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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

    In the Goldfinger mechanism, the purpose of the NBS is simply to maintain a very low concentration of molecular bromine, while in the Bloomfield mechanism, its purpose is the generation of the initial radical used in the reaction, [11] which again can be quite a difficult process. [12]

  4. 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 ...

  5. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    Substitution reactions in organic chemistry are classified either as electrophilic or nucleophilic depending upon the reagent involved, whether a reactive intermediate involved in the reaction is a carbocation, a carbanion or a free radical, and whether the substrate is aliphatic or aromatic. Detailed understanding of a reaction type helps to ...

  6. Bartoli indole synthesis - Wikipedia

    en.wikipedia.org/wiki/Bartoli_indole_synthesis

    The mechanism of the Bartoli indole synthesis. The mechanism begins by the addition of the Grignard reagent (2) onto the nitroarene (1) to form intermediate 3. Intermediate 3 spontaneously decomposes to form a nitrosoarene (4) and a magnesium salt (5). (Upon reaction workup, the magnesium salt will liberate a carbonyl compound (6).)

  7. Hydroamination - Wikipedia

    en.wikipedia.org/wiki/Hydroamination

    The mechanism of metal-catalyzed hydroamination has been well studied. [11] Particularly well studied is the organolanthanide catalyzed intramolecular hydroamination of alkenes. [23] First, the catalyst is activated by amide exchange, generating the active catalyst (i). Next, the alkene inserts into the Ln-N bond (ii). [24]

  8. Boomers are sad they may never be grandparents as fewer ... - AOL

    www.aol.com/finance/boomers-sad-may-never...

    The birth rate in America has long been on a decline, with the fertility rate reaching historic lows in 2023. More women between ages 25 to 44 aren’t having children, for a number of reasons.

  9. Jacobsen's catalyst - Wikipedia

    en.wikipedia.org/wiki/Jacobsen's_catalyst

    However, as is the case with the overall mechanism, the pathway of alkene approach is also debated. [8] One proposed substrate approach pathway - Note: Substrates are perpendicular to the plane of the catalyst. The ease with which Jacobsen's catalyst selectively epoxidizes cis-alkenes has been difficult to replicate with terminal and trans ...