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  2. Hydroxy group - Wikipedia

    en.wikipedia.org/wiki/Hydroxy_group

    In chemistry, a hydroxy or hydroxyl group is a functional group with the chemical formula −OH 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.

  3. Hydroxide - Wikipedia

    en.wikipedia.org/wiki/Hydroxide

    L n M(OH 2) + B ⇌ L n M(OH) + BH + (L = ligand, B = base) Vanadic acid H 3 VO 4 shows similarities with phosphoric acid H 3 PO 4 though it has a much more complex vanadate oxoanion chemistry. Chromic acid H 2 CrO 4, has similarities with sulfuric acid H 2 SO 4; for example, both form acid salts A + [HMO 4] −. Some metals, e.g. V, Cr, Nb, Ta ...

  4. 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-propanone (CH ...

  5. Base (chemistry) - Wikipedia

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

    A strong base is a basic chemical compound that can remove a proton (H +) from (or deprotonate) a molecule of even a very weak acid (such as water) in an acidbase reaction. Common examples of strong bases include hydroxides of alkali metals and alkaline earth metals, like NaOH and Ca(OH)

  6. Hydroxyl radical - Wikipedia

    en.wikipedia.org/wiki/Hydroxyl_radical

    The hydroxyl radical can damage virtually all types of macromolecules: carbohydrates, nucleic acids , lipids (lipid peroxidation) and amino acids (e.g. conversion of Phe to m-Tyrosine and o-Tyrosine). The hydroxyl radical has a very short in vivo half-life of approximately 10 −9 seconds and a high reactivity. [5]

  7. Hydroxylation - Wikipedia

    en.wikipedia.org/wiki/Hydroxylation

    2R 3 C−H + O 2 → 2 R 3 C−OH R 3 C−H + O 2 + 2e − + 2H + → R 3 C−OH + H 2 O. Since O 2 itself is a slow and unselective hydroxylating agent, catalysts are required to accelerate the pace of the process and to introduce selectivity. [1] Hydroxylation is often the first step in the degradation of organic compounds in air.

  8. Metal hydroxide - Wikipedia

    en.wikipedia.org/wiki/Metal_hydroxide

    In chemistry, metal hydroxides are a family of compounds of the form M n+ (OH) n, where M is a metal. They consist of hydroxide (OH −) anions and metallic cations, [1] and are often strong bases. Some metal hydroxides, such as alkali metal hydroxides, ionize completely when dissolved.

  9. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    The acidity of the hydroxyl group in phenols is commonly intermediate between that of aliphatic alcohols and carboxylic acids (their pK a is usually between 10 and 12). Deprotonation of a phenol forms a corresponding negative phenolate ion or phenoxide ion , and the corresponding salts are called phenolates or phenoxides ( aryloxides according ...