Hydrocarbon compounds without aromatic rings
Acyclic aliphatic/non-aromatic compound (butane ) Cyclic aliphatic/non-aromatic compound (cyclobutane )
In organic chemistry , hydrocarbons (compounds composed solely of carbon and hydrogen ) are divided into two classes: aromatic compounds and aliphatic compounds (; G. aleiphar , fat, oil). Aliphatic compounds can be saturated (in which all the C-C bonds are single requiring the structure to be completed, or 'saturated', by hydrogen) like hexane , or unsaturated , like hexene and hexyne . Open-chain compounds , whether straight or branched, and which contain no rings of any type, are always aliphatic. Cyclic compounds can be aliphatic if they are not aromatic .[ 1]
Structure
Aliphatic compounds can be saturated , joined by single bonds (alkanes ), or unsaturated, with double bonds (alkenes ) or triple bonds (alkynes ). If other elements (heteroatoms ) are bound to the carbon chain , the most common being oxygen , nitrogen , sulfur , and chlorine , it is no longer a hydrocarbon, and therefore no longer an aliphatic compound. However, such compounds may still be referred to as aliphatic if the hydrocarbon portion of the molecule is aliphatic, e.g. aliphatic amines , to differentiate them from aromatic amines .
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 natural gas for stoves or heating; butane in torches and lighters ; various aliphatic (as well as aromatic) hydrocarbons in liquid transportation fuels like petrol/gasoline , diesel , and jet fuel ; and other uses such as ethyne (acetylene) in welding .
Examples of aliphatic compounds
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
Alkane
C2 H2
Acetylene
Alkyne
C2 H4
Ethylene
Alkene
C2 H6
Ethane
Alkane
C3 H4
Propyne
Alkyne
C3 H6
Propene
Alkene
C3 H8
Propane
Alkane
C4 H6
1,2-Butadiene
Diene
C4 H6
1-Butyne
Alkyne
C4 H8
1-Butene
Alkene
C4 H10
Butane
Alkane
C6 H10
Cyclohexene
Cycloalkene
C5 H12
n -pentane
Alkane
C7 H14
Cycloheptane
Cycloalkane
C7 H14
Methylcyclohexane
Cyclohexane
C8 H8
Cubane
Prismane , Platonic hydrocarbon
C9 H20
Nonane
Alkane
C10 H12
Dicyclopentadiene
Diene, Cycloalkene
C10 H16
Phellandrene
Terpene , Diene, Cycloalkene
C10 H16
α-Terpinene
Terpene, Diene, Cycloalkene
C10 H16
Limonene
Terpene, Diene, Cycloalkene
C11 H24
Undecane
Alkane
C30 H50
Squalene
Terpene, Polyene
C2n H4n
Polyethylene
Alkane
References