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  2. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    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] 2 Li + C 4 H 9 X → C ...

  3. Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Butyl_bromide

    Butyl bromide (C 4 H 9 Br) may refer to: 1-Bromobutane (n-Butyl bromide) 2-Bromobutane (sec-butyl bromide) 1-Bromo-2-methylpropane (isobutyl bromide)

  4. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    In organic chemistry, butyl is a four-carbon alkyl radical or substituent group with general chemical formula −C 4 H 9, derived from either of the two isomers (n-butane and isobutane) of butane. The isomer n -butane can connect in two ways, giving rise to two "-butyl" groups:

  5. Bromobutane - Wikipedia

    en.wikipedia.org/wiki/Bromobutane

    2-Bromobutane (sec-butyl bromide or methylethylbromomethane) Index of chemical compounds with the same name This set index article lists chemical compounds articles associated with the same name.

  6. 2-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/2-Bromobutane

    Both compounds share the molecular formula C 4 H 9 Br. 2-Bromobutane is also known as sec-butyl bromide or methylethylbromomethane. Because it contains bromine, a halogen, it is part of a larger class of compounds known as alkyl halides. It is a colorless liquid with a pleasant odor.

  7. n-Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/N-Butylbenzene

    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. The synthesis of n-butylbenzene by the reaction of chlorobenzene and butylmagnesium bromide was one of the first demonstrations of the Kumada coupling using nickel diphosphine ...

  8. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    An example of a reaction taking place with an S N 1 reaction mechanism is the hydrolysis of tert-butyl bromide forming tert-butanol: This S N 1 reaction takes place in three steps: Formation of a tert-butyl carbocation by separation of a leaving group (a bromide anion) from the carbon atom: this step is slow. [5] Recombination of carbocation ...

  9. Sodium bromide - Wikipedia

    en.wikipedia.org/wiki/Sodium_bromide

    Sodium bromide is an inorganic compound with the formula Na Br. It is a high-melting white, crystalline solid that resembles sodium chloride . It is a widely used source of the bromide ion and has many applications.