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  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. 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.

  4. Acetoxy group - Wikipedia

    en.wikipedia.org/wiki/Acetoxy_group

    Activated ester form of acetic acid, such as a N-hydroxysuccinimide ester, although this is not advisable due to higher costs and difficulties. [3] Acetic anhydride in the presence of base with a catalyst such as pyridine with a bit of DMAP added. [4]

  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. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    A major factor in determining the reactivity of acyl derivatives is leaving group ability, which is related to acidity. Weak bases are better leaving groups than strong bases; a species with a strong conjugate acid (e.g. hydrochloric acid) will be a better leaving group than a species with a weak conjugate acid (e.g. acetic acid).

  7. 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.

  8. Basic oxide - Wikipedia

    en.wikipedia.org/wiki/Basic_oxide

    A basic oxide, also called a base anhydride (meaning "base without water"), is usually formed in the reaction of oxygen with metals, especially alkali (group 1) and alkaline earth (group 2) metals. Both of these groups form ionic oxides that dissolve in water to form basic solutions of the corresponding metal hydroxide: Alkali metals (Group 1)

  9. Oleum - Wikipedia

    en.wikipedia.org/wiki/Oleum

    Oleum (Latin oleum, meaning oil), or fuming sulfuric acid, is a term referring to solutions of various compositions of sulfur trioxide in sulfuric acid, or sometimes more specifically to disulfuric acid (also known as pyrosulfuric acid).