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cyclopropane |
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cyclopropane, C3H6, a gaseous hydrocarbon. It is a cyclic alkane, its three carbon atoms being joined together in a ring. The angle between successive carbon-carbon bonds in the ring is only 60°, much less than that between successive carbon-carbon bonds in a normal open-chain alkane; the cyclopropane molecule is thus said to be "strained." Many reactions of cyclopropane involve breaking one of the carbon-carbon bonds in the ring, which opens the ring and relieves the strain. Cyclopropane is prepared commercially by the reaction of 1,3-dichloropropane with zinc. It is a potent inhalation anesthetic, that once enjoyed wide use, but has been replaced by less combustible gases. Cyclopropane allowed the transport of more oxygen to the tissues than did other common anesthetics and also produced greater skeletal muscle relaxation. It is not irritating to the respiratory tract. Because of the low solubility of cyclopropane in the blood, postoperative recovery was usually rapid but nausea and vomiting were common. See anesthesia anesthesia (ănĭsthē`zhə) [Gr. ..... Click the link for more information. . cyclopropane [¦sī·klō′prō‚pān] (organic chemistry) C3H6A colorless gas, insoluble in water; used as an anesthetic. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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164 LOWENTHAL RE,TETRAHEDR L,vol 0031,page 6005,1990,cites= 35,ASYMMETRIC CATALYTIC CYCLOPROPANATION OF OLEFINS - BIS-OXAZOLINE COPPER-COMPLEXES GC/MS AND RODIUM (II) CRABOXYLATE CATALYZED CYCLOPROPANATION IN UNDERGRADUATE ORGANIC CHEMISTRY LABORATORY. Yi Yuan commenced his study of asymmetric cyclopropanation and epoxidation of unfunctionalized olefins at Colorado State University, notably ranked among America's top national universities for academic achievement, quality of education, and value by U. |
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