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  Alkynes are hydrocarbons that have at least one triple bond between two carbon atoms, with the formula CnH2n-2. The alkynes are traditionally known as acetylenes or the acetylene series, although the name acetylene is also used to refer specifically to the simplest member of the series, known as ethyne (C2H2) using formal IUPAC nomenclature.


Chemical properties

Unlike alkanes, and to a lesser extent, alkenes, alkynes are unstable and reactive. Terminal alkynes and acetylene are fairly acidic and have pKa values (25) between that of ammonia (35) and ethanol (16). This acidity is due to the ability for the negative charge in the acetylide conjugate base to be stabilized as a result of the high s character of the sp orbital, in which the electron pair resides. Electrons in an s orbital benefit from closer proximity to the positively charged atom nucleus, and are therefore lower in energy. This can also be thought of in terms of electronegativity: electrons in an hybrid orbital with high s character reside closer to the nucleus. The closer proximity of the electrons to the nucleus allows an acetylinic carbon to have a greater amount of electronegative character. As a result, a proton is more easily removed from the carbon as electrons flow more willingly to a more electronegative atom.

A terminal alkyne with a strong base such as sodium, sodium amide, n-butyllithium or a Grignard reagent, gives the anion of the terminal alkyne (a metal acetylide):

2 RC≡CH + 2 Na → 2 RC≡CNa + H2

More generally:

RC≡CH + B → RC≡C + HB+, where B denotes a strong base.

The acetylide anion is synthetically useful because as a strong nucleophile, it can participate in C−C bond forming reactions.

It is also possible to form copper and silver alkynes, from this group of compounds silver acetylide is an often used example.

See also: Metal acetylide


The carbon atoms in an alkyne bond are sp hybridized: they each have 2 p orbitals and 2 sp hybrid orbitals. Overlap of an sp orbital from each atom forms one sp-sp sigma bond. Each p orbital on one atom overlaps one on the other atom, forming two pi bonds, giving a total of three bonds. The remaining sp orbital on each atom can form a sigma bond to another atom, for example to hydrogen atoms in the parent compound acetylene. The two sp orbitals on an atom are on opposite sides of the atom: in acetylene, the H-C-C bond angles are 180°. Because a total of 6 electrons take part in bonding this triple bond is very strong with a bond strength of 839 kJ/mol. The sigma bond contributes 369 kJ/mol, the first pi bond contributes 268 kJ/mol and the second pi bond is weak with 202 kJ/mol bond strength. The CC bond distance with 121 picometers is also much less than that of the alkene bond which is 134 pm or the alkane bond with 153 pm.

The simplest alkyne is ethyne (acetylene): H-C≡C-H

Terminal and internal alkynes

Terminal alkynes have a hydrogen atom bonded to at least one of the sp hybridized carbons (those involved in the triple bond. An example would be methylacetylene (1-propyne using IUPAC nomenclature).


Internal alkynes have something other than hydrogen attached to the sp hybridized carbons, usually another carbon atom, but could be a heteroatom. A good example is 2-pentyne, in which there is a methyl group on one side of the triple bond and an ethyl group on the other side.



Alkynes are generally prepared by dehydrohalogenation of vicinal alkyl dihalides or the reaction of metal acetylides with primary alkyl halides. In the Fritsch-Buttenberg-Wiechell rearrangement an alkyne is prepared starting from a vinyl bromide.

Alkynes can be prepared from aldehydes using the Corey-Fuchs reaction and from aldehydes or ketones by the Seyferth-Gilbert homologation.


Alkynes are involved in many organic reactions.


  1. ^ Fukuda, Y.; Utimoto, K. "Effective transformation of unactivated alkynes into ketones or acetals with a gold(III) catalyst". J. Org. Chem. 1991, 56, 3729–3731. doi:10.1021/jo00011a058
  2. ^ Mizushima, E.; Cui, D.-M.; Nath, D. C. D.; Hayashi, T.; Tanaka, M. "Au(I)-Catalyzed hydratation of alkynes: 2,8-nonanedione". Organic Syntheses, Vol. 83, p.55 (2005). Link.

Further reading

This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Alkyne". A list of authors is available in Wikipedia.
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