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  2. Methoxy group - Wikipedia

    en.wikipedia.org/wiki/Methoxy_group

    The structure of a typical 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.

  3. CH3O - Wikipedia

    en.wikipedia.org/wiki/CH3O

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  4. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    Different ways of representing a methyl group (highlighted in blue). In organic chemistry, a methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms, having chemical formula CH 3 (whereas normal methane has the formula CH 4).

  5. Alkoxide - Wikipedia

    en.wikipedia.org/wiki/Alkoxide

    Alkali metal alkoxides are often oligomeric or polymeric compounds, especially when the R group is small (Me, Et). [3] [page needed] The alkoxide anion is a good bridging ligand, thus many alkoxides feature M 2 O or M 3 O linkages.

  6. Auxochrome - Wikipedia

    en.wikipedia.org/wiki/Auxochrome

    Hence the molecule appears coloured. When auxochromes are attached to the molecule, the natural frequency of the chromophore gets changed and thus the colour gets modified. Different auxochromes produce different effects in the chromophore which in turn causes absorption of light from other parts of the spectrum.

  7. Potassium methoxide - Wikipedia

    en.wikipedia.org/wiki/Potassium_methoxide

    Potassium methoxide is a white to yellowish, hygroscopic, odorless crystalline powder which reacts violently with water forming potassium hydroxide and methanol. The aqueous solutions obtained are highly basic and have a corrosive effect. The substance is classified as an inflammable solid with a spontaneous ignition temperature of 70 °C. [6]

  8. Sodium methoxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_methoxide

    Sodium methoxide is prepared by treating methanol with sodium: 2 Na + 2 CH 3 OH → 2 CH 3 ONa + H 2. The reaction is so exothermic that ignition is possible. The resulting solution, which is colorless, is often used as a source of sodium methoxide, but the pure material can be isolated by evaporation followed by heating to remove residual methanol.

  9. Methanol - Wikipedia

    en.wikipedia.org/wiki/Methanol

    Methanol and its vapours are flammable. Moderately toxic for small animals – Highly toxic to large animals and humans (in high concentrations) – May be fatal/lethal or cause blindness and damage to the liver, kidneys, and heart if swallowed – Toxicity effects from repeated over exposure have an accumulative effect on the central nervous system, especially the optic nerve – Symptoms may ...