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1,2-Dimethylcyclopropane is a cycloalkane consisting of a cyclopropane ring substituted with two methyl groups attached to adjacent carbon atoms. [1] It has three stereoisomers , one cis -isomer and a pair of trans - enantiomers , which differ depending on the orientation of the two methyl groups.
[2] As of early 1990s, it was present in American [3] and European [4] gasoline in small amounts, and by 2011 its share in US gasoline varied between 1 and 3%. [5] It has a research octane number of 103 and motor octane number of 95. [6] The C 6 core of methylcyclopentane is not perfectly planar and can pucker to alleviate stress in its ...
C 5 H 10 is the molecular formula of 13 hydrocarbon isomers (represented by their CAS numbers on the chart). ... (R,R)-1,2-dimethylcyclopropane or (1R-trans) ...
Norbornane (also called bicyclo[2.2.1]heptane). Unsubstituted cycloalkanes that contain a single ring in their molecular structure are typically named by adding the prefix "cyclo" to the name of the corresponding linear alkane with the same number of carbon atoms in its chain as the cycloalkane has in its ring.
Cyclopentane is a minor component of automobile fuel, with its share in US gasoline varying between 0.2 and 1.6% in early 1990s [8] and 0.1 to 1.7% in 2011. [9] Its research and motor octane numbers are reported as 101 or 103 and 85 or 86 respectively.
Indexes used for labelling must be superscripted: R 1-CH 2-R 2 (not R 1-CH 2-R 2) Do not include English text in images: this prevents their reuse in other languages. Methyl groups should be denoted with “CH 3 ”, not “Me”, unless they are bound to a heteroatom (for example, “NMe 2 ”).
2,2-Dimethylpentane can form a clathrate hydrate with helper gas molecules. The type of clathrate formed is called "clathrate H". 2,2-Dimethylpentane was the first compound for which the structure was determined. The clathrate has 34 molecules of water per molecule, and also has xenon and hydrogen sulfide as helper molecules.