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Isobutylene (or 2-methylpropene) is a hydrocarbon with the chemical formula (CH 3) 2 C=CH 2. It is a four-carbon branched alkene (olefin), one of the four isomers of butylene . It is a colorless flammable gas, and is of considerable industrial value.
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.
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.
Anti-Markovnikov behaviour extends to more chemical reactions than additions to alkenes. Anti-Markovnikov behaviour is observed in the hydration of phenylacetylene by auric catalysis, which gives acetophenone; although with a special ruthenium catalyst [8] it provides the other regioisomer 2-phenylacetaldehyde: [9] Anti-Markovnikov hydration
MeO 2 CCH 2 CH 3 + CH 2 O → MeO 2 CCH(CH 2 OH)CH 3 MeO 2 CCH(CH 2 OH)CH 3 → MeO 2 CC(=CH 2)CH 3. Methyl propionate is used as a solvent for cellulose nitrate and lacquers, and as a raw material for the production of paints, varnishes and other chemicals such as methyl methacrylate. [2] [3] Due to its fruity smell and taste, it is also used ...
tert-Butyl bromide (also referred to as 2-bromo-2-methylpropane) is an organic compound with the formula Me 3 CBr (Me = methyl). The molecule features a tert-butyl group attached to a bromide substituent. This organobromine compound is used as a standard reagent in synthetic organic chemistry. It is a colorless liquid.
The Koch reaction is an organic reaction for the synthesis of tertiary carboxylic acids from alcohols or alkenes and carbon monoxide.Some commonly industrially produced Koch acids include pivalic acid, 2,2-dimethylbutyric acid and 2,2-dimethylpentanoic acid. [1]
Isoprenol is produced by the reaction between isobutene (2-methylpropene) and formaldehyde, in what is arguably the simplest example of the Prins reaction. The reaction of isobutene with formaldehyde to give isoprenol, the first step in the industrial manufacture of prenol.