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  2. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    Ethers (R−O−R) consist of an oxygen atom between the two attached carbon chains. The shorter of the two chains becomes the first part of the name with the -ane suffix changed to -oxy, and the longer alkane chain becomes the suffix of the name of the ether. Thus, CH 3 OCH 3 is methoxymethane, and CH 3 OCH 2 CH 3 is methoxyethane (not ...

  3. Benzyl group - Wikipedia

    en.wikipedia.org/wiki/Benzyl_group

    In IUPAC nomenclature, the prefix benzyl refers to a C 6 H 5 CH 2 substituent, for example benzyl chloride or benzyl benzoate. Benzyl is not to be confused with phenyl with the formula C 6 H 5 . The term benzylic is used to describe the position of the first carbon bonded to a benzene or other aromatic ring.

  4. Ethyl phenyl ether - Wikipedia

    en.wikipedia.org/wiki/Ethyl_phenyl_ether

    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 ...

  5. Benzyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Benzyl_alcohol

    Benzyl alcohol is used effectively for treating lice infestations as the active ingredient in lotion shampoo with 5% benzyl alcohol. [ 12 ] Benzyl alcohol is an ingredient used in the manufacture of soaps, topical creams, skin lotions, shampoos, and facial cleansers and is popular due to its anti-bacterial and anti-fungal properties.

  6. Allyl phenyl ether - Wikipedia

    en.wikipedia.org/wiki/Allyl_phenyl_ether

    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.

  7. Phenol ether - Wikipedia

    en.wikipedia.org/wiki/Phenol_ether

    Examples of phenol ethers and their nomenclature. 5-phenoxynonane follows the same naming scheme as 1-phenoxyoctane, due to nonane having more carbons than a benzene ring. When substituents on aromatic rings are present, standard IUPAC nomenclature should be followed when naming aromatic compounds.

  8. Anisole - Wikipedia

    en.wikipedia.org/wiki/Anisole

    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.

  9. Phenethyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Phenethyl_alcohol

    Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C 6 H 5 CH 2 CH 2 OH.It is a colourless liquid with a pleasant floral odor. It occurs widely in nature, being found in a variety of essential oils.