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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. 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

  4. 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]

  5. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Aliphatic compounds can be saturated (in which all the C-C bonds are single requiring the structure to be completed, or 'saturated', by hydrogen) like hexane, or unsaturated, like hexene and hexyne. Open-chain compounds, whether straight or branched, and which contain no rings of any type, are always aliphatic.

  6. Fluid catalytic cracking - Wikipedia

    en.wikipedia.org/wiki/Fluid_catalytic_cracking

    In the fluid catalytic cracking process, the HGO feedstock is heated to a high temperature and to a moderate pressure, and then is placed in contact with a hot, powdered catalyst, which breaks the long-chain molecules of the high-boiling-point hydrocarbon liquids into short-chain molecules, which then are collected as a vapor.

  7. Hydrocarbon plant - Wikipedia

    en.wikipedia.org/wiki/Hydrocarbon_plant

    The first form is a red algae that produces odd-numbered carbon chains roughly 25-31 atoms in length. [2] These carbon chains usually do not possess a large number of double bonds. The second type of B. braunii is green and produces even-numbered carbon chains that are between 34 and 38 carbons long, with many double bonds present. While the ...

  8. Glycerophospholipid - Wikipedia

    en.wikipedia.org/wiki/Glycerophospholipid

    These chains are branched, with one methyl substituent per C5 subunit. These chains are linked to the glycerol phosphate by ether linkages. [2] The two hydrocarbon chains attached to the glycerol are hydrophobic while the polar head, which mainly consists of the phosphate group attached to the third carbon of the glycerol backbone, is ...

  9. Straight-chain terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Straight-chain_terminal_alkene

    Straight-chain terminal alkenes, also called linear alpha olefins (LAO) or normal alpha olefins (NAO), are alkenes (olefins) having a chemical formula C n H 2n, distinguished from other alkenes with a similar molecular formula by being terminal alkenes, in which the double bond occurs at the alpha (α-, 1-or primary) position, and by having a linear (unbranched) hydrocarbon chain.