When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Oxyacid - Wikipedia

    en.wikipedia.org/wiki/Oxyacid

    When oxyacids are heated, many of them dissociate to water and the anhydride of the acid. In most cases, such anhydrides are oxides of nonmetals. For example, carbon dioxide, CO 2, is the anhydride of carbonic acid, H 2 CO 3, and sulfur trioxide, SO 3, is the anhydride of sulfuric acid, H 2 SO 4. These anhydrides react quickly with water and ...

  3. Catalytic oxidation - Wikipedia

    en.wikipedia.org/wiki/Catalytic_oxidation

    Catalytic oxidations are common in biology, especially since aerobic life subsists on energy obtained by oxidation of organic compounds by air. In contrast to the industrial processes, which are optimized for producing chemical compounds, energy-producing biological oxidations are optimized to produce energy.

  4. Acid anhydride - Wikipedia

    en.wikipedia.org/wiki/Acid_anhydride

    An acid anhydride is a type of chemical compound derived by the removal of water molecules from an acid. In organic chemistry, organic acid anhydrides contain the functional group −C(=O)−O−C(=O)−. Organic acid anhydrides often form when one equivalent of water is removed from two equivalents of an organic acid in a dehydration reaction.

  5. Organic acid anhydride - Wikipedia

    en.wikipedia.org/wiki/Organic_acid_anhydride

    A common type of organic acid anhydride is a carboxylic anhydride, where the parent acid is a carboxylic acid, the formula of the anhydride being (RC(O)) 2 O. Symmetrical acid anhydrides of this type are named by replacing the word acid in the name of the parent carboxylic acid by the word anhydride. [2] Thus, (CH 3 CO) 2 O is called acetic ...

  6. Carbonyl group - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_group

    A ketone compound containing a carbonyl group (C=O) In organic chemistry, a carbonyl group is a functional group with the formula C=O, composed of a carbon atom double-bonded to an oxygen atom, and it is divalent at the C atom.

  7. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    For example, the C–C bond in ethane has an energy barrier of only 12 kJ/mol (3 kcal/mol). [2] Once a nucleophile attacks and a tetrahedral intermediate is formed, the energetically favorable resonance effect is lost. This helps explain why amides are one of the least reactive acyl derivatives. [3]

  8. Oxalic acid - Wikipedia

    en.wikipedia.org/wiki/Oxalic_acid

    Oxalic acid is an organic acid with the systematic name ethanedioic acid and chemical formula HO−C(=O)−C(=O)−OH, also written as (COOH) 2 or (CO 2 H) 2 or H 2 C 2 O 4. It is the simplest dicarboxylic acid. It is a white crystalline solid that forms a colorless solution in water.

  9. Acidic oxide - Wikipedia

    en.wikipedia.org/wiki/Acidic_oxide

    Carbonic acid is an illustrative example of the Lewis acidity of an acidic oxide. CO 2 + 2OH − ⇌ HCO 3 − + OH − ⇌ CO 3 2− + H 2 O. This property is a key reason for keeping alkali chemicals well sealed from the atmosphere, as long-term exposure to carbon dioxide in the air can degrade the material.