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Cyclopentane is also used in the manufacture of synthetic resins and rubber adhesives. [citation needed] 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 ...
Because (1R,3R)-1,2,3-trimethylcyclopentane is a cycloalkane, its three methyl substituents are capable of exhibiting cis/trans isomerism. This implies that the methyl groups in positions 1,2, and 3 may occupy different spatial arrangements (i.e.they may either lay cis or trans with respect to each other).
Metallacyclopentanes are intermediates in the metal-catalysed dimerization, trimerization, and tetramerization of ethylene to give 1-butene, 1-hexene, and 1-octene, respectively. These compounds are of commercial interest as comonomers, used in the production of polyethylene. [6] Cyclopentane and metallacyclopentane The chromium-catalyzed ...
C 5 H 10 is the molecular formula of 13 hydrocarbon isomers (represented by their CAS numbers on the chart). They can be divided into cycloalkanes and alkenes . Cycloalkanes
1,2,3,4,5-Cyclopentanepentol, also named cyclopentane-1,2,3,4,5-pentol or 1,2,3,4,5-pentahydroxycyclopentane is a chemical compound with formula C 5 H 10 O 5 or (–CHOH–) 5, whose molecule consists of a ring of five carbon atoms (a cyclopentane skeleton), each connected to one hydrogen and one hydroxyl group. [1]
Original file (SVG file, nominally 53 × 50 pixels, file size: 1 KB) This is a file from the Wikimedia Commons . Information from its description page there is shown below.
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 structure. [7]
1,2-Cyclopentanedione is the organic compound with the formula (CH 2) 3 (CO) 2. It is one of two isomeric cyclopentanediones, the other being 1,3-cyclopentanedione . It was first prepared by base-induced condensation of di ethylglutarate with diethyloxalate , followed by hydrolysis of the resulting diketodiester followed by decarboxylation. [ 1 ]