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Butane (/ ˈ b juː t eɪ n /) is an alkane with the formula C 4 H 10. Butane exists as two isomers, n -butane with connectivity CH 3 CH 2 CH 2 CH 3 and iso-butane with the formula (CH 3 ) 3 CH . Both isomers are highly flammable, colorless, easily liquefied gases that quickly vaporize at room temperature and pressure.
The following is a list of straight-chain alkanes, the total number of isomers of each ... C 4 H 10: n-butane: butyl hydride; methylethyl methane 5 3 3 C 5 H 12: n ...
Isobutane, also known as i-butane, 2-methylpropane or methylpropane, is a chemical compound with molecular formula HC(CH 3) 3. It is an isomer of butane . Isobutane is a colorless, odorless gas.
The isomer n-butane can connect in two ways, giving rise to two "-butyl" groups: If it connects at one of the two terminal carbon atoms, it is normal butyl or n-butyl: −CH 2 −CH 2 −CH 2 −CH 3 (preferred IUPAC name: butyl) If it connects at one of the non-terminal (internal) carbon atoms, it is secondary butyl or sec-butyl: −CH(CH 3 ...
Functional isomers are structural isomers which have different functional groups, resulting in significantly different chemical and physical properties. [ 11 ] An example is the pair propanal H 3 C–CH 2 –C(=O)-H and acetone H 3 C–C(=O)–CH 3 : the first has a –C(=O)H functional group, which makes it an aldehyde , whereas the second has ...
For example, in living organisms, the open-chain isomer of glucose usually exists only transiently, in small amounts; D-glucose is the usual isomer; and L-glucose is rare. Straight-chain molecules are often not literally straight, in the sense that their bond angles are often not 180°, but the name reflects that they are schematically straight.
sec-Butylamine is one of the four isomeric amines of butane, the others being n-butylamine, tert-butylamine, and isobutylamine. sec-Butylamine is chiral and therefore can exist in either of two enantiomeric forms. sec-Butylamine is used in the production of some pesticides. [2] Bromacil, a commercial herbicide, is produced from sec-butylamine. [3]
Discounting isomers that are equivalent under rotations, there are nine isomers that differ by this criterion, and behave as different stable substances (two of them being enantiomers of each other). The most common one in nature ( myo -inositol) has the hydroxyls on carbons 1, 2, 3 and 5 on the same side of that plane, and can therefore be ...