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The side chains are: an ethyl- at carbon 4, an ethyl- at carbon 8, and a butyl- at carbon 12. Note: the −O−CH 3 at carbon atom 15 is not a side chain, but it is a methoxy functional group. There are two ethyl- groups. They are combined to create, 4,8-diethyl. The side chains are grouped like this: 12-butyl-4,8-diethyl.
3-Ethyl-3-methylhexane; 3-Ethyl-4-methylhexane; Pentane. Isomers where pentane is the longest chain Tetramethyl. 2,2,3,3-Tetramethylpentane;
2,5-Dimethylhexane; 3,3-Dimethylhexane; 3,4-Dimethylhexane [Wikidata This page was last edited on 27 April 2022, at 16:52 (UTC). Text is available under the ...
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N-octane has 23 constitutional isomers. 8 of these isomers have one stereocenter; 3 of them have two stereocenters. (3S,4S)-3,4-Dimethylhexane (top left) and (3R,4R)-3,4-Dimethylhexane (top right) are non-superimposable mirror images, so they are chiral enantiomers.
2,2,3,3-Tetramethylbutane Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .
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C 4 alkanes and cycloalkanes (left to right): n-butane and isobutane are the two C 4 H 10 isomers; cyclobutane and methylcyclopropane are the two C 4 H 8 isomers. Bicyclo[1.1.0]butane is the only C 4 H 6 alkane and has no alkane isomer.