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  2. Dealkalization of water - Wikipedia

    en.wikipedia.org/wiki/Dealkalization_of_water

    Chloride cycle dealkalizers operate similar to sodium cycle cation water softeners. Like water softeners, dealkalizers contain ion-exchange resins that are regenerated with a concentrated salt solution - NaCl. In the case of a water softener, the cation exchange resin is exchanging sodium (the Na + ion of NaCl) for hardness minerals such as ...

  3. Acyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acyl_chloride

    In organic chemistry, an acyl chloride (or acid chloride) is an organic compound with the functional group −C(=O)Cl. Their formula is usually written R−COCl, where R is a side chain. They are reactive derivatives of carboxylic acids (R−C(=O)OH). A specific example of an acyl chloride is acetyl chloride, CH 3 COCl.

  4. Water softening - Wikipedia

    en.wikipedia.org/wiki/Water_softening

    Water softening is the removal of calcium, magnesium, and certain other metal cations in hard water. The resulting soft water requires less soap for the same cleaning effort, as soap is not wasted bonding with calcium ions.

  5. Ion exchange - Wikipedia

    en.wikipedia.org/wiki/Ion_exchange

    Water softeners are usually regenerated with brine containing 10% sodium chloride. [7] Aside from the soluble chloride salts of divalent cations removed from the softened water, softener regeneration wastewater contains the unused 50–70% of the sodium chloride regeneration flushing brine required to reverse ion-exchange resin equilibria.

  6. Category:Acyl chlorides - Wikipedia

    en.wikipedia.org/wiki/Category:Acyl_chlorides

    Pages in category "Acyl chlorides" The following 40 pages are in this category, out of 40 total. This list may not reflect recent changes. ...

  7. Tsuji–Wilkinson decarbonylation reaction - Wikipedia

    en.wikipedia.org/wiki/Tsuji–Wilkinson...

    The Tsuji–Wilkinson decarbonylation reaction is a method for the decarbonylation of aldehydes and some acyl chlorides. The reaction name recognizes Jirō Tsuji, whose team first reported the use of Wilkinson's catalyst (RhCl(PPh 3) 3) for these reactions: RC(O)X + RhCl(PPh 3) 3 → RX + RhCl(CO)(PPh 3) 2 + PPh 3

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