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3-Ethyl-2-methylhexane; 4-Ethyl-2-methylhexane; 3-Ethyl-3-methylhexane; 3-Ethyl-4-methylhexane; Pentane. Isomers where pentane is the longest chain Tetramethyl
Tetraethoxymethane can be used as a solvent and for the alkylation of CH-acidic compounds (e.g. phenols and carboxylic acids).In addition, it reacts with amines, enol ethers and sulfonamides, [12] whereby spiro compounds can also be obtained.
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).
Methylhexane may refer to either of two chemical compounds: 2-Methylhexane; 3-Methylhexane This page was last edited on 16 May 2022, at 14:52 (UTC). Text is ...
3-Methylhexane is a branched hydrocarbon with two enantiomers. [2] It is one of the isomers of heptane. The molecule is chiral, and is one of the two isomers of heptane to have this property, the other being its structural isomer 2,3-dimethylpentane. The enantiomers are (R)-3-methylhexane [3] and (S)-3-methylhexane. [4]
Methoxyethane, also known as ethyl methyl ether, is a colorless gaseous ether with the formula CH 3 OCH 2 CH 3. Unlike the related dimethyl ether and diethyl ether, which are widely used and studied, this mixed alkyl ether has no current applications. It is a structural isomer of isopropyl alcohol.
The structure of a typical methoxy group. In organic chemistry, a methoxy group is the functional group consisting of a methyl group bound to oxygen.This alkoxy group has the formula R−O−CH 3.
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