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n-Butylbenzene is the organic compound with the formula C 6 H 5 C 4 H 9. Of two isomers of butylbenzene, n -butylbenzene consists of a phenyl group attached to the 1 position of a butyl group. It is a slightly greasy, colorless liquid.
tert-Butylbenzene is an organic compound classified as an aromatic hydrocarbon. Its structure consists of a benzene ring substituted with a tert -butyl group . It is a flammable colorless liquid which is nearly insoluble in water but miscible with organic solvents.
Gattermann-Koch reaction: named after German chemists Ludwig Gattermann and Julius Arnold Koch, the Gattermann-Koch reaction is a catalyzed formylation of alkylbenzenes with carbon monoxide and hydrochloric acid. [5] Alkylbenzene sulfonation reaction: electrophilic addition of a sulfonic acid group onto the aromatic ring. [4]
sec-Butylbenzene is an organic compound classified as an aromatic hydrocarbon. Its structure consists of a benzene ring substituted with a sec -butyl group . It is a flammable colorless liquid which is nearly insoluble in water but miscible with organic solvents.
N-tert-Butylbenzenesulfinimidoyl chloride is a useful oxidant for organic synthesis reactions. [1] It is a good electrophile, and the sulfimide S=N bond can be attacked by nucleophiles, such as alkoxides, enolates, and amide ions. The nitrogen atom in the resulting intermediate is basic, and can abstract an α-hydrogen to create a new double bond.
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Potassium permanganate will decompose into potassium manganate, manganese dioxide and oxygen gas: 2 KMnO 4 → K 2 MnO 4 + MnO 2 + O 2. This reaction is a laboratory method to prepare oxygen, but produces samples of potassium manganate contaminated with MnO 2. The former is soluble and the latter is not.
Isobutylbenzene is a chemical compound with the molecular formula C 10 H 14. [2] It is used in chemical synthesis as a fuel and in pharmaceuticals. For instance, it is used to make pain killers like ibuprofen.