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  2. List of straight-chain alkanes - Wikipedia

    en.wikipedia.org/wiki/List_of_straight-chain_alkanes

    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; methylethyl methane 5 3 3 C 5 H 12: n-pentane: amyl hydride; Skellysolve A 6 5 5 C 6 H ...

  3. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.

  4. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For example, the simplest alkane is CH 4 methane, and the nine-carbon alkane CH 3 (CH 2) 7 CH 3 is named nonane. The names of the first four alkanes were derived from methanol, ether, propionic acid and butyric acid, respectively.

  5. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    However, the chain of carbon atoms may also be branched at one or more points. The number of possible isomers increases rapidly with the number of carbon atoms. For example, for acyclic alkanes: [3] C 1: methane only; C 2: ethane only; C 3: propane only; C 4: 2 isomers: butane and isobutane; C 5: 3 isomers: pentane, isopentane, and neopentane

  6. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Formula Name Structural formula Chemical classification CH 4: Methane: Alkane C 2 H 2: Acetylene: Alkyne C 2 H 4: Ethylene: Alkene C 2 H 6: Ethane: Alkane C 3 H 4: Propyne: Alkyne C 3 H 6: Propene: Alkene C 3 H 8: Propane: Alkane C 4 H 6: 1,2-Butadiene: Diene: C 4 H 6: 1-Butyne: Alkyne C 4 H 8: 1-Butene: Alkene C 4 H 10: Butane: Alkane C 6 H 10 ...

  7. Carboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Carboxylic_acid

    For example, at room temperature, in a 1-molar solution of acetic acid, only 0.001% of the acid are dissociated (i.e. 10 −5 moles out of 1 mol). Electron-withdrawing substituents, such as -CF 3 group , give stronger acids (the p K a of acetic acid is 4.76 whereas trifluoroacetic acid, with a trifluoromethyl substituent , has a p K a of 0.23).

  8. Hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Hydrocarbon

    Methane is part of a homologous series known as the alkanes, which contain single bonds only. In organic chemistry, a hydrocarbon is an organic compound consisting entirely of hydrogen and carbon. [1]: 620 Hydrocarbons are examples of group 14 hydrides.

  9. Tetracosane - Wikipedia

    en.wikipedia.org/wiki/Tetracosane

    Tetracosane, also called tetrakosane, is an alkane hydrocarbon with the structural formula H(CH 2) 24 H. As with other alkanes, its name is derived from Greek for the number of carbon atoms, 24, in the molecule. It has 14,490,245 constitutional isomers, [2] and 252,260,276 stereoisomers. [3]