Hydrocarbon

In organic chemistry, a hydrocarbon is an organic compound consisting entirely of hydrogen and carbon.[1]: 620 Hydrocarbons are examples of group 14 hydrides. Hydrocarbons are generally colourless and hydrophobic; their odor is usually faint, and may be similar to that of gasoline or lighter fluid. They occur in a diverse range of molecular structures and phases: they can be gases (such as methane and propane), liquids (such as hexane and benzene), low melting solids (such as paraffin wax and naphthalene) or polymers (such as polyethylene and polystyrene).

In the fossil fuel industries, hydrocarbon refers to naturally occurring petroleum, natural gas and coal, or their hydrocarbon derivatives and purified forms. Combustion of hydrocarbons is the main source of the world's energy. Petroleum is the dominant raw-material source for organic commodity chemicals such as solvents and polymers. Most anthropogenic (human-generated) emissions of greenhouse gases are either carbon dioxide released by the burning of fossil fuels, or methane released from the handling of natural gas or from agriculture.

## Contents

* 1 Types
* 2 Usage
* 3 Reactions
* 3.1 Saturated hydrocarbons
* 3.1.1 Cracking
* 3.2 Oxidation
* 3.2.1 Combustion
* 3.2.2 Halogenation
* 3.3 Unsaturated hydrocarbons
* 3.3.1 Substitution
* 3.3.2 Addition
* 3.4 Metathesis
* 4 Origin
* 5 Environmental impact
* 5.1 Bioremediation
* 6 Safety
* 7 See also
* 8 References

## Types

As defined by the International Union of Pure and Applied Chemistry's nomenclature of organic chemistry, hydrocarbons are classified as follows:[2]

1. Saturated hydrocarbons, which are the simplest of the hydrocarbon types. They are composed entirely of single bonds and are saturated with hydrogen. The formula for acyclic saturated hydrocarbons (i.e., alkanes) is CnH2n+2.[1]: 623 The most general form of saturated hydrocarbons, (whether linear or branched species, and whether with or without one or more rings) is CnH2n+2(1-r), where r is the number of rings. Those with exactly one ring are the cycloalkanes. Saturated hydrocarbons are the basis of petroleum fuels and may be either linear or branched species. One or more of the hydrogen atoms can be replaced with other atoms, for example chlorine or another halogen: this is called a substitution reaction. An example is the conversion of methane to chloroform using a chlorination reaction. Halogenating a hydrocarbon produces something that is not a hydrocarbon. It is a very common and useful process. Hydrocarbons with the same molecular formula but different structural formulae are called structural isomers.[1]: 625 As given in the example of 3-methylhexane and its higher homologues, branched hydrocarbons can be chiral.[1]: 627 Chiral saturated hydrocarbons constitute the side chains of biomolecules such as chlorophyll and tocopherol.[3]
2. Unsaturated hydrocarbons, which have one or more double or triple bonds between carbon atoms. Those with one or more double bonds are called alkenes. Those with one double bond have the formula CnH2n (assuming non-cyclic structures).[1]: 628 Those containing triple bonds are called alkyne. Those with one triple bond have the formula CnH2n−2.[1]: 631
3. Aromatic hydrocarbons, also known as arenes, which are hydrocarbons that have at least one aromatic ring. 10% of total nonmethane organic carbon emission are aromatic hydrocarbons from the exhaust of gasoline-powered vehicles.[citation needed]

The term 'aliphatic' refers to non-aromatic hydrocarbons. Saturated aliphatic hydrocarbons are sometimes referred to as 'paraffins'. Aliphatic hydrocarbons containing a double bond between carbon atoms are sometimes referred to as 'olefins'.

Variations on hydrocarbons based on the number of carbon atoms  Number of
carbon atoms  | Alkane (single bond)  | Alkene (double bond)  | Alkyne (triple bond)  | Cycloalkane | Alkadiene

|
|
|
|
|

1  | Methane | — | — | — | —
2  | Ethane | Ethene (ethylene) | Ethyne (acetylene) | — | —
3  | Propane | Propene (propylene) | Propyne (methylacetylene) | Cyclopropane | Propadiene (allene)
4  | Butane | Butene (butylene) | Butyne | Cyclobutane | Butadiene
5  | Pentane | Pentene | Pentyne | Cyclopentane | Pentadiene (piperylene)
6  | Hexane | Hexene | Hexyne | Cyclohexane | Hexadiene
7  | Heptane | Heptene | Heptyne | Cycloheptane | Heptadiene
8  | Octane | Octene | Octyne | Cyclooctane | Octadiene
9  | Nonane | Nonene | Nonyne | Cyclononane | Nonadiene
10  | Decane | Decene | Decyne | Cyclodecane | Decadiene
11  | Undecane | Undecene | Undecyne | Cycloundecane | Undecadiene
12  | Dodecane | Dodecene | Dodecyne | Cyclododecane | Dodecadiene

