User:Luckytooth/Alkylbenzene

Original article
The alkylbenzenes are derivatives of benzene, in which one or more hydrogen atoms are replaced by alkyl groups of different sizes. They are a subset of the aromatic hydrocarbons. The simplest member is toluene, in which a hydrogen atom of the benzene was replaced by a methyl group.

Literature

 * Allinger, Cava, de Jongh, Johnson, Lebel, Stevens: Organische Chemie, 1. Auflage, Walter de Gruyter, Berlin 1980, ISBN 3-11-004594-X, pp. 367–368, 560–562.
 * Streitwieser / Heathcock: Organische Chemie, 1. Auflage, Verlag Chemie, Weinheim 1980, ISBN 3-527-25810-8, pp. 1051, 1073–1080.
 * Beyer / Walter: Lehrbuch der Organischen Chemie, 19. Auflage, S. Hirzel Verlag, Stuttgart 1981, ISBN 3-7776-0356-2, pp. 442–444.
 * Morrison / Boyd: Lehrbuch der Organischen Chemie, 3. Auflage, Verlag Chemie, Weinheim 1986, ISBN 3-527-26067-6, pp. 707–728.

Improved Article
Alkylbenzenes are monocyclic aromatic compounds with saturated side chains. They are derivatives of benzene, in which one or more hydrogen atoms are replaced by alkyl groups. The simplest member is toluene, in which a hydrogen atom of the benzene was replaced by a methyl group. The chemical formula of alkylbenzenes is CnH2n-6. Alkylbenzene is a very important class of hydrocarbons, especially in the synthetic production industry. Alkylbenzenes are the raw material in the production of synthetic sulfonate detergents, which are found in a variety of household products such as soap, shampoo, toothpaste, laundry detergent, etc. Linear alkylbenzenes (LAB) and branched alkylbenzenes (BAB) are families of alkylbenzene used to prepare synthetic sulfonates, however, LABs are more industrially favoured since the discovery of its extensive biodegradable yield over BAB-based sulfonates in the 1960s.

Reactions

 * Friedel-Crafts alkylation: alkylbenzene can be synthesized from olefins or alkyl halides with aromatic compounds in the presence of a catalyst such as AlCl3, HF, or H2SO4.


 * Gattermann-Koch reaction: named after German chemists Ludwig Gattermann and Julius Arnold Koch, the Gattermann-Koch reaction is a catalyzed formylation of alkylbenzenes with carbon monoxide and hydrochloric acid.
 * Alkylbenzene sulfonation reaction: electrophilic addition of a sulfonic acid group onto the aromatic ring.

Spectroscopy
Alkylbenzene isomers can be differentiated by observing the position of alkyl substituents on the benzene ring using Chemical ionization-proton exchange mass spectrometry. Conventional GC-MS yields limited results because the isomers have identical molecular weight and substituents.

Production
Some alkylbenzenes such as toluene, trimethylbenzenes, and tetramethylbenzenes occur naturally in coal tar oil and as byproducts of the crude oil refinery process. Others can be prepared by Friedel – Crafts alkylation.

Alkylbenzenes used to be synthesized from tetrapropylene, however, the reaction is now rarely used because of the low biodegradable alkylbenzene sulfonates it yields.

Safety hazards
Alkylbenzenes are flammable. Most of them are eye and skin irritants and pose an acute health hazard when ingested. Alkylbenzenes are toxic to aquatic life with long-lasting effects.

Synthetic sulfonates
Alkylbenzenes are the primary raw material in making synthetic alkylbenzene sulfonates. Synthetic sulfonates are the most widely used detergents, as industrial oil, emulsifiers, demulsifiers, rust inhibitors, dispersants, surfactants for enhanced oil recovery, ore-floatation agents, and wetting agents, among others. LAB such as alkylbenzene, dialkylbenzene, and alkyltoluene are most commonly used to prepare sulfonate detergents.

Solvent use
Some less substituented alkylbenzenes such as toluene and xylene are commonly used as solvents industrially.