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3-Ethylpentane (C 7 H 16) is a branched saturated hydrocarbon. It is an alkane, and one of the many structural isomers of heptane, consisting of a five carbon chain with a two carbon branch at the middle carbon. An example of an alcohol derived from 3-ethylpentane is the tertiary alcohol 3-ethylpentan-3-ol. [3]
2-ethyl-3- methylbutanoic acid CH 3 CH(CH 3)CH(C 2 H 5)COOH C8. IUPAC name: Common name: Structural formula octanoic acid: caprylic acid: CH 3 (CH 2) 6 COOH
2-Phenylhexane is an aromatic hydrocarbon. It can be produced by a Friedel-Crafts alkylation between 1-chlorohexane and benzene ., [ 1 ] or by the reaction of benzene and 1-hexene with various acid catalysts such as antimony pentafluoride , [ 2 ] scandium(III) triflate , [ 3 ] and phosphoric acid .
The longest possible main alkane chain is used; therefore 3-ethyl-4-methylhexane instead of 2,3-diethylpentane, even though these describe equivalent structures. The di-, tri- etc. prefixes are ignored for the purpose of alphabetical ordering of side chains (e.g. 3-ethyl-2,4-dimethylpentane, not 2,4-dimethyl-3-ethylpentane).
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5.2 Dimethyl+ethyl. 5.3 Diethyl. Toggle the table of contents. List of isomers of nonane. 4 languages.
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2,4,5-Trimethoxyphenethylamine (2,4,5-TMPEA or TMPEA-2), also known as 2C-O or 2C-OMe, or is a phenethylamine of the 2C family and was first synthesized by Jansen in 1931. [1] It is a positional isomer of the drug mescaline (3,4,5-tri methoxy ).