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  2. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    The following is a list of straight-chain alkanes, the total number of isomers of each (including branched chains), and their common names, sorted by number of carbon atoms. [ 1 ] [ 2 ] Number of C atoms

  3. Hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Hydrocarbon

    Hydrocarbons with the same molecular formula but different structural formulae are called structural isomers. [1]: 625 As given in the example of 3-methylhexane and its higher homologues, branched hydrocarbons can be chiral. [1]: 627 Chiral saturated hydrocarbons constitute the side chains of biomolecules such as chlorophyll and tocopherol. [3]

  4. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    Number and name the side chains before the name of the root chain; If there are multiple side chains of the same type, use prefixes such as "di-" and "tri-" to indicate it as such, and number each one. Add side chain names in alphabetical (disregarding "di-" etc. prefixes) order in front of the name of the root chain

  5. Methylene group - Wikipedia

    en.wikipedia.org/wiki/Methylene_group

    The group may be represented as −CH 2 − or >CH 2, where the '>' denotes the two bonds. This stands in contrast to a situation where the carbon atom is bound to the rest of the molecule by a double bond, which is preferably called a methylidene group, represented =CH 2. [2] Formerly the methylene name was used for both isomers.

  6. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Aliphatic compounds can be saturated, joined by single bonds (), or unsaturated, with double bonds or triple bonds ().If other elements (heteroatoms) are bound to the carbon chain, the most common being oxygen, nitrogen, sulfur, and chlorine, it is no longer a hydrocarbon, and therefore no longer an aliphatic compound.

  7. Double bond - Wikipedia

    en.wikipedia.org/wiki/Double_bond

    These effects become more pronounced for the heavier elements. The distannene (Me 3 Si) 2 CHSn=SnCH(SiMe 3) 2 has a tin-tin bond length just a little shorter than a single bond, a trans bent structure with pyramidal coordination at each tin atom, and readily dissociates in solution to form (Me 3 Si) 2 CHSn: (stannanediyl, a carbene analog). The ...

  8. Side chain - Wikipedia

    en.wikipedia.org/wiki/Side_chain

    The side chain is a hydrocarbon branching element of a molecule that is attached to a larger hydrocarbon backbone. It is one factor in determining a molecule's properties and reactivity. [2] A side chain is also known as a pendant chain, but a pendant group (side group) has a different definition.

  9. Hexene - Wikipedia

    en.wikipedia.org/wiki/Hexene

    In organic chemistry, hexene is a hydrocarbon with the chemical formula C 6 H 12.The prefix "hex" is derived from the fact that there are 6 carbon atoms in the molecule, while the "-ene" suffix denotes that there is an alkene present—two carbon atoms are connected via a double bond.