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  2. Bromoethane - Wikipedia

    en.wikipedia.org/wiki/Bromoethane

    Bromoethane, also known as ethyl bromide, is a chemical compound of the haloalkanes group. It is abbreviated by chemists as EtBr (which is also used as an abbreviation for ethidium bromide ). This volatile compound has an ether-like odor.

  3. Vinyl bromide - Wikipedia

    en.wikipedia.org/wiki/Vinyl_bromide

    Key: INLLPKCGLOXCIV ... Synthesis, reactions, and applications. It is produced from ethylene dibromide: CH 2 Br−CH 2 Br → CH 2 =CHBr + HBr. ... Bromoethane ...

  4. Bromoform - Wikipedia

    en.wikipedia.org/wiki/Bromoform

    Bromoform was discovered in 1832 by Löwig who distilled a mixture of bromal and potassium hydroxide, as analogous to preparation of chloroform from chloral. [5]Bromoform can be prepared by the haloform reaction using acetone and sodium hypobromite, by the electrolysis of potassium bromide in ethanol, or by treating chloroform with aluminium bromide.

  5. Dibromomethane - Wikipedia

    en.wikipedia.org/wiki/Dibromomethane

    Dibromomethane is used as a solvent, gauge fluid, and in organic synthesis (often as 1 H-NMR internal standard). [3] It conviently converts polyols (such as catechols) to their methylenedioxy derivatives, and bromomethylenates enolates. It is a much cheaper precursor to a Simmons-Smith-type reagent than diiodomethane. [5]

  6. Ethylmagnesium bromide - Wikipedia

    en.wikipedia.org/wiki/Ethylmagnesium_bromide

    Apart from acting as the synthetic equivalent of an ethyl anion synthon for nucleophilic addition, ethylmagnesium bromide may be used as a strong base to deprotonate various substrates such as alkynes: [1]

  7. Phenylmagnesium bromide - Wikipedia

    en.wikipedia.org/wiki/Phenylmagnesium_bromide

    Phenylmagnesium bromide is a strong nucleophile as well as a strong base.It can abstract even mildly acidic protons, thus the substrate must be protected where necessary. It often adds to carbonyls, such as ketones, aldehyde

  8. 1-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopropane

    The latter reaction is also viable laboratory synthesis. One laboratory technique for substitutive bromination treats propanol with a mixture of hydrobromic and sulfuric acids: CH 3 CH 2 CH 2 OH + HBr → CH 3 CH 2 CH 2 Br + H 2 O. Alternate synthetic routes include treating propanol with phosphorus tribromide [4] or via a Hunsdiecker reaction ...

  9. Bromomethane - Wikipedia

    en.wikipedia.org/wiki/Bromomethane

    Bromomethane, commonly known as methyl bromide, is an organobromine compound with formula C H 3 Br.This colorless, odorless, nonflammable gas is produced both industrially and biologically.