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The compound in which a benzene ring is fused to arsole — typically on the carbon atoms 3 and 4 — is known as benzarsole. [3] Cumene (C 9 H 12), an aromatic hydrocarbon used in the production of phenol and acetone. Cummingtonite ((Mg,Fe 2+) 2 (Mg,Fe 2+) 5 Si 8 O 22 (OH) 2), a magnesium-iron silicate hydroxide, first identified in Cummington ...
Heteroarenes are aromatic compounds, where at least one methine or vinylene (-C= or -CH=CH-) group is replaced by a heteroatom: oxygen, nitrogen, or sulfur. [3] 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 ...
[1] [2] Simple aromatic rings can be heterocyclic if they contain non-carbon ring atoms, for example, oxygen, nitrogen, or sulfur. They can be monocyclic as in benzene, bicyclic as in naphthalene, or polycyclic as in anthracene. Simple monocyclic aromatic rings are usually five-membered rings like pyrrole or six-membered rings like pyridine.
The term benzylic is used to describe the position of the first carbon bonded to a benzene or other aromatic ring. For example, (C 6 H 5)(CH 3) 2 C + is referred to as a "benzylic" carbocation. The benzyl free radical has the formula C 6 H 5 CH 2 •.
The C 2 benzenes are a class of organic aromatic compounds which contain a benzene ring and two other carbon atoms. For the hydrocarbons with no further unsaturation, there are four isomers. There are three xylenes and one ethylbenzene .
The Buchner ring expansion reaction was first used in 1885 by Eduard Buchner and Theodor Curtius [1] [2] who prepared a carbene from ethyl diazoacetate for addition to benzene using both thermal and photochemical pathways in the synthesis of cycloheptatriene derivatives. The resulting product was a mixture of four isomeric carboxylic acids ...
This benzene ring is attached to carbon 3 and 4 of the fluorene-derived molecule. The 3D structure of benzo[c]fluorene is depicted in the infobox on the right as well. It is mostly flat, because it consists of 3 aromatic rings. Only the 2 hydrogen atoms on the 5 ring are oriented into the 3D plane.
This group typically excludes compounds in which either benzene is fused to another ring (bicyclic, tricyclic, polycyclic) [1] or includes a heteroatom, or where the methane connects to three or four benzenes. Ball-and-stick model of the benzhydryl radical. The benzhydryl radical can be abbreviated Ph 2 CH• or Bzh. [2]