## Usage

Oil refineries are one way hydrocarbons are processed for use. Crude oil is processed in several stages to form desired hydrocarbons, used as fuel and in other products. Tank wagon 33 80 7920 362–0 with hydrocarbon gas at Bahnhof Enns (2018)

The predominant use of hydrocarbons is as a combustible fuel source. Methane is the predominant component of natural gas. C6 through C10 alkanes, alkenes, cycloalkanes, and aromatic hydrocarbons are the main components of gasoline, naphtha, jet fuel, and specialized industrial solvent mixtures. With the progressive addition of carbon units, the simple non-ring structured hydrocarbons have higher viscosities, lubricating indices, boiling points, and solidification temperatures. At the opposite extreme from methane lie the heavy tars that remain as the lowest fraction in a crude oil refining retort. They are collected and widely utilized as roofing compounds, pavement material (bitumen), wood preservatives (the creosote series) and as extremely high viscosity shear-resisting liquids.

Some large-scale non-fuel applications of hydrocarbons begin with ethane and propane, which are obtained from petroleum and natural gas. These two gases are converted either to syngas or to ethylene and propylene respectively. Global consumption of benzene in 2021 is estimated at more than 58 million metric tons, which will increase to 60 million tons in 2022.[4]

Hydrocarbons are also prevalent in nature. Some eusocial arthropods, such as the Brazilian stingless bee, Schwarziana quadripunctata, use unique cuticular hydrocarbon "scents" in order to determine kin from non-kin. This hydrocarbon composition varies between age, sex, nest location, and hierarchal position.[5]

There is also potential to harvest hydrocarbons from plants like Euphorbia lathyris and E. tirucalli as an alternative and renewable energy source for vehicles that use diesel.[6] Furthermore, endophytic bacteria from plants that naturally produce hydrocarbons have been used in hydrocarbon degradation in attempts to deplete hydrocarbon concentration in polluted soils.[7]

## Reactions

Saturated hydrocarbons are notable for their inertness. Unsaturated hydrocarbons (alkenes, alkynes and aromatic compounds) react more readily, by means of substitution, addition, polymerization. At higher temperatures they undergo dehydrogenation, oxidation and combustion.[2]

### Saturated hydrocarbons

#### Cracking

The cracking of saturated hydrocarbons is the main industrial route to alkenes and alkyne. These reactions require heterogeneous catalysts and temperatures >500 °C.

### Oxidation

Oxidation of hydrocarbons involves their reaction with oxygen. In the presence of excess oxygen, hydrocarbons combust. With careful conditions, which have been optimized for many years, partial oxidation results. Useful compounds can be obtained in this way: maleic acid from butane, terephthalic acid from xylenes, acetone together with phenol from cumene (isopropylbenzene), and cyclohexanone from cyclohexane. The process, which is called autoxidation, begins with the formation of hydroperoxides (ROOH).[8]

#### Combustion

Main article: Software:Combustion

Combustion of hydrocarbons is currently the main source of the world's energy for electric power generation, heating (such as home heating), and transportation.[9][10] Often this energy is used directly as heat such as in home heaters, which use either petroleum or natural gas. The hydrocarbon is burnt and the heat is used to heat water, which is then circulated. A similar principle is used to create electrical energy in power plants. Both saturated and unsaturated hydrocarbons undergo this process.

Common properties of hydrocarbons are the facts that they produce steam, carbon dioxide and heat during combustion and that oxygen is required for combustion to take place. The simplest hydrocarbon, methane, burns as follows:

CHA4methane+2OA2⟶COA2+2HA2O

In inadequate supply of air, carbon black and water vapour are formed:

CHA4methane+OA2⟶C+2HA2O

And finally, for any linear alkane of n carbon atoms,

CnH2n+2+(3n+12)OA2⟶nCOA2+(n+1)HA2O

Partial oxidation characterizes the reactions of alkenes and oxygen. This process is the basis of rancidification and paint drying.

Benzene burns with sooty flame when heated in air:

CA6HA6benzene+152OA2⟶6COA2+3HA2O

#### Halogenation

Main article: Chemistry:Free-radical halogenation

Saturated hydrocarbons react with chlorine and fluorine. In the case of chlorination, one of the chlorine atoms replaces a hydrogen atom. The reactions proceed via free-radical pathways, in which the halogen first dissociates into two neutral radical atoms (homolytic fission).

CH4 \+ Cl2 → CH3Cl + HCl
CH3Cl + Cl2 → CH2Cl2 \+ HCl

all the way to CCl4 (carbon tetrachloride)

C2H6 \+ Cl2 → C2H5Cl + HCl
C2H4Cl2 \+ Cl2 → C2H3Cl3 \+ HCl

all the way to C2Cl6 (hexachloroethane)

### Unsaturated hydrocarbons

#### Substitution

Main article: Chemistry:Substitution reaction

Aromatic compounds, almost uniquely for hydrocarbons, undergo substitution reactions. The chemical process practiced on the largest scale is the reaction of benzene and ethene to give ethylbenzene:

6 \+ C

4 → C

5CH
2CH

The resulting ethylbenzene is dehydrogenated to styrene and then polymerized to manufacture polystyrene, a common thermoplastic material.

#### Addition

Main articles: Chemistry:Addition reaction, Hydrogenation, and Polyolefin

Addition reactions apply to alkenes and alkynes. It is because they add reagents that they are called unsaturated. In this reaction a variety of reagents add "across" the pi-bond(s). Chlorine, hydrogen chloride, water, and hydrogen are illustrative reagents.

Polymerization is a form of addition. Alkenes and some alkynes undergo polymerization by opening of the multiple bonds to produce polyethylene, polybutylene, and polystyrene. The alkyne acetylene polymerizes to produce polyacetylene. Oligomers (chains of a few monomers) may be produced, for example in the Shell higher olefin process, where α-olefins are extended to make longer α-olefins by adding ethylene repeatedly.

### Metathesis

Some hydrocarbons undergo metathesis, in which substituents attached by C–C bonds are exchanged between molecules. For a single C–C bond it is alkane metathesis, for a double C–C bond it is alkene metathesis (olefin metathesis), and for a triple C–C bond it is alkyne metathesis.

## Origin

Natural oil spring in Korňa, Slovakia

The vast majority of hydrocarbons found on Earth occur in crude oil, petroleum, coal, and natural gas. For thousands of years they have been exploited and used for a vast range of purposes.[11] Petroleum (lit. rock oil) and coal are generally thought to be products of decomposition of organic matter. Coal, in contrast to petroleum, is richer in carbon and poorer in hydrogen. Natural gas is the product of methanogenesis.[12][13]

A seemingly limitless variety of compounds comprise petroleum, hence the necessity of refineries. These hydrocarbons consist of saturated hydrocarbons, aromatic hydrocarbons, or combinations of the two. Missing in petroleum are alkenes and alkynes. Their production requires refineries. Petroleum-derived hydrocarbons are mainly consumed for fuel, but they are also the source of virtually all synthetic organic compounds, including plastics and pharmaceuticals. Natural gas is consumed almost exclusively as fuel. Coal is used as a fuel and as a reducing agent in metallurgy.

A small fraction of hydrocarbon found on earth, and all currently known hydrocarbon found on other planets and moons, is thought to be abiological.[14]

Hydrocarbons such as ethylene, isoprene, and monoterpenes are emitted by living vegetation.[15]

Some hydrocarbons also are widespread and abundant in the Solar System. Lakes of liquid methane and ethane have been found on Titan, Saturn's largest moon, as confirmed by the Cassini–Huygens space probe.[16] Hydrocarbons are also abundant in nebulae forming polycyclic aromatic hydrocarbon compounds.[17]

## Environmental impact

Burning hydrocarbons as fuel, which produces carbon dioxide and water, is a major contributor to anthropogenic global warming. Hydrocarbons are introduced into the environment through their extensive use as fuels and chemicals as well as through leaks or accidental spills during exploration, production, refining, or transport of fossil fuels. Anthropogenic hydrocarbon contamination of soil is a serious global issue due to contaminant persistence and the negative impact on human health.[18]

Mechanisms involved in hydrocarbon phytoremediation[19]

When soil is contaminated by hydrocarbons, it can have a significant impact on its microbiological, chemical, and physical properties. This can serve to prevent, slow down or even accelerate the growth of vegetation depending on the exact changes that occur. Crude oil and natural gas are the two largest sources of hydrocarbon contamination of soil.[20]

