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  2. Pentane - Wikipedia

    en.wikipedia.org/wiki/Pentane

    Pentane is an organic compound with the formula C 5 H 12 —that is, an alkane with five carbon atoms. The term may refer to any of three structural isomers, or to a mixture of them: in the IUPAC nomenclature, however, pentane means exclusively the n-pentane isomer, in which case pentanes refers to a mixture of them; the other two are called isopentane (methylbutane) and neopentane ...

  3. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    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; C 6: 5 isomers: hexane, 2-methylpentane, 3-methylpentane, 2,2-dimethylbutane ...

  4. Isopentane - Wikipedia

    en.wikipedia.org/wiki/Isopentane

    It is one of three structural isomers with the molecular formula C 5 H 12, the others being pentane (n-pentane) and neopentane (2,2-dimethylpropane). Isopentane is commonly used in conjunction with liquid nitrogen to achieve a liquid bath temperature of −160 °C.

  5. Functional group - Wikipedia

    en.wikipedia.org/wiki/Functional_group

    In traditional names various qualifiers are used to label isomers, for example, isopropanol (IUPAC name: propan-2-ol) is an isomer of n-propanol (propan-1-ol). The term moiety has some overlap with the term "functional group". However, a moiety is an entire "half" of a molecule, which can be not only a single functional group, but also a larger ...

  6. 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.

  7. 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 ...

  8. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    The differences between cis and trans isomers can be larger if polar bonds are present, as in the 1,2-dichloroethenes. The cis isomer in this case has a boiling point of 60.3 °C, while the trans isomer has a boiling point of 47.5 °C. [ 6 ]

  9. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    When n is four or more, isomers are possible, distinguished by the position and conformation of the double bond. Alkenes are generally colorless non-polar compounds, somewhat similar to alkanes but more reactive. The first few members of the series are gases or liquids at room temperature.