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IUPAC name: Common name: Structural formula octanoic acid: caprylic acid: CH 3 (CH 2) 6 COOH benzene-1,2-dicarboxylic acid: phthalic acid: C 6 H 4 (COOH) 2: benzene-1,3-dicarboxylic acid: isophthalic acid: C 6 H 4 (COOH) 2: benzene-1,4-dicarboxylic acid: terephthalic acid: C 6 H 4 (COOH) 2: 2-methylheptanoic acid C 5 H 11 CH(CH 3)COOH 3 ...
In organic chemistry, a methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms, having chemical formula CH 3 (whereas normal methane has the formula CH 4). In formulas, the group is often abbreviated as Me. This hydrocarbon group occurs in many organic compounds. It is a very stable group in ...
Ethane (US: / ˈ ɛ θ eɪ n / ETH-ayn, UK: / ˈ iː-/ EE-) is a naturally occurring organic chemical compound with chemical formula C 2 H 6. At standard temperature and pressure, ethane is a colorless, odorless gas. Like many hydrocarbons, ethane is isolated on an industrial scale from natural gas and as a petrochemical by-product of petroleum ...
The trivial names for simple ethers (i.e., those with none or few other functional groups) are a composite of the two substituents followed by "ether". For example, ethyl methyl ether (CH 3 OC 2 H 5), diphenylether (C 6 H 5 OC 6 H 5). As for other organic compounds, very common ethers acquired names before rules for nomenclature were formalized.
The conversion of methyl acetate back into its components, by an acid, is a first-order reaction with respect to the ester. The reaction of methyl acetate and a base, for example sodium hydroxide, is a second-order reaction with respect to both reactants. Methyl acetate is a Lewis base that forms 1:1 adducts with a variety of Lewis acids.
Methyl radical is an organic compound with the chemical formula CH • 3 (also written as [CH 3] •). It is a metastable colourless gas, which is mainly produced in situ as a precursor to other hydrocarbons in the petroleum cracking industry. It can act as either a strong oxidant or a strong reductant, and is quite corrosive to metals.
If the structure of the acid and the acid chloride are different, the product is a mixed anhydride. First, the carboxylic acid attacks the acid chloride ( 1 ) to give tetrahedral intermediate 2 . The tetrahedral intermediate collapses, ejecting chloride ion as the leaving group and forming oxonium species 3 .
Trimethylamine (TMA) is an organic compound with the formula N(CH 3) 3.It is a trimethylated derivative of ammonia.TMA is widely used in industry. [5] [6] At higher concentrations it has an ammonia-like odor, and can cause necrosis of mucous membranes on contact. [7]