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Bromobutane (molecular formula: C 4 H 9 Br, molar mass: 137.02 g/mol) may refer to either of two chemical compounds: 1-Bromobutane (n-butyl bromide)
Number of isomers [3] [4] Number of isomers including stereoisomers [3] [5] Molecular Formula Name of straight chain Synonyms 1 1 1 CH 4: methane: methyl hydride; natural gas 2 1 1 C 2 H 6: ethane: dimethyl; ethyl hydride; methyl methane 3 1 1 C 3 H 8: propane: dimethyl methane; propyl hydride 4 2 2 C 4 H 10: n-butane: butyl hydride ...
C 4 H 4 isomers with CAS registry numbers. Hydrocarbons that include four atoms are: butane C 4 H 10; isobutane C 4 H 10; but-1-ene C 4 H 8; but-2-ene C 4 H 8; but-1-yne C 4 H 6; but-2-yne C 4 H 6; isobutylene C 4 H 8; butadiene C 4 H 6; 1,2-butadiene C 4 H 6; vinylacetylene C 4 H 4; diacetylene C 4 H 2; butatriene C 4 H 4; cyclobutane C 4 H 8 ...
When oxygen is plentiful, butane undergoes complete combustion to form carbon dioxide and water vapor; when oxygen is limited, due to incomplete combustion, carbon or carbon monoxide may be formed instead of carbon dioxide. Butane is denser than air. When there is sufficient oxygen: 2 C 4 H 10 + 13 O 2 → 8 CO 2 + 10 H 2 O. When oxygen is limited:
2 Li + C 4 H 9 X → C 4 H 9 Li + LiX where X = Cl, Br. The lithium for this reaction contains 1-3% sodium. When bromobutane is the precursor, the product is a homogeneous solution, consisting of a mixed cluster containing both LiBr and LiBu. 1-Fluorobutane can be obtained by reacting 1-bromobutane with potassium fluoride in ethylene glycol. [5]
The carbon atom lies at or near the apex of a square pyramid with the other four groups at the corners. [7] [8] The simplest examples of organic molecules displaying inverted tetrahedral geometry are the smallest propellanes, such as [1.1.1]propellane; or more generally the paddlanes, [9] and pyramidane ([3.3.3.3]fenestrane).
The distannene (Me 3 Si) 2 CHSn=SnCH(SiMe 3) 2 has a tin-tin bond length just a little shorter than a single bond, a trans bent structure with pyramidal coordination at each tin atom, and readily dissociates in solution to form (Me 3 Si) 2 CHSn: (stannanediyl, a carbene analog). The bonding comprises two weak donor acceptor bonds, the lone pair ...
There are many oxides of carbon , of which the most common are carbon dioxide (CO 2) and carbon monoxide (CO). Other less known oxides include carbon suboxide (C 3 O 2) and mellitic anhydride (C 12 O 9). [5] There are also numerous unstable or elusive oxides, such as dicarbon monoxide (C 2 O), oxalic anhydride (C 2 O 4), and carbon trioxide (CO 3).