An organic compound consisting exclusively of the elements carbon and hydrogen. Derived principally from petroleum, coal tar, and plant sources. Following is a resume of the principal types.
Aliphatic (straight-chain)
Paraffins (alkanes): generic formula CnH2n+2. Saturated, single bonds only.
Acetylenes: generic formula CnH2n-2. Unsaturated (triple bond).
Acyclic terpenes. Unsaturated (polymers of isoprene, C5H8).Note: Some aliphatic compounds have branched chains in which the subchain also contains carbon atoms (isobutane); both chains are essentially straight.
Cyclic (closed ring)
Alicyclic: three or more carbon atoms in a ring structure with properties similar to those of aliphatics.
Cycloparaffins (naphthenes): saturated compounds often having a boat or chair structure, e.g., cyclohexane, cyclopentane.
Cycloolefins: unsaturated, two or more double bonds, e.g., cyclopentadiene (2), cyclooctatetraene (4).
Aromatic: unsaturated, hexagonal ring structure (three double bonds), single rings and double or triple fused rings.
benzene group (1 ring).
naphthalene group (2 rings).
anthracene group (3 rings).
Cyclic terpenes: monocyclic (dipentene); dicyclic (pinene).Note: Olefinic (isoprenoid) hydrocarbons are produced by a number of plants, notably Hevea braziliensis (rubber), guayule, and various members of the Euphorbiaceae family. Current research on the latter group indicates that they could be used as a source of liquid fuels and chemical feedstocks by genetic modification of the plants and control of their molecular constitution. It is estimated that oil obtained by large-scale cultivation of such plants, which grow well in semi-arid environments, could become economically competitive with petroleum within a few years.