Search results
Results from the WOW.Com Content Network
Structurally, it is an ether (−O−) with a methyl (−CH 3) and phenyl (−C 6 H 5) group attached. Anisole is a standard reagent of both practical and pedagogical value. Anisole is a standard reagent of both practical and pedagogical value.
ChemAxon Name <> Structure – ChemAxon IUPAC (& traditional) name to structure and structure to IUPAC name software. As used at chemicalize.org; chemicalize.org A free web site/service that extracts IUPAC names from web pages and annotates a 'chemicalized' version with structure images. Structures from annotated pages can also be searched.
IUPAC rules are often not followed for simple ethers. The trivial names for simple ethers (i.e., those with none or few other functional groups) are a composite of the two substituents followed by "ether". For example, ethyl methyl ether (CH 3 OC 2 H 5), diphenylether (C 6 H 5 OC 6 H 5). As for other organic compounds, very common ethers ...
Some sulfides are named by modifying the common name for the corresponding ether. For example, C 6 H 5 SCH 3 is methyl phenyl sulfide, but is more commonly called thioanisole, since its structure is related to that for anisole, C 6 H 5 OCH 3. The modern systematic nomenclature in chemistry for the trival name thioether is sulfane. [2]
Anisole is formally known as methoxybenzene, and is formed through the condensation of methanol (CH 3 OH) and phenol; due to the methyl group attached to the ethereal oxygen being smaller than the aromatic benzene ring, the benzene takes priority when naming the molecule. However, 1-phenoxyoctane has an octane substituent, which has a greater ...
Ethyl phenyl ether (or phenetole) is an organic compound that belongs to a class of compounds called ethers. Ethyl phenyl ether has the same properties as some other ethers, such as volatility, explosive vapors, and the ability to form peroxides. It will dissolve in less polar solvents such as ethanol or ether, but not in polar solvents such as ...
Benzyl group and derivatives: Benzyl group, benzyl radical, benzyl amine, benzyl bromide, benzyl chloroformate, and benzyl methyl ether. R = heteroatom, alkyl, aryl, allyl etc. or other substituents. In organic chemistry, benzyl is the substituent or molecular fragment possessing the structure R−CH 2 −C 6 H 5.
Allyl phenyl ether is prepared by the reaction of sodium phenoxide with allyl bromide: [1]. C 6 H 5 ONa + BrCH 2 CH=CH 2 → C 6 H 5 OCH 2 CH=CH 2 + NaBr. The yield is almost quantitative when the reaction is conducted in homogeneous solution using dimethoxyethane.