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2-Bromobutane is relatively stable, but is toxic and flammable. When treated with a strong base, it is prone to undergo an E2 reaction, which is a bimolecular elimination reaction, resulting in (predominantly) 2-butene, an alkene (double bond). 2-Bromobutane is an irritant, and harmful if ingested. It can irritate and burn skin and eyes.
As a primary haloalkane, it is prone to S N 2 type reactions. It is commonly used as an alkylating agent. When combined with magnesium metal in dry ether, it gives the corresponding Grignard reagent. Such reagents are used to attach butyl groups to various substrates. 1-Bromobutane is the precursor to n-butyllithium: [4]
Butadiene is also useful in the synthesis of cycloalkanes and cycloalkenes, as it reacts with double and triple carbon-carbon bonds through Diels-Alder reactions. The most widely used such reactions involve reactions of butadiene with one or two other molecules of butadiene, i.e., dimerization and trimerization respectively.
Butene, also known as butylene, is an alkene with the formula C 4 H 8. The word butene may refer to any of the individual compounds. They are colourless gases that ...
The relative rates at which different halogens react vary considerably: [citation needed] fluorine (108) > chlorine (1) > bromine (7 × 10 −11) > iodine (2 × 10 −22).. Radical fluorination with the pure element is difficult to control and highly exothermic; care must be taken to prevent an explosion or a runaway reaction.
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. ...
A halogen addition reaction is a simple organic reaction where a halogen molecule is added to the carbon–carbon double bond of an alkene functional group. [1] 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 ...
Its main uses are in the production of high-octane gasoline (petrol) on alkylation units and butadiene, [4] although some but-2-ene is also used to produce the solvent butanone via hydration reaction to butan-2-ol followed by oxidation.