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  2. Methanol - Wikipedia

    en.wikipedia.org/wiki/Methanol

    Methanol (also called methyl alcohol and wood spirit, amongst other names) is an organic chemical compound and the simplest aliphatic alcohol, with the chemical formula C H 3 OH (a methyl group linked to a hydroxyl group, often abbreviated as MeOH).

  3. Benzyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Benzyl_alcohol

    Benzyl alcohol (also known as α-cresol) is an aromatic alcohol with the formula C 6 H 5 CH 2 OH. The benzyl group is often abbreviated "Bn" (not to be confused with "Bz" which is used for benzoyl), thus benzyl alcohol is denoted as BnOH.

  4. Cresol - Wikipedia

    en.wikipedia.org/wiki/Cresol

    Dipole moment: 1.35 D: 1.61 D: 1.58 D: Hazards SDS: Main hazards: flammable, ingestion and inhalation toxicity hazard Flash point: 81 °C c.c. 86 °C 86 °C c.c. GHS pictograms: RTECS number GO6300000 GO6125000 GO6475000 Related compounds Related phenols: xylenols: Related compounds bromocresol green, cresol red: Except where noted otherwise ...

  5. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    Note that the dipole moments drawn in this diagram represent the shift of the valence electrons as the origin of the charge, which is opposite the direction of the actual electric dipole moment. The bond dipole moment [5] uses the idea of electric dipole moment to measure the polarity of a chemical bond within a molecule. It occurs whenever ...

  6. Dipolar compound - Wikipedia

    en.wikipedia.org/wiki/Dipolar_compound

    In most dipolar compounds the charges are delocalized. [1] Unlike salts, dipolar compounds have charges on separate atoms, not on positive and negative ions that make up the compound. Dipolar compounds exhibit a dipole moment. Dipolar compounds can be represented by a resonance structure.

  7. Dimethyl ether - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_ether

    The simplest ether, it is a colorless gas that is a useful precursor to other organic compounds and an aerosol propellant that is currently being demonstrated for use in a variety of fuel applications. Dimethyl ether was first synthesised by Jean-Baptiste Dumas and Eugene Péligot in 1835 by distillation of methanol and sulfuric acid. [5]

  8. Formaldehyde - Wikipedia

    en.wikipedia.org/wiki/Formaldehyde

    Formaldehyde (/ f ɔːr ˈ m æ l d ɪ h aɪ d / ⓘ for-MAL-di-hide, US also / f ə r-/ ⓘ fər-) (systematic name methanal) is an organic compound with the chemical formula CH 2 O and structure H−CHO, more precisely H 2 C=O. The compound is a pungent, colourless gas that polymerises spontaneously into paraformaldehyde.

  9. Dimethoxymethane - Wikipedia

    en.wikipedia.org/wiki/Dimethoxymethane

    It can be manufactured by oxidation of methanol or by the reaction of formaldehyde with methanol. In aqueous acid, it is hydrolyzed back to formaldehyde and methanol.. Due to the anomeric effect, dimethoxymethane has a preference toward the gauche conformation with respect to each of the C–O bonds, instead of the anti conformation.