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In organic chemistry, xylene or xylol (from Greek ξύλον (xylon) 'wood'; [1] [2] IUPAC name: dimethylbenzene) are any of three organic compounds with the formula (CH 3) 2 C 6 H 4. They are derived from the substitution of two hydrogen atoms with methyl groups in a benzene ring; which hydrogens are substituted determines which of three ...
o-Xylene (ortho-xylene) is an aromatic hydrocarbon with the formula C 6 H 4 (CH 3) 2, with two methyl substituents bonded to adjacent carbon atoms of a benzene ring (the ortho configuration). It is a constitutional isomer of m-xylene and p-xylene, the mixture being called xylene or xylenes. o-Xylene is a colourless slightly oily flammable ...
p-Xylene (para-xylene) is an aromatic hydrocarbon. It is one of the three isomers of dimethylbenzene known collectively as xylenes . The p- stands for para- , indicating that the two methyl groups in p -xylene occupy the diametrically opposite substituent positions 1 and 4.
To avoid long and tedious names in normal communication, the official IUPAC naming recommendations are not always followed in practice, except when it is necessary to give an unambiguous and absolute definition to a compound. IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively simple ...
The main structure of chemical names according to IUPAC nomenclature. IUPAC nomenclature is a set of recommendations for naming chemical compounds and for describing chemistry and biochemistry in general. The International Union of Pure and Applied Chemistry (IUPAC) is the international authority on chemical nomenclature and terminology.
m-Xylene (meta-xylene) is an aromatic hydrocarbon. It is one of the three isomers of dimethylbenzene known collectively as xylenes . The m- stands for meta- , indicating that the two methyl groups in m -xylene occupy positions 1 and 3 on a benzene ring.
for o-Xylene/Carbon tetrachloride [8] P = 760 mm Hg BP Temp. °C % by mole carbon tetrachloride liquid vapor 142.0: 1.8: 6.5 136.0: 6.4: 22.9 130.4: 11.2: 36.9 125.0 ...
For example, reaction of α,α'-dibromo-o-xylene with iron carbonyls affords low yields of the xylylene complex Fe(CO) 3 [η 4-C 6 H 4 (CH 2) 2]. This product is structurally analogous to Fe(CO) 3 [η 4-1,3-butadiene]. [11] At high temperatures, benzocyclobutenes undergo electrocyclic ring-opening to form o-xylylenes.