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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 ...
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)
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.
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.
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 ...
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.
Names of acyl groups of ribonucleoside monophosphates such as AMP (5′-adenylic acid), GMP (5′-guanylic acid), CMP (5′-cytidylic acid), and UMP (5′-uridylic acid) are adenylyl, guanylyl, cytidylyl, and uridylyl respectively. In phospholipids, the acyl group of phosphatidic acid is called phosphatidyl-. Finally, many saccharides are acylated.
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.