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Although slower reacting than acid chlorides, anhydrides react with water to form carboxylic acids, with alcohols to form esters, and with amines to form amides. Anhydrides can also be reduced to 1 o alcohols by hydride reduction.
23 Ιαν 2023 · This page looks at the reactions of acid anhydrides with water, alcohols and phenols (including the manufacture of aspirin). These reactions are all considered together because their chemistry is so similar.
Acid chlorides react with carboxylic acids to form anhydrides as shown in the reaction below. Some cyclic anhydrides can be synthesized from the corresponding dicarboxylic acid with gentle heating. The example below shows the reaction of glutaric acid to form a cyclic anhydride.
Reactions of Acid Anhydrides. The chemistry of acid anhydrides is similar to that of acid chlorides, although anhydrides react more slowly. Thus, acid anhydrides react with water to form acids, with alcohols to form esters, with amines to form amides, and with LiAlH 4 to form primary alcohols.
Acid anhydrides are made from two carboxylic acid groups joined together. To form an acid anhydride, a water molecule is lost in a condensation reaction between two carboxylic acids. This is why acid anhydrides are called anhydride – lack of water.
The reactions (of both acyl chlorides and acid anhydrides) involve things like water, alcohols and phenols, or ammonia and amines. All of these particular cases contain a very electronegative element with an active lone pair of electrons - either oxygen or nitrogen.
This page looks at the reactions of acid anhydrides with water, alcohols and phenols (including the manufacture of aspirin). These reactions are all considered together because their chemistry is so similar.