### Bioremediation

Bioremediation of hydrocarbon from soil or water contaminated is a formidable challenge because of the chemical inertness that characterize hydrocarbons (hence they survived millions of years in the source rock). Nonetheless, many strategies have been devised, bioremediation being prominent. The basic problem with bioremediation is the paucity of enzymes that act on them. Nonetheless, the area has received regular attention.[21] Bacteria in the gabbroic layer of the ocean's crust can degrade hydrocarbons; but the extreme environment makes research difficult.[22] Other bacteria such as Lutibacterium anuloederans can also degrade hydrocarbons.[23] Mycoremediation or breaking down of hydrocarbon by mycelium and mushrooms is possible.[24][25]

## Safety

Main article: Medicine:Hydrocarbon poisoning

Hydrocarbons are generally of low toxicity, hence the widespread use of gasoline and related volatile products. Aromatic compounds such as benzene and toluene are narcotic and chronic toxins, and benzene in particular is known to be carcinogenic. Certain rare polycyclic aromatic compounds are carcinogenic. Hydrocarbons are highly flammable.

## See also

* Abiogenic petroleum origin
* Biomass to liquid
* Carbohydrate
* Energy storage
* Fractional distillation
* Functional group
* Hydrocarbon mixtures
* Organic nuclear reactor

