Aliphatic compound






Acyclic aliphatic/non-aromatic compound (butane)



Cyclic aliphatic/non-aromatic compound (cyclobutane)


In organic chemistry, hydrocarbons (compounds composed of carbon and hydrogen) are divided into two classes: aromatic compounds and aliphatic compounds (/ˌælɪˈfætɪk/; G. aleiphar, fat, oil) also known as non-aromatic compounds. Aliphatics can be cyclic, but only aromatic compounds contain an especially stable ring of atoms, such as benzene.[1] Aliphatic compounds can be saturated, like hexane, or unsaturated, like hexene and hexyne. Open-chain compounds (whether straight or branched) contain no rings of any type, and are thus aliphatic.




Contents






  • 1 Structure


  • 2 Properties


  • 3 Examples of aliphatic compounds / non-aromatic


  • 4 References





Structure


Aliphatic compounds can be saturated, joined by single bonds (alkanes), or unsaturated, with double bonds (alkenes) or triple bonds (alkynes). Besides hydrogen, other elements can be bound to the carbon chain, the most common being oxygen, nitrogen, sulfur, and chlorine.


The least complex aliphatic compound is methane (CH4).



Properties


Most aliphatic compounds are flammable, allowing the use of hydrocarbons as fuel, such as methane in Bunsen burners and as liquefied natural gas (LNG), and acetylene in welding.



Examples of aliphatic compounds / non-aromatic


The most important aliphatic compounds are:



  • 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):

























































































































































Formula Name Structural Formula Chemical Classification
CH4
Methane Methane-2D-stereo.svg Alkane
C2H2
Acetylene Ethyne-2D-flat.png Alkyne
C2H4
Ethylene Ethene structural.svg Alkene
C2H6
Ethane Ethan Lewis.svg Alkane
C3H4
Propyne Propyne-2D-flat.png Alkyne
C3H6
Propene Propen21.PNG Alkene
C3H8
Propane Propane-2D-flat.png Alkane
C4H6
1,2-Butadiene Buta-1,2-dien.svg Diene
C4H6
1-Butyne Ethylacetylene.svg Alkyne
C4H8
1-Butene But-1-ene-2D-skeletal.png Alkene
C4H10
Butane Butane-2D-flat.png Alkane
C6H10
Cyclohexene Cyclohexen - Cyclohexene.svg Cycloalkene
C5H12

n-pentane
Pentan Skelett.svg Alkane
C7H14
Cycloheptane Cycloheptane.svg Cycloalkane
C7H14
Methylcyclohexane Methylcyclohexane.png Cyclohexane
C8H8
Cubane Cuban.svg Octane
C9H20
Nonane Nonan Skelett.svg Alkane
C10H12
Dicyclopentadiene Di-Cyclopentadiene ENDO & EXO V.2.svg Diene, Cycloalkene
C10H16
Phellandrene
Phellandrene alpha.svgPhellandrene beta.svg
Terpene, Diene Cycloalkene
C10H16
α-Terpinene Alpha-Terpinene Structure V.1.svg Terpene, Cycloalkene, Diene
C10H16
Limonene
(R)-Limonen.svg(S)-Limonen.svg
Terpene, Diene, Cycloalkene
C11H24
Undecane Undecan Skelett.svg Alkane
C30H50
Squalene Squalene.svg Terpene, Polyene
C2nH4n
Polyethylene Polyethylene repeat unit.svg Alkane


References




  1. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (1995) "aliphatic compounds".









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