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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. 2-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/2-Bromopropane

    Short-chain alkyl halides are often carcinogenic.. The bromine atom is at the secondary position, which allows the molecule to undergo dehydrohalogenation easily to give propene, which escapes as a gas and can rupture closed reaction vessels.

  4. Bromomethane - Wikipedia

    en.wikipedia.org/wiki/Bromomethane

    In Australia, bromomethane is the preferred fumigant of the Department of Agriculture and Water Resources for most organic goods imported into Australia. [12] The department conducts methyl bromide fumigation certification for both domestic and foreign fumigators who can then fumigate containers destined for Australia.

  5. Electrophile - Wikipedia

    en.wikipedia.org/wiki/Electrophile

    When water (H 2 O) is added and the mixture heated, ethanol (C 2 H 5 OH) is produced. The "spare" hydrogen atom from the water goes into "replacing" the "lost" hydrogen and, thus, reproduces sulfuric acid. Another pathway in which water molecule combines directly to the intermediate carbocation (lower way) is also possible.

  6. 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]

  7. Vinyl bromide - Wikipedia

    en.wikipedia.org/wiki/Vinyl_bromide

    Solubility in water. Insoluble log P: 1.57 ... Synthesis, reactions, and applications ... Bromoethane; References

  8. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    For example, the synthesis of macrocidin A, a fungal metabolite, involves an intramolecular ring closing step via an S N 2 reaction with a phenoxide group as the nucleophile and a halide as the leaving group, forming an ether. [2] Reactions such as this, with an alkoxide as the nucleophile, are known as the Williamson ether synthesis.

  9. Organic synthesis - Wikipedia

    en.wikipedia.org/wiki/Organic_synthesis

    Organic compounds are molecules consisting of combinations of covalently-linked hydrogen, carbon, oxygen, and nitrogen atoms. Within the general subject of organic synthesis, there are many different types of synthetic routes that can be completed including total synthesis, [1] stereoselective synthesis, [2] automated synthesis, [3] and many ...