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  2. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde , ketone , or carboxylic acid ), then the prefix hydroxy- is used, [ 19 ] e.g., as in 1-hydroxy-2 ...

  3. Alkoxide - Wikipedia

    en.wikipedia.org/wiki/Alkoxide

    2 CH 3 OH + 2 Na → 2 CH 3 ONa + H 2. Other alkali metals can be used in place of sodium, and most alcohols can be used in place of methanol. Generally, the alcohol is used in excess and left to be used as a solvent in the reaction. Thus, an alcoholic solution of the alkali alkoxide is used.

  4. Hydroxy group - Wikipedia

    en.wikipedia.org/wiki/Hydroxy_group

    In chemistry, a hydroxy or hydroxyl group is a functional group with the chemical formulaOH and composed of one oxygen atom covalently bonded to one hydrogen atom. In organic chemistry , alcohols and carboxylic acids contain one or more hydroxy groups.

  5. 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).

  6. Ethanol - Wikipedia

    en.wikipedia.org/wiki/Ethanol

    Ethanol (also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound with the chemical formula CH 3 CH 2 OH. It is an alcohol, with its formula also written as C 2 H 5 OH, C 2 H 6 O or EtOH, where Et stands for ethyl. Ethanol is a volatile, flammable, colorless liquid with a characteristic wine-like ...

  7. Hydroxylamine - Wikipedia

    en.wikipedia.org/wiki/Hydroxylamine

    R 2 C=O + [NH 3 OH]Cl → R 2 C=N−OH + NaCl + H 2 O (in NaOH solution) This reaction is useful in the purification of ketones and aldehydes: if hydroxylamine is added to an aldehyde or ketone in solution, an oxime forms, which generally precipitates from solution; heating the precipitate with an inorganic acid then restores the original ...

  8. Diol - Wikipedia

    en.wikipedia.org/wiki/Diol

    The chemical reaction called Sharpless asymmetric dihydroxylation can be used to produce chiral diols from alkenes using an osmate reagent and a chiral catalyst. Another method is the Woodward cis-hydroxylation (cis diol) and the related Prévost reaction (anti diol), which both use iodine and the silver salt of a carboxylic acid.

  9. Hydroxide - Wikipedia

    en.wikipedia.org/wiki/Hydroxide

    The formula, Cu 2 CO 3 (OH) 2 shows that it is halfway between copper carbonate and copper hydroxide. Indeed, in the past the formula was written as CuCO 3 ·Cu(OH) 2. The crystal structure is made up of copper, carbonate and hydroxide ions. [37] The mineral atacamite is an example of a basic chloride. It has the formula, Cu 2 Cl(OH) 3.

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