What is the structural formula for 2 2-Dimethylbutane?
What is the structural formula for 2 2-Dimethylbutane?
(CH3)3CCH2CH3
2,2-Dimethylbutane/Formula
Which of the following is 2 2-Dimethylbutane?
2,2-Dimethylbutane, trivially known as neohexane, is an organic compound with formula C6H14 or (H3C-)3-C-CH2-CH3. It is therefore an alkane, indeed the most compact and branched of the hexane isomers — the only one with a quaternary carbon and a butane (C4) backbone.
What is the condensed structural formula for 2 2?
2,2-Dimethylbutane has a four-carbon chain with two methyl groups on C-2. The condensed structural formula is CH₃C(CH₃)₂CH₂CH₃.
What is the condensed structural formula for 2 3-Dimethylbutane?
2,3-Dimethylbutane | C6H14 – PubChem.
What is the formula for 2, 2 dimethylbutane?
2,2-Dimethylbutane From Wikipedia, the free encyclopedia 2,2-Dimethylbutane, trivially known as neohexane, is an organic compound with formula C 6 H 14 or (H 3 C-) 3 -C-CH 2 -CH 3. It is therefore an alkane, indeed the most compact and branched of the hexane isomers — the only one with a quaternary carbon and a butane (C 4) backbone.
What is the Henry’s Law constant for 2, 2-dimethylbutane?
The Henry’s Law constant for 2,2-dimethylbutane is estimated as 1.7 atm-cu m/mole(SRC) derived from its vapor pressure, 319 mm Hg(1), and water solubility, 21.2 mg/L (2). This Henry’s Law constant indicates that 2,2-dimethylbutane is expected to volatilize rapidly from water surfaces(3).
What is CID 6589 for 2, 3 dimethylbutane?
2,3-Dimethylbutane | C6H14 | CID 6589 – structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more. This application requires Javascript. Please turn on Javascript in order to use this application.
Where can I find dimethylbutane in the US?
New York, NY 2007., p. 880 121.5 °F at 760 mm Hg (NTP, 1992) National Toxicology Program, Institute of Environmental Health Sciences, National Institutes of Health (NTP). 1992. National Toxicology Program Chemical Repository Database. Research Triangle Park, North Carolina.