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It has the chemical formula (CH 3) 2 CHCH(CH 3) 2. It is a colorless liquid which boils at 57.9 °C. It is a colorless liquid which boils at 57.9 °C. References
Structural formula Acetic acid: ethanoic acid CH 3 CO 2 H Glycolic acid: hydroxyacetic acid ... HOOC(CH 2) 4 COOH 2,3-dimethylbutanoic acid CH 3 (CHCH 3) 2 COOH
2-Methylbutanoic acid, also known as 2-methylbutyric acid is a branched-chain alkyl carboxylic acid with the chemical formula CH 3 CH 2 CH(CH 3)CO 2 H, classified as a short-chain fatty acid. It exists in two enantiomeric forms, ( R )- and ( S )-2-methylbutanoic acid.
In May 2023, Desmos released a beta for a remade Geometry Tool. In it, geometrical shapes can be made, as well as expressions from the normal graphing calculator, with extra features. [ 8 ] In September 2023, Desmos released a beta for a 3D calculator, which added features on top of the 2D calculator, including cross products, partial ...
Symbolab is an answer engine [1] that provides step-by-step solutions to mathematical problems in a range of subjects. [2] It was originally developed by Israeli start-up company EqsQuest Ltd., under whom it was released for public use in 2011. In 2020, the company was acquired by American educational technology website Course Hero. [3] [4]
2,3-Dimethyl-1-butene is an organic compound with the formula CH 2 =C(CH 3)CH(CH 3) 2. Like the other isomers of dimethylbutene, it is a colorless liquid. Together with 2,3-dimethyl-2-butene it can be produced by dimerization of propylene. It is a precursor to the commercial fragrance tonalide. [1]
The molecular formula C 5 H 10 O 2 (molar mass: 102.13 g/mol) may refer to: tert-Butyl formate; Ethyl propionate; Hydroxypivaldehyde; Isobutyl formate; Isopropyl acetate; Methylbutanoic acids. 2-Methylbutanoic acid; 3-Methylbutanoic acid (isovaleric acid) Methyl butyrate; Methyl isobutyrate; Pivalic acid; Propyl acetate; Tetrahydrofurfuryl ...
For esters such as ethyl acetate (CH 3 COOCH 2 CH 3), ethyl formate (HCOOCH 2 CH 3) or dimethyl phthalate that are based on common acids, IUPAC recommends use of these established names, called retained names. The "-oate" changes to "-ate." Some simple examples, named both ways, are shown in the figure above.