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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. Potentially Hazardous Food - Wikipedia

    en.wikipedia.org/wiki/Potentially_Hazardous_Food

    Potentially Hazardous Food has been redefined by the US Food and Drug Administration in the 2013 FDA Food Code to Time/Temperature Control for Safety Food. [1] Pages 22 and 23 (pdf pages 54 and 55), state the following: PHF table A 2013 FDA Food Code. PHF table B 2013 FDA Food Code.

  4. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    1.67 –94.8 K b [3] Benzene: 0.87 80.1 2.65 5.5 ... [1] Water: 100.00 0.512 0.00 –1.86 ... [23] Pyridine: 115.3 [24] Dimethylacetamide: 166.1

  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. Halocarbon - Wikipedia

    en.wikipedia.org/wiki/Halocarbon

    Some haloalkanes are still widely used for industrial cleaning, such as methylene chloride (dichloromethane), and as refrigerants, such as R-134a (1,1,1,2-tetrafluoroethane). Haloalkenes have also been used as solvents , including perchloroethylene (Perc, tetrachloroethene), widespread in dry cleaning, and trichloroethylene (TCE, 1,1,2 ...

  7. Mesomeric effect - Wikipedia

    en.wikipedia.org/wiki/Mesomeric_effect

    In chemistry, the mesomeric effect (or resonance effect) is a property of substituents or functional groups in a chemical compound. It is defined as the polarity produced in the molecule by the interaction of two pi bonds or between a pi bond and lone pair of electrons present on an adjacent atom. [ 1 ]

  8. Neurofibrillary tangle - Wikipedia

    en.wikipedia.org/wiki/Neurofibrillary_tangle

    Neurofibrillary tangles are formed by hyperphosphorylation of a microtubule-associated protein known as tau, causing it to aggregate, or group, in an insoluble form.(These aggregations of hyperphosphorylated tau protein are also referred to as PHF, or "paired helical filaments").

  9. Polyhydroxyalkanoates - Wikipedia

    en.wikipedia.org/wiki/Polyhydroxyalkanoates

    Poly (HA MCL) from hydroxy fatty acids with medium chain lengths including six to 14 carbon atoms, can be made for example, by Pseudomonas putida. A few bacteria, including Aeromonas hydrophila and Thiococcus pfennigii , synthesize copolyester from the above two types of hydroxy fatty acids, or at least possess enzymes that are capable of part ...

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