1,3-Diisopropylbenzene

	1,3-Diisopropylbenzene 1,3-Diisopropylbenzene is an aromatic hydrocarbon with the formula C6H4(CHMe2)2 (Me = CH3). It is one of three isomeric diisopropylbenzenes. This colorless liquid is prepared by thermal isomerization of 1,4-diisopropylbenzene over a solid acid catalyst. It is the principal industrial precursor to resorcinol via the Hock rearrangement Hock may refer to: Common meanings: * Hock (wine), a type of wine * Hock (anatomy), part of an animal's leg * To leave an item with a pawnbroker People: * Hock (surname) * Richard "Hock" Walsh (1948-1999), Canadian blues singer Other uses: * A .... References {{DEFAULTSORT:Diisopropylbenzene, 1,3- Alkylbenzenes Isopropyl compounds ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu]
picture info	Diisopropylbenzenes In organic chemistry, the diisopropylbenzenes constitute a group of aromatic hydrocarbons, whose chemical structure consists of a benzene ring () with two isopropyl groups () as substituents. Through their different arrangement, they form three structural isomers with the molecular formula . References {{Commonscat Alkylbenzenes Isopropyl compounds ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu]
picture info	Resorcinol Resorcinol (or resorcin) is an organic compound with the formula C6H4(OH)2. It is one of three isomeric benzenediols, the 1,3-isomer (or '' meta''-isomer). Resorcinol crystallizes from benzene as colorless needles that are readily soluble in water, alcohol, and ether, but insoluble in chloroform and carbon disulfide. Production Resorcinol is produced in several steps from benzene, starting with dialkylation with propylene to give 1,3-diisopropylbenzene. Oxidation and Hock rearrangement of this disubstituted arene gives acetone and resorcinol. Resorcinol is an expensive chemical, produced in only a very few locations around the world (to date only four commercial plants are known to be operative: in the United States, Germany,China and Japan), and as such it is the determining factor in the cost of PRF adhesives. Many additional routes exist for resorcinol. It was formerly produced by disulfonation of benzene followed by hydrolysis of the 1,3-disulfonate. This method ha ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu]
picture info	Aromatic Hydrocarbon Aromatic compounds, also known as "mono- and polycyclic aromatic hydrocarbons", are organic compounds containing one or more aromatic rings. The parent member of aromatic compounds is benzene. The word "aromatic" originates from the past grouping of molecules based on smell, before their general chemical properties are understood. The current definition of aromatic compounds does not have any relation with their smell. Heteroarenes are closely related, since at least one carbon atom of CH group is replaced by one of the heteroatoms oxygen, nitrogen, or sulfur. Examples of non-benzene compounds with aromatic properties are furan, a heterocyclic compound with a five-membered ring that includes a single oxygen atom, and pyridine, a heterocyclic compound with a six-membered ring containing one nitrogen atom. Hydrocarbons without an aromatic ring are called aliphatic. Benzene ring model Benzene, C6H6, is the least complex aromatic hydrocarbon, and it was the first one named as such ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu]
picture info	Solid Acid Solid is one of the four fundamental states of matter (the others being liquid, gas, and plasma). The molecules in a solid are closely packed together and contain the least amount of kinetic energy. A solid is characterized by structural rigidity and resistance to a force applied to the surface. Unlike a liquid, a solid object does not flow to take on the shape of its container, nor does it expand to fill the entire available volume like a gas. The atoms in a solid are bound to each other, either in a regular geometric lattice (crystalline solids, which include metals and ordinary ice), or irregularly (an amorphous solid such as common window glass). Solids cannot be compressed with little pressure whereas gases can be compressed with little pressure because the molecules in a gas are loosely packed. The branch of physics that deals with solids is called solid-state physics, and is the main branch of condensed matter physics (which also includes liquids). Materials science ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu]
	Hock Rearrangement Hock may refer to: Common meanings: * Hock (wine), a type of wine * Hock (anatomy), part of an animal's leg * To leave an item with a pawnbroker People: * Hock (surname) * Richard "Hock" Walsh (1948-1999), Canadian blues singer Other uses: * A type of wine bottle used primarily for German or Alsatian wine See also * Hock Mountain, a summit in Washington state * Hocktide Hocktide, Hock tide or Hoke Day is a very old term used to denote the Monday and Tuesday in the second week after Easter. It was an English medieval festival; both the Tuesday and the preceding Monday were the Hock-days. Together with Whitsuntid ... or Hock tide, an English holiday consisting of Hock Monday and Hock Tuesday {{disambig ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu]
picture info	Alkylbenzenes 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 In organic chemistry, a methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms, having chemical formula . In formulas, the group is often abbreviated as Me. This hydrocarbon group occurs in many .... Literature * Allinger, Cava, de Jongh, Johnson, Lebel, Stevens: ''Organische Chemie'', 1. Auflage, Walter de Gruyter, Berlin 1980, , pp. 367–368, 560–562. * Streitwieser / Heathcock: ''Organische Chemie'', 1. Auflage, Verlag Chemie, Weinheim 1980, , pp. 1051, 1073–1080. * Beyer / Walter: ''Lehrbuch der Organischen Chemie'', 19. Auflage, S. Hirzel Verlag, Stuttgart 1981, , pp. 442–444. * Morrison / Boyd: ''Lehrbuch der Organischen ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu]