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2,3-Dimethylbutane Skeletal formula of 2,3-dimethylbutane with some implicit hydrogens shown: Ball and stick model of 2,3-dimethylbutane: Names Preferred IUPAC name ...
The molecular formula C 6 H 14 (molar mass: 86.17 g/mol) may refer to: Dimethylbutanes 2,2-Dimethylbutane; 2,3-Dimethylbutane; Hexane; Methylpentanes 2-Methylpentane;
Dimethylbutane (DMB) may refer to: 2,2-Dimethylbutane; 2,3-Dimethylbutane; See also. Dimethylbutanol This page was last edited on 1 April 2021, at ...
For example, compare isobutane (2-methylpropane) and n-butane (butane), which boil at −12 and 0 °C, and 2,2-dimethylbutane and 2,3-dimethylbutane which boil at 50 and 58 °C, respectively. [ 18 ] On the other hand, cycloalkanes tend to have higher boiling points than their linear counterparts due to the locked conformations of the molecules ...
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. 2 R−X + 2 Na → R−R + 2 NaX. The reaction is of little value except for intramolecular versions, such as 1,6-dibromohexane + 2 Na → cyclohexane + 2 NaBr.
The general chemical formula of the halogen addition reaction is: C=C + X 2 → X−C−C−X (X represents the halogens bromine or chlorine, and in this case, a solvent could be CH 2 Cl 2 or CCl 4). The product is a vicinal dihalide. This type of reaction is a halogenation and an electrophilic addition.
[2] [5] The compound is used as a reactant in the synthesis of a number of compounds. Notably it is used to synthesize 2,3-dimethylbut-2-ene, and is then converted to 2,3-dimethylbutane-2,3-diol and methyl tert-butyl ketone, better known as pinacolone. Pinacolone itself is then used in synthesis for number of pesticides.
DMDNB, or also DMNB, chemically 2,3-dimethyl-2,3-dinitrobutane, is a volatile organic compound used as a detection taggant for explosives, mostly in the United States where it is virtually the only such taggant in use.