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  2. N-Bromosuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Bromosuccinimide

    NBS will react with alkenes 1 in aqueous solvents to give bromohydrins 2. The preferred conditions are the portionwise addition of NBS to a solution of the alkene in 50% aqueous DMSO, DME, THF, or tert-butanol at 0 °C. [3] Formation of a bromonium ion and immediate attack by water gives strong Markovnikov addition and anti stereochemical ...

  3. Wohl–Ziegler bromination - Wikipedia

    en.wikipedia.org/wiki/Wohl–Ziegler_bromination

    The generation of NBS radicals depicted in the Bloomfield mechanism has been shown to be far more difficult than imagined when it was proposed, which is why it has failed as a proper model throughout the years; however, evidence suggests that the Bloomfield mechanism is still acceptable for the oxidation of alcohols using NBS. [10] In the ...

  4. Grieco elimination - Wikipedia

    en.wikipedia.org/wiki/Grieco_elimination

    The Grieco elimination is an organic reaction describing the elimination reaction of an aliphatic primary alcohol through a selenide to a terminal alkene. [1] [2] It is named for Paul Grieco. The alcohol first reacts with o-nitrophenylselenocyanate and tributylphosphine to form a selenide via a nucleophilic substitution on the electron ...

  5. Nucleophilic aromatic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_aromatic...

    The following is the reaction mechanism of a nucleophilic aromatic substitution of 2,4-dinitrochlorobenzene (1) in a basic solution in water. Nucleophilic aromatic substitution Since the nitro group is an activator toward nucleophilic substitution, and a meta director, it is able to stabilize the additional electron density (via resonance) when ...

  6. Hydroboration - Wikipedia

    en.wikipedia.org/wiki/Hydroboration

    This chemical reaction is useful in the organic synthesis of organic compounds. [1] Hydroboration produces organoborane compounds that react with a variety of reagents to produce useful compounds, such as alcohols, amines, or alkyl halides. The most widely known reaction of the organoboranes is oxidation to produce alcohols from alkenes.

  7. Hydroboration–oxidation reaction - Wikipedia

    en.wikipedia.org/wiki/Hydroboration–oxidation...

    Hydroboration–oxidation reaction is a two-step hydration reaction that converts an alkene into an alcohol. [1] The process results in the syn addition of a hydrogen and a hydroxyl group where the double bond had been. Hydroboration–oxidation is an anti-Markovnikov reaction, with

  8. Dying To Be Free - The Huffington Post

    projects.huffingtonpost.com/dying-to-be-free...

    The public began paying attention the following month, when Philip Seymour Hoffman died from an overdose of heroin and other drugs. His death followed that of actor Cory Monteith, who died of an overdose in July 2013 shortly after a 30-day stay at an abstinence-based treatment center.

  9. Olefin metathesis - Wikipedia

    en.wikipedia.org/wiki/Olefin_metathesis

    In any of the pairwise mechanisms with olefin pairing as rate-determining step this compound, a secondary reaction product of C12 with C6, would form well after formation of the two primary reaction products C12 and C16. In 1974 Casey was the first to implement carbenes into the metathesis reaction mechanism: [27]