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Linolelaidic acid is an omega-6 trans fatty acid (TFA) and is a cis–trans isomer of linoleic acid.It is found in partially hydrogenated vegetable oils. It is a white (or colourless) viscous liquid.
Transesterification is the process of exchanging the organic functional group R″ of an ester with the organic group R' of an alcohol. These reactions are often catalyzed by the addition of an acid or base catalyst. [1] Strong acids catalyze the reaction by donating a proton to the carbonyl group, thus making it a more potent electrophile.
Crotonic acid has 4 carbons, is included in croton oil, and is a trans-2-mono-unsaturated fatty acid.C 3 H 5 CO 2 H, IUPAC organization name (E)-but-2-enoic acid, trans-but-2-enoic acid, numerical representation 4:1, n-1, molecular weight 86.09, melting point 72–74 °C, boiling point 180–181 °C, specific gravity 1.027.
Rumenic acid, (9Z,11E)-9,11-octadecadienoic acid Index of chemical compounds with the same name This set index article lists chemical compounds articles associated with the same name.
It is a fatty acid sometimes denoted 18:2 (n−6) or 18:2 cis-9,12. A linoleate is a salt or ester of this acid. [5] Linoleic acid is a polyunsaturated, omega−6 fatty acid. It is a colorless liquid that is virtually insoluble in water but soluble in many organic solvents. [2] It typically occurs in nature as a triglyceride (ester of glycerin ...
Decadienoic acids with the two double bonds in the same positions can be further distinguished by the geometry of the adjacent single bonds. Each double bond that is adjacent to two single C–C bonds can be in two cis-trans conformations, namely with those two single bonds on the same side (cis or Z) or opposite sides (trans or E) of the double bond's plane.
(9Z,11E,13E)-Octadeca-9,11,13-trienoic acid (α-eleostearic acid). An octadecatrienoic acid is a chemical compound with formula C 18 H 30 O 2, a polyunsaturated fatty acid whose molecule has an 18-carbon unbranched backbone with three double bonds.
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).