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  2. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    Alkynes are capable of adding two equivalents of H 2, whereas an alkene adds only one equivalent. [11] Depending on catalysts and conditions, alkynes add one or two equivalents of hydrogen. Partial hydrogenation , stopping after the addition of only one equivalent to give the alkene , is usually more desirable since alkanes are less useful:

  3. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    Alkenes generally have stronger smells than their corresponding alkanes. Ethylene has a sweet and musty odor. Strained alkenes, in particular, like norbornene and trans -cyclooctene are known to have strong, unpleasant odors, a fact consistent with the stronger π complexes they form with metal ions including copper.

  4. Alkane - Wikipedia

    en.wikipedia.org/wiki/Alkane

    A straight-chain alkane will have a boiling point higher than a branched-chain alkane due to the greater surface area in contact, and thus greater van der Waals forces, between adjacent molecules. For example, compare isobutane (2-methylpropane) and n-butane (butane), which boil at −12 and 0 °C, and 2,2-dimethylbutane and 2,3-dimethylbutane ...

  5. Hydrocarbon - Wikipedia

    en.wikipedia.org/wiki/Hydrocarbon

    Unsaturated hydrocarbons, which have one or more double or triple bonds between carbon atoms. Those with one or more double bonds are called alkenes. Those with one double bond have the formula C n H 2n (assuming non-cyclic structures). [1]: 628 Those containing triple bonds are called alkyne. Those with one triple bond have the formula C n H ...

  6. Saturated and unsaturated compounds - Wikipedia

    en.wikipedia.org/wiki/Saturated_and_unsaturated...

    alkene (unsaturated) vs alkane (saturated) alkyne (unsaturated) vs alkane (saturated) arene (unsaturated) vs cycloalkane (saturated) For organic compounds containing heteroatoms (other than C and H), the list of unsaturated groups is long but some common types are:

  7. Reductions with diimide - Wikipedia

    en.wikipedia.org/wiki/Reductions_with_diimide

    Trans alkenes react more rapidly than cis alkenes in general. The reactivity difference between alkynes and alkenes is usually not great enough to isolate intermediate alkenes; however, alkenes can be isolated from allene reductions. Diimide reduces symmetrical double bonds i.e., C=C. N=N, O=O etc. unsymmetrical double bonds can not be reduced

  8. 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

  9. Carbon–hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond

    Because of this small difference in electronegativities, the C−H bond is generally regarded as being non-polar. In structural formulas of molecules, the hydrogen atoms are often omitted. Compound classes consisting solely of C−H bonds and C−C bonds are alkanes, alkenes, alkynes, and aromatic hydrocarbons.