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Organic carbon compounds are far more numerous than inorganic carbon compounds. In general bonds of carbon with other elements are covalent bonds. Carbon is tetravalent but carbon free radicals and carbenes occur as short-lived intermediates. Ions of carbon are carbocations and carbanions are also short-lived. An important carbon property is ...
The structure of carbodicarbenes greatly resembles that of carbodiphosphoranes. [4] Computational data for a N-methyl-substituted carbodicarbene predicted a carbon-carbon bond with a length only marginally longer than a C=C bond in a typical allene at 1.358 Å (compared with 1.308 Å for allene), but with a significantly bent bond angle of 131.8° (compared to 180° for a standard linear ...
C 10 Cl 10 O: kepone: 143-50-0 C 10 F 8: perfluoronaphthalene: 313-72-4 C 10 F 14 O: perfluoroadamantanone: 141635-73-6 C 10 F 18: perfluorodecalin: 306-94-5 C 10 F 21 I: perfluorodecyl iodide: 423-62-1 C 10 H 4 Cl 8 O: oxychlordane: 26880-48-8 C 10 H 5 Cl 7: heptachlor: 76-44-8 C 10 H 5 Cl 7 O: heptachlor epoxide: 1024-57-3 C 10 H 5 Cu: copper ...
A comparison between the five platonic solids and the corresponding three platonic hydrocarbons. In organic chemistry, a Platonic hydrocarbon is a hydrocarbon whose structure matches one of the five Platonic solids, with carbon atoms replacing its vertices, carbon–carbon bonds replacing its edges, and hydrogen atoms as needed.
In organic chemistry, a cyclo[n]carbon (or simply cyclocarbon) is a chemical compound consisting solely of a number n of carbon atoms covalently linked in a ring. Since the compounds are composed only of carbon atoms, they are allotropes of carbon .
The IUPAC accepts the use of 'annulene nomenclature' in naming carbocyclic ring systems with 7 or more carbon atoms, using the name '[n]annulene' for the mancude hydrocarbon with n carbon atoms in its ring, [1] though in certain contexts (e.g., discussions of aromaticity for different ring sizes), smaller rings (n = 3 to 6) can also be ...
Glassy carbon or vitreous carbon is a class of non-graphitizing carbon widely used as an electrode material in electrochemistry, as well as for high-temperature crucibles and as a component of some prosthetic devices. It was first produced by Bernard Redfern in the mid-1950s at the laboratories of The Carborundum Company, Manchester, UK.
Adding the hydrogen ion to one carbon atom in the alkene creates a positive charge on the other carbon, forming a carbocation intermediate. The more substituted the carbocation, the more stable it is, due to induction and hyperconjugation. The major product of the addition reaction will be the one formed from the more stable intermediate.