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Bicyclo[1.1.0]butane is an organic compound with the formula C 4 H 6. It is a bicyclic molecule consisting of two cis-fused cyclopropane rings, and is a colorless and easily condensed gas. [1] Bicyclobutane is noted for being one of the most strained compounds that is isolatable on a large scale — its strain energy is estimated at 63.9 kcal ...
The bridged bicyclic norbornane, formally bicyclo[2.2.1]heptane The spirocyclic compound spiro[5.5]undecane DABCO (1,4-diazabicyclo[2.2.2]octane) is often incorrectly depicted with one skewed ethylene group for the sake of clarity. A bicyclic molecule (from bi 'two' and cycle 'ring') is a molecule that features two joined rings. [1]
The prefix consists of three numbers that are arranged in descending order, separated by dots: [2.2.1]. Before the numerical prefix is another prefix indicating the number of rings (e.g., "bicyclo+"). Thus, the name is bicyclo[2.2.1]heptane. Cycloalkanes as a group are also known as naphthenes, a term mainly used in the petroleum industry. [4]
Bicyclo[1.1.0]butane is the only C 4 H 6 alkane and has no alkane isomer. Tetrahedrane is the only C 4 H 4 alkane and also has no alkane isomer. Alkanes with more than three carbon atoms can be arranged in various ways, forming structural isomers .
Bicyclo[1.1.1]pentane is an organic compound, the simplest member of the bicyclic bridged compounds family. It is a hydrocarbon with formula C 5 H 8. The molecular structure consists of three rings of four carbon atoms each. Bicyclo[1.1.1]pentane is a highly strained molecule.
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Propalene, or bicyclo[1.1.0]buta-1,3-diene Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .
In organic chemistry, the Wurtz reaction, named after Charles Adolphe Wurtz, is a coupling reaction in which two alkyl halides are treated with sodium metal to form a higher alkane.