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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]
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).
Ester group (blue) which defines polyesters. This diagram shows just one ester linkage per repeat unit. Polyester is a category of polymers that contain one or two ester linkages in every repeat unit of their main chain. [1] As a specific material, it most commonly refers to a type called polyethylene terephthalate (PET).
Once the aspartic ester is formed, it is basically a sterically hindered diamine and thus in polymer science terms is a Chain extender rather than a chain terminator. Chain extenders ( f = 2) and cross linkers ( f ≥ 3) are low molecular weight amine terminated compounds that play an important role in polyurea compounds, coatings , elastomers ...
In organic chemistry, a nitrate ester is an organic functional group with the formula R−ONO 2, where R stands for any organyl group. They are the esters of nitric acid and alcohols . A well-known example is nitroglycerin , which is not a nitro compound, despite its name.
Any −OH groups on the phosphates in these ester molecules may lose H + ions to form anions, again depending on the pH in a solution. In the biochemistry of living organisms, there are many kinds of (mono)phosphate, diphosphate, and triphosphate compounds (essentially esters ), many of which play a significant role in metabolism such as ...
A wax ester (WE) is an ester of a fatty acid and a fatty alcohol. Wax esters are the main components of three commercially important waxes: carnauba wax, candelilla wax, and beeswax. [1] Wax esters are formed by combining one fatty acid with one fatty alcohol: + ′ ′ +
Glycerol has three hydroxyl functional groups, which can be esterified with one, two, or three fatty acids to form mono-, di-, and triglycerides. [2] These structures vary in their fatty acid alkyl groups as they can contain different carbon numbers, different degrees of unsaturation, and different configurations and positions of olefins.