## References

1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 Silberberg, Martin (2004). Chemistry: The Molecular Nature Of Matter and Change. New York: McGraw-Hill Companies. ISBN 0-07-310169-9.
2. ↑ 2.0 2.1 Schmidt, Roland; Griesbaum, Karl; Behr, Arno; Biedenkapp, Dieter; Voges, Heinz-Werner; Garbe, Dorothea; Paetz, Christian; Collin, Gerd et al. (2014). "Hydrocarbons". Ullmann's Encyclopedia of Industrial Chemistry. pp. 1–74. doi:10.1002/14356007.a13_227.pub3. ISBN 978-3-527-30673-2.
3. ↑ Meierhenrich, Uwe (2008). Amino Acids and the Asymmetry of Life: Caught in the Act of Formation. Berlin: Springer. ISBN 978-3-540-76886-9. OCLC 288470227. https://books.google.com/books?id=a2J23yPEaBQC.
4. ↑ "Benzene global market volume 2015-2026" (in en). https://www.statista.com/statistics/1245172/benzene-market-volume-worldwide/.
5. ↑ Nunes, T.M.; Turatti, I.C.C.; Mateus, S.; Nascimento, F.S.; Lopes, N.P.; Zucchi, R. (2009). "Cuticular Hydrocarbons in the Stingless Bee Schwarziana quadripunctata (Hymenoptera, Apidae, Meliponini): Differences between Colonies, Castes and Age". Genetics and Molecular Research 8 (2): 589–595. doi:10.4238/vol8-2kerr012. PMID 19551647. http://www.funpecrp.com.br/gmr/year2009/vol8-2/pdf/kerr012.pdf.
6. ↑ Calvin, Melvin (1980). "Hydrocarbons from plants: Analytical methods and observations". Naturwissenschaften 67 (11): 525–533. doi:10.1007/BF00450661. Bibcode: 1980NW.....67..525C. https://digital.library.unt.edu/ark:/67531/metadc827749/.
7. ↑ Pawlik, Malgorzata (2017). "Hydrocarbon degradation potential and plant growth-promoting activity of culturable endophytic bacteria of Lotus corniculatus and Oenothera biennis from a long-term polluted site". Environmental Science and Pollution Research International 24 (24): 19640–19652. doi:10.1007/s11356-017-9496-1. PMID 28681302. Bibcode: 2017ESPR...2419640P.
8. ↑ Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, p. 967, ISBN 978-0-471-72091-1, https://books.google.com/books?id=JDR-nZpojeEC&printsec=frontcover
9. ↑ "Generating Electricity" (in en-US). https://electricity.ca/learn/electricity-today/generating-electricity/.
10. ↑ Zou, Caineng; Zhao, Qun; Zhang, Guosheng; Xiong, Bo (2016-01-01). "Energy revolution: From a fossil energy era to a new energy era" (in en). Natural Gas Industry B 3 (1): 1–11. doi:10.1016/j.ngib.2016.02.001. ISSN 2352-8540. Bibcode: 2016NGIB....3....1Z.
11. ↑ van Dijk, J.P. (2022); Unravelling the Maze of Scientific Writing Through the Ages: On the Origins of the Terms Hydrocarbon, Petroleum, Natural Gas, and Methane. Amazon Publishers, 166 pp. PaperBack Edition B0BKRZRKHW. ISBN 979-8353989172
12. ↑ Clayden, J., Greeves, N., et al. (2001) Organic Chemistry Oxford ISBN 0-19-850346-6, p. 21.
13. ↑ McMurry, J. (2000). Organic Chemistry 5th ed. Brooks/Cole: Thomson Learning. ISBN 0-495-11837-0. pp. 75–81.
14. ↑ Sephton, M. A.; Hazen, R. M. (2013). "On the Origins of Deep Hydrocarbons". Reviews in Mineralogy and Geochemistry 75 (1): 449–465. doi:10.2138/rmg.2013.75.14. Bibcode: 2013RvMG...75..449S.
15. ↑ Dewulf, Jo. "Hydrocarbons in the Atmosphere". https://www.eolss.net/Sample-Chapters/C06/E6-13-02-07.pdf.
16. ↑ NASA's Cassini Spacecraft Reveals Clues About Saturn Moon. . NASA (12 December 2013).
17. ↑ Guzman-Ramirez, L.; Lagadec, E.; Jones, D.; Zijlstra, A. A.; Gesicki, K. (2014). "PAH formation in O-rich planetary nebulae". Monthly Notices of the Royal Astronomical Society 441 (1): 364–377. doi:10.1093/mnras/stu454. Bibcode: 2014MNRAS.441..364G.
18. ↑ Singh, S. N.; Kumari, B.; Mishra, Shweta (2012), Singh, Shree Nath, ed., "Microbial Degradation of Alkanes", Microbial Degradation of Xenobiotics (Berlin, Heidelberg: Springer Berlin Heidelberg): pp. 439–469, doi:10.1007/978-3-642-23789-8_17, ISBN 978-3-642-23788-1, https://www.researchgate.net/publication/226738847_Microbial_Degradation_of_Alkanes
19. ↑ Rohrbacher, Fanny; St-Arnaud, Marc (2016-03-09). "Root Exudation: The Ecological Driver of Hydrocarbon Rhizoremediation". Agronomy (MDPI AG) 6 (1): 19. doi:10.3390/agronomy6010019. ISSN 2073-4395. Bibcode: 2016Agron...6...19R.
20. ↑ "Additives Affecting the Microbial Degradation of Petroleum Hydrocarbons", Bioremediation of Contaminated Soils (CRC Press): pp. 353–360, 2000-06-09, doi:10.1201/9781482270235-27, ISBN 978-0-429-07804-0
21. ↑ Lim, Mee Wei; Lau, Ee Von; Poh, Phaik Eong (2016). "A comprehensive guide of remediation technologies for oil contaminated soil — Present works and future directions". Marine Pollution Bulletin 109 (1): 14–45. doi:10.1016/j.marpolbul.2016.04.023. PMID 27267117. Bibcode: 2016MarPB.109...14L.
22. ↑ "First investigation of the microbiology of the deepest layer of ocean crust.". PLOS ONE 5 (11). 2010. doi:10.1371/journal.pone.0015399. PMID 21079766. Bibcode: 2010PLoSO...515399M.
23. ↑ Yakimov, M. M.; Timmis, K. N.; Golyshin, P. N. (2007). "Obligate oil-degrading marine bacteria". Curr. Opin. Biotechnol. 18 (3): 257–266. doi:10.1016/j.copbio.2007.04.006. PMID 17493798.
24. ↑ Stamets, Paul (2008). "6 ways mushrooms can save the world" (video). https://www.ted.com/talks/paul_stamets_6_ways_mushrooms_can_save_the_world?language=en.
25. ↑ Stamets, Paul (2005). "Mycoremediation". Mycelium Running: How Mushrooms Can Help Save the World. Ten Speed Press. p. 86. ISBN 978-1-58008-579-3. https://archive.org/details/myceliumrunningh00stam_0/page/86.

