase - Wikipedia

    en.wikipedia.org/wiki/Isomerase

    Isomers themselves exist in many varieties but can generally be classified as structural isomers or stereoisomers. Structural isomers have a different ordering of bonds and/or different bond connectivity from one another, as in the case of hexane and its four other isomeric forms ( 2-methylpentane , 3-methylpentane , 2,2-dimethylbutane , and 2 ...

  6. Stereochemistry - Wikipedia

    en.wikipedia.org/wiki/Stereochemistry

    Stereochemistry, a subdiscipline of chemistry, studies the spatial arrangement of atoms that form the structure of molecules and their manipulation. [1] The study of stereochemistry focuses on the relationships between stereoisomers, which are defined as having the same molecular formula and sequence of bonded atoms (constitution) but differing in the geometric positioning of the atoms in space.

  7. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    A skeletal isomer of a compound is a structural isomer that differs from it in the atoms and bonds that are considered to comprise the "skeleton" of the molecule. For organic compounds, such as alkanes, that usually means the carbon atoms and the bonds between them.

  8. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    Two kinds of stereoisomers. In stereochemistry, stereoisomerism, or spatial isomerism, is a form of isomerism in which molecules have the same molecular formula and sequence of bonded atoms (constitution), but differ in the three-dimensional orientations of their atoms in space.

  9. Nuclear isomer - Wikipedia

    en.wikipedia.org/wiki/Nuclear_isomer

    A nuclear isomer is a metastable state of an atomic nucleus, in which one or more nucleons (protons or neutrons) occupy excited state levels (higher energy levels). ). "Metastable" describes nuclei whose excited states have half-lives 100 to 1000 times longer than the half-lives of the excited nuclear states that decay with a "prompt" half life (ordinarily on the order of 10