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An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).
α-Halo carboxylic acids and esters are organic compounds with the respective formulas RCHXCO 2 H and RCHXCO 2 R' where R and R' are organic substituents. The X in these compounds is a halide, usually chloride and bromide. These compounds are often used as intermediates in the preparation of more elaborate derivatives. They are often potent ...
An ester of a carboxylic acid. R stands for any group (typically hydrogen or organyl) and R ′ stands for any organyl group. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (R ′). [1]
In a related reaction, thioesters can be converted into esters. [9] Thioacetate esters can also be cleaved with methanethiol in the presence of stoichiometric base, as illustrated in the preparation of pent-4-yne-1-thiol: [10] H 3 C(CH 2) 3 OMs + KSAc → H 3 C(CH 2) 3 SAc + KOMs H 3 C(CH 2) 3 SAc + HSMe → H 3 C(CH 2) 3 SH + MeSAc
[10] [11] Acid anhydrides can be used in place of acid chloride. The reaction yields a 1:1 mixture of the homologated acid and the corresponding methyl ester. [12] This method can also be used with primary diazoalkanes, to produce secondary α-diazo ketones. However, there are many limitations.
Structure of thiosulfonate ester. Thiosulfonates are organosulfur compounds with the formula RSO 2 SR'. The parent member CH 3 SO 2 SCH 3 is a colorless liquid.. Thiosulfonate esters are usually produced by oxidation of disulfides or the nucleophilic attack of thiolates on organosulfonyl halides. [1]
Saponification is a process of cleaving esters into carboxylate salts and alcohols by the action of aqueous alkali. Typically aqueous sodium hydroxide solutions are used. [ 1 ] [ 2 ] It is an important type of alkaline hydrolysis .
Trimethyl borate is a popular borate ester used in organic synthesis. Borate esters form spontaneously when treated with diols such as sugars and the reaction with mannitol forms the basis of a titrimetric analytical method for boric acid. Metaborate esters show considerable Lewis acidity and can initiate epoxide polymerization reactions. [4]