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Organic chemistry affixes

Carbon-based|

* -ane (alkane)
* -ene (alkene)
* -ine (unsaturated hydrocarbon)
* -yne (alkyne)
* alk- (nonaromatic hydrocarbon)
* ar- (aromatic)
* cyclo- (cyclic)

Oxygen-based|

* -al (aldehyde)
* -oate (ester)
* -oic acid (carboxylic acid)
* -ol (alcohol)
* -one (ketone)
* -ose (sugar)

Nitrogen-based|

* -ine (alkaloid)
* aza- (N replaces C)

Sulfur-based|

* thio- (S replaces O)

Counting axial atoms|

* meth- (1)
* eth- (2)
* prop- (3)
* but- (4)
* (and the rest are ordinary Greek/Latin prefixes)

Other|

* -ase]] (enzyme)
* -yl (radical)

* v
* t
* e

Hydrocarbons

Saturated
aliphatic
hydrocarbons|

| Alkanes
CnH2n \+ 2|

| Linear alkanes|

* Methane
* Ethane
* Propane
* Butane
* Pentane
* Hexane
* Heptane
* Octane
* Nonane
* Decane

|

Branched alkanes|

* Isobutane
* Isopentane
* 3-Methylpentane
* Neopentane
* Isohexane
* Isoheptane
* Isooctane
* Isononane
* Isodecane

Cycloalkanes|

* Cyclopropane
* Cyclobutane
* Cyclopentane
* Cyclohexane
* Cycloheptane
* Cyclooctane
* Cyclononane
* Cyclodecane

Alkylcycloalkanes|

* Methylcyclopropane
* Methylcyclobutane
* Methylcyclopentane
* Methylcyclohexane
* Isopropylcyclohexane

Bicycloalkanes|

* Housane (bicyclo[2.1.0]pentane)
* Norbornane (bicyclo[2.2.1]heptane)
* Decalin (bicyclo[4.4.0]decane)

Polycycloalkanes|

* Adamantane
* Diamondoid
* Perhydrophenanthrene
* Sterane
* Cubane
* Prismane
* Dodecahedrane
* Basketane
* Churchane
* Pagodane
* Twistane

Other|

* Spiroalkanes

Unsaturated
aliphatic
hydrocarbons|

| Alkenes
CnH2n|

| Linear alkenes|

* Ethene
* Propene
* Butene
* Pentene
* Hexene
* Heptene
* Octene
* Nonene
* Decene

|

Branched alkenes|

* Isobutene
* Isopentene
* Isohexene
* Isoheptene
* Isooctene
* Isononene
* Isodecene

Alkynes
CnH2n − 2|

| Linear alkynes|

* Ethyne
* Propyne
* Butyne
* Pentyne
* Hexyne
* Heptyne
* Octyne
* Nonyne
* Decyne

|

Branched alkynes|

* Isopentyne
* Isohexyne
* Isoheptyne
* Isooctyne
* Isononyne
* Isodecyne

Cycloalkenes|

* Cyclopropene
* Cyclobutene
* Cyclopentene
* Cyclohexene
* Cycloheptene
* Cyclooctene
* Cyclononene
* Cyclodecene

Alkylcycloalkenes|

* Methylcyclopropene
* Methylcyclobutene
* Methylcyclopentene
* Methylcyclohexene
* Isopropylcyclohexene

Bicycloalkenes|

* Norbornene

Cycloalkynes|

* Cyclopropyne
* Cyclobutyne
* Cyclopentyne
* Cyclohexyne
* Cycloheptyne
* Cycloctyne
* Cyclononyne
* Cyclodecyne

Dienes|

* Propadiene
* Butadiene
* Pentadiene
* Hexadiene
* Heptadiene
* Octadiene
* Nonadiene
* Decadiene

Other|

* Alkatriene
* Alkadiyne
* Cumulene
* Cyclooctatetraene
* Cyclododecatriene
* Enyne

Aromatic
hydrocarbons|

| PAHs|

| Acenes|

* Naphthalene
* Anthracene
* Tetracene
* Pentacene
* Hexacene
* Heptacene

|

Other|

* Azulene
* Fluorene
* Helicenes
* Circulenes
* Butalene
* Phenanthrene
* Chrysene
* Pyrene
* Corannulene
* Kekulene

Alkylbenzenes|

* Toluene
* Xylene
* Ethylbenzene
* Cumene
* Styrene
* Mesitylene
* Pseudocumene
* Hemellitene
* Cymene
* Hexamethylbenzene

Other|

* Benzene
* Cyclopropenylidene

Other|

* Annulenes
* Annulynes
* Alicyclic compounds
* Petroleum jelly

* v
* t
* e

Transport of hydrocarbon fuels

Oil|

* Oil tanker
* Oil terminal
* Tank car
* Tank truck
* List of oil pipelines

LNG and LPG|

* LNG carrier
* Regasification
* Liquefaction
* Gas separation
* Natural gas storage
* Black powder in gas pipelines
* List of natural gas pipelines
* List of LNG terminals

Coal/Misc.|

* Industrial railway
* Intermodal freight transport
* Syngas

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