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Since the longest continuous chain in isobutane contains only three carbon atoms, the preferred IUPAC name is 2-methylpropane but the locant (2-) is typically omitted in general nomenclature as redundant; C2 is the only position on a propane chain where a methyl substituent can be located without altering the main chain and forming the ...
Isobutane, also known as methylpropane or 2-methylpropane Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .
2 Structure and properties. 3 Thermodynamic properties. 4 Vapor pressure of liquid. 5 Spectral data. ... This page provides supplementary chemical data on isobutane.
If it connects at one of the non-terminal (internal) carbon atoms, it is secondary butyl or sec-butyl: −CH(CH 3)−CH 2 −CH 3 (preferred IUPAC name: butan-2-yl) The second isomer of butane, isobutane, can also connect in two ways, giving rise to two additional groups:
Isobutylene is used in the production of a variety of products. It is alkylated with butane to produce isooctane or dimerized to diisobutylene (DIB) and then hydrogenated to make isooctane, a fuel additive.
Names Preferred IUPAC name. 1-Chloro-2-methylpropane. Identifiers CAS Number. 513-36-0 ... It is a chlorinated derivative of isobutane. Synthesis
Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH 3) 2 CHCH 2 OH (sometimes represented as i-BuOH).This colorless, flammable liquid with a characteristic smell is mainly used as a solvent either directly or as its esters.
The main structure of chemical names according to IUPAC nomenclature. The International Union of Pure and Applied Chemistry (IUPAC) has published four sets of rules to standardize chemical nomenclature. There are two main areas: IUPAC nomenclature of inorganic chemistry (Red Book) IUPAC nomenclature of organic chemistry (Blue Book)