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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. 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.

  4. Acetyl group - Wikipedia

    en.wikipedia.org/wiki/Acetyl_group

    In organic chemistry, an acetyl group is a functional group denoted by the chemical formula −COCH 3 and the structure −C(=O)−CH 3.It is sometimes represented by the symbol Ac [5] [6] (not to be confused with the element actinium).

  5. Dimethyl ether - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_ether

    It is also used in refrigerant blends with e.g. ammonia, carbon dioxide, butane and propene. Dimethyl ether was the first refrigerant. Dimethyl ether was the first refrigerant. In 1876, the French engineer Charles Tellier bought the ex-Elder-Dempster a 690 tons cargo ship Eboe and fitted a methyl-ether refrigerating plant of his design.

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  7. 2,2-Dimethoxypropane - Wikipedia

    en.wikipedia.org/wiki/2,2-Dimethoxypropane

    2,2-Dimethoxypropane (DMP) is an organic compound with the formula (CH 3) 2 C(OCH 3) 2.A colorless liquid, it is the product of the condensation of acetone and methanol.DMP is used as a water scavenger in water-sensitive reactions.

  8. Functional group - Wikipedia

    en.wikipedia.org/wiki/Functional_group

    Functional groups can also be charged, e.g. in carboxylate salts (−COO −), which turns the molecule into a polyatomic ion or a complex ion. Functional groups binding to a central atom in a coordination complex are called ligands. Complexation and solvation are also caused by specific interactions of functional groups.

  9. Trimethyl borate - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_borate

    Trimethyl borate is the main precursor to sodium borohydride by its reaction with sodium hydride in the Brown-Schlesinger process: . 4 NaH + B(OCH 3) 3 → NaBH 4 + 3 NaOCH 3. It is a gaseous anti-oxidant in brazing and solder flux.