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  2. Tripotassium phosphate - Wikipedia

    en.wikipedia.org/wiki/Tripotassium_phosphate

    k3po4 Tripotassium phosphate has few industrial applications, however it is commonly used as a base in laboratory-scale organic chemistry. Being insoluble in organic solvents, it is an easily removed proton acceptor in organic synthesis .

  3. Phosphoric acid - Wikipedia

    en.wikipedia.org/wiki/Phosphoric_acid

    Ca 5 (PO 4) 3 OH + 5 H 2 SO 4 3 H 3 PO 4 + 5 CaSO 4 + H 2 O Ca 5 (PO 4) 3 F + 5 H 2 SO 4 3 H 3 PO 4 + 5 CaSO 4 + HF. Calcium sulfate (gypsum, CaSO 4) is a by-product, which is removed as phosphogypsum. The hydrogen fluoride (HF) gas is streamed into a wet (water) scrubber producing hydrofluoric acid.

  4. Potassium hydroxide - Wikipedia

    en.wikipedia.org/wiki/Potassium_hydroxide

    ca(oh) 2 + k 2 co 3 caco 3 + 2 koh Filtering off the precipitated calcium carbonate and boiling down the solution gives potassium hydroxide ("calcinated or caustic potash"). This method of producing potassium hydroxide remained dominant until the late 19th century, when it was largely replaced by the current method of electrolysis of ...

  5. Cannizzaro reaction - Wikipedia

    en.wikipedia.org/wiki/Cannizzaro_reaction

    2 C 6 H 5 CHO + KOH C 6 H 5 CH 2 OH + C 6 H 5 COOK. The process is a redox reaction involving transfer of a hydride from one substrate molecule to the other: one aldehyde is oxidized to form the acid, the other is reduced to form the alcohol. [3]

  6. Potassium periodate - Wikipedia

    en.wikipedia.org/wiki/Potassium_periodate

    Potassium periodate can be prepared by the oxidation of an aqueous solution of potassium iodate by chlorine and potassium hydroxide. [1]KIO 3 + Cl 2 + 2 KOH KIO 4 + 2 KCl + H 2 O

  7. Ullmann condensation - Wikipedia

    en.wikipedia.org/wiki/Ullmann_condensation

    C 6 H 5 NH 2 + ClC 6 H 4 CO 2 H + KOH C 6 H 5 N(H)−C 6 H 4 CO 2 H + KCl + H 2 O. A typical catalyst is formed from copper(I) iodide and phenanthroline. The reaction is an alternative to the Buchwald–Hartwig amination reaction. Aryl iodides are more reactive arylating agents than are aryl chlorides, following the usual pattern.

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  9. Dipotassium phosphate - Wikipedia

    en.wikipedia.org/wiki/Dipotassium_phosphate

    As a food additive, dipotassium phosphate is used in imitation dairy creamers, dry powder beverages, mineral supplements, and starter cultures. [2] It functions as an emulsifier, stabilizer and texturizer; it also is a buffering agent, and chelating agent especially for the calcium in milk products..