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  2. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    In acetylene, the H–C≡C bond angles are 180°. By virtue of this bond angle, alkynes are rod-like. Correspondingly, cyclic alkynes are rare. Benzyne cannot be isolated. . The C≡C bond distance of 118 picometers (for C 2 H 2) is much shorter than the C=C distance in alkenes (132 pm, for C 2 H 4) or the C–C bond in alkanes (153 p

  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

    In organic chemistry, an alkane, or paraffin (a historical trivial name that also has other meanings), is an acyclic saturated hydrocarbon. In other words, an alkane consists of hydrogen and carbon atoms arranged in a tree structure in which all the carbon–carbon bonds are single. [1] Alkanes have the general chemical formula C n H 2n+2.

  5. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    n-, iso- and cyclo-alkanes (saturated hydrocarbons) n-, iso- and cyclo-alkenes and -alkynes (unsaturated hydrocarbons). Important examples of low-molecular aliphatic compounds can be found in the list below (sorted by the number of carbon-atoms):

  6. Cycloalkene - Wikipedia

    en.wikipedia.org/wiki/Cycloalkene

    This is because the bond angle for an alkene, C-C=C, is 122°, while the bond angle for an alkane, C-C-C, is 112°. When these carbons form a small ring, the alkene which has a larger bond angle will have to compress more than the alkane causing more bond angle strain. [4] Cycloalkenes have a lower melting point than cycloalkanes of the same size.

  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. 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.

  9. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    In organic chemistry, syn-and anti-addition are different ways in which substituent molecules can be added to an alkene (R 2 C=CR 2) or alkyne (RC≡CR).The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction.