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  2. Anisole - Wikipedia

    en.wikipedia.org/wiki/Anisole

    Anisole undergoes electrophilic aromatic substitution reaction at a faster speed than benzene, which in turn reacts more quickly than nitrobenzene.The methoxy group is an ortho/para directing group, which means that electrophilic substitution preferentially occurs at these three sites.

  3. Methoxy group - Wikipedia

    en.wikipedia.org/wiki/Methoxy_group

    In organic chemistry, a methoxy group is the functional group consisting of a methyl group bound to oxygen. This alkoxy group has the formula R−O−CH 3 . On a benzene ring , the Hammett equation classifies a methoxy substituent at the para position as an electron-donating group , but as an electron-withdrawing group if at the meta position.

  4. IUPAC nomenclature of organic chemistry - Wikipedia

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

    Common names for ketones can be derived by naming the two alkyl or aryl groups bonded to the carbonyl group as separate words followed by the word ketone. Acetone; Acetophenone; Benzophenone; Ethyl isopropyl ketone; Diethyl ketone; The first three of the names shown above are still considered to be acceptable IUPAC names.

  5. Phenol ether - Wikipedia

    en.wikipedia.org/wiki/Phenol_ether

    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 ...

  6. Dihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzenes

    Trivial name Catechol: Resorcinol: Hydroquinone: IUPAC name benzene-1,2-diol benzene-1,3-diol benzene-1,4-diol Other names pyrocatechol 1,2-dihydroxybenzene o-dihydroxybenzene o-benzenediol resorcin 1,3-dihydroxybenzene m-dihydroxybenzene m-benzenediol 1,4-dihydroxybenzene p-dihydroxybenzene p-benzenediol Structure

  7. 1,4-Dimethoxybenzene - Wikipedia

    en.wikipedia.org/wiki/1,4-Dimethoxybenzene

    It occurs naturally in willow (), tea, hyacinth, zucchini (Cucurbita pepo). [3] It appears to attract bees as it has a powerful response in their antenna. [4] In a study in mice, Iranian scientists identified 1,4-dimethoxybenzene as the major psychoactive chemical in musk willow (Salix aegyptiaca) by its ability to cause somnolescence and depressed activity.

  8. Cancer-causing chemical found in Clinique, Clearasil acne ...

    www.aol.com/news/cancer-causing-chemical-found...

    Benzene was also detected in Proactiv, PanOxyl, Walgreens' acne soap bar and Walmart's Equate Beauty acne cream among others, according to Valisure. Cancer-causing chemical found in Clinique ...

  9. Methoxytoluene - Wikipedia

    en.wikipedia.org/wiki/Methoxytoluene

    They consist of a disubstituted benzene ring with methoxy group and one methyl group. All three are colorless flammable liquids which are soluble in organic solvents but poorly soluble in water. They are not of major commercial interest although they are precursors to the corresponding methoxybenzoic acids and methoxybenzaldehydes. [1]