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  2. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    Number of isomers [3] [4] Number of isomers including stereoisomers [3] [5] Molecular Formula Name of straight chain Synonyms 1 1 1 CH 4: methane: methyl hydride; natural gas 2 1 1 C 2 H 6: ethane: dimethyl; ethyl hydride; methyl methane 3 1 1 C 3 H 8: propane: dimethyl methane; propyl hydride 4 2 2 C 4 H 10: n-butane: butyl hydride ...

  3. Cahn–Ingold–Prelog priority rules - Wikipedia

    en.wikipedia.org/wiki/Cahn–Ingold–Prelog...

    A molecule may contain any number of stereocenters and any number of double bonds, and each usually gives rise to two possible isomers. A molecule with an integer n describing the number of stereocenters will usually have 2 n stereoisomers , and 2 n −1 diastereomers each having an associated pair of enantiomers .

  4. C3H6O2 - Wikipedia

    en.wikipedia.org/wiki/C3H6O2

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  5. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    Discounting isomers that are equivalent under rotations, there are nine isomers that differ by this criterion, and behave as different stable substances (two of them being enantiomers of each other). The most common one in nature ( myo -inositol) has the hydroxyls on carbons 1, 2, 3 and 5 on the same side of that plane, and can therefore be ...

  6. Octane - Wikipedia

    en.wikipedia.org/wiki/Octane

    Octane has many structural isomers that differ by the location of branching in the carbon chain. One of these isomers, 2,2,4-trimethylpentane (commonly called iso-octane), is used as one of the standard values in the octane rating scale. Octane is a component of gasoline and petroleum.

  7. 1,2,3,4-Cyclohexanetetrol - Wikipedia

    en.wikipedia.org/wiki/1,2,3,4-Cyclohexanetetrol

    The previous route was reduction of the peroxide brige to yield 3α,6α-dihydroxy cyclohexene, followed by di-hydoxylation of the double bond; which yielded a mixture of the 1,4/2,3 and 1,2,3,4/0 isomers. The authors found that, by reversing the order of the two steps, they could obtain 1,4/2,3 in 80% yield. [9] [10] [11]

  8. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    Functional isomers are structural isomers which have different functional groups, resulting in significantly different chemical and physical properties. [ 11 ] An example is the pair propanal H 3 C–CH 2 –C(=O)-H and acetone H 3 C–C(=O)–CH 3 : the first has a –C(=O)H functional group, which makes it an aldehyde , whereas the second has ...

  9. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    Cis–trans isomers are stereoisomers, that is, pairs of molecules which have the same formula but whose functional groups are in different orientations in three-dimensional space. Cis and trans isomers occur both in organic molecules and in inorganic coordination complexes.