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The carboxylic acid Schmidt reaction starts with acylium ion 1 obtained from protonation and loss of water. Reaction with hydrazoic acid forms the protonated azido ketone 2 , which goes through a rearrangement reaction with the alkyl group R, migrating over the C-N bond with expulsion of nitrogen.
A common reaction of metal carboxylates is their displacement by more basic ligands. Acetate is a common leaving group. They are especially prone to protonolysis, which is widely used to introduce ligands, displacing the carboxylic acid. In this way octachlorodimolybdate is produced from dimolybdenum tetraacetate:
Calconcarboxylic acid (IUPAC name 3-hydroxy-4-[(2-hydroxy-4-sulfonaphthalen-1-yl)diazenyl]naphthalene-2-carboxylic acid; commonly called Patton and Reeder's Indicator) is an azo dye that is used as an indicator for complexometric titrations of calcium with ethylenediaminetetraacetic acid (EDTA) in the presence of magnesium. [2]
Carboxylation is a chemical reaction in which a carboxylic acid is produced by treating a substrate with carbon dioxide. [1] The opposite reaction is decarboxylation.In chemistry, the term carbonation is sometimes used synonymously with carboxylation, especially when applied to the reaction of carbanionic reagents with CO 2.
For instance, the reaction of an carboxylic acid with amines to form a salt takes place with K of 10 5–6, and at ordinary temperatures, this process is regarded as irreversible. Yet, with sufficient heating, the reverse reaction takes place to allow formation of the tetrahedral intermediate and, ultimately, amide and water.
Such reactions usually involve an aqueous acidic workup, though this step is rarely shown in reaction schemes. In cases where the Grignard reagent is adding to an aldehyde or a prochiral ketone, the Felkin-Anh model or Cram's Rule can usually predict which stereoisomer will be formed.
The product selectivity and yield of catalytic reactions (e.g. cyclopropanation) have also been shown to be impacted by defective sites, such as Cu(I) or incompletely deprotonated carboxylic acid moities of the linkers. [23] MIL-101, a large-cavity MOF having the formula [Cr 3 F(H 2 O) 2 O(BDC) 3], is a cyanosilylation catalyst. [56]
An illustrative synthesis is the reaction of a cationic iron carbonyl with a stoichiometric amount of base: [2] [(C 5 H 5)(CO) 2 FeCO]BF 4 + NaOH → [(C 5 H 5)(CO) 2 FeCO 2 H + NaBF 4. When applied to simple metal carbonyls, this kind of conversion is sometimes called the Hieber base reaction. Decarboxylation of the resulting anion gives the ...