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  2. Fluorobenzene - Wikipedia

    en.wikipedia.org/wiki/Fluorobenzene

    PhF behaves rather differently from other halobenzene derivatives owing to the pi-donor properties of fluoride. For example, the para position is more activated than benzene toward electrophiles. For this reason, it can be converted to 1-bromo-4-fluorobenzene with relatively high efficiency. [3]

  3. Halobenzene - Wikipedia

    en.wikipedia.org/wiki/Halobenzene

    Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... Halobenzene may also refer to any of the monosubstituted halobenzenes: Fluorobenzene;

  4. Category:Halobenzene compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Halobenzene_compounds

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  5. Aryl halide - Wikipedia

    en.wikipedia.org/wiki/Aryl_halide

    For example, 2,4-dinitrochlorobenzene reacts in basic solution to give a phenol. Unlike in most other substitution reactions, fluoride is the best leaving group, and iodide the worst. [ 16 ] A 2018 paper indicates that this situation may actually be rather common, occurring in systems that were previously assumed to proceed via S N Ar mechanisms.

  6. PHF - Wikipedia

    en.wikipedia.org/wiki/PHF

    PHF is a three letter acronym meaning: Paired Helical Filaments , a term for aggregations of protein in the brain, in conditions such as Alzheimer's disease The Pakistan Hockey Federation , national governing body for field hockey

  7. Electrophilic halogenation - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_halogenation

    In organic chemistry, an electrophilic aromatic halogenation is a type of electrophilic aromatic substitution.This organic reaction is typical of aromatic compounds and a very useful method for adding substituents to an aromatic system.

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  9. Mesomeric effect - Wikipedia

    en.wikipedia.org/wiki/Mesomeric_effect

    The +M effect, also known as the positive mesomeric effect, occurs when the substituent is an electron donating group. The group must have one of two things: a lone pair of electrons, or a negative charge. In the +M effect, the pi electrons are transferred from the group towards the conjugate system, increasing the density of the system.

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