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  2. Sodium peroxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_peroxide

    Sodium peroxide is an inorganic compound with the formula Na 2 O 2.This yellowish solid is the product of sodium ignited in excess oxygen. [3] It is a strong base. This metal peroxide exists in several hydrates and peroxyhydrates including Na 2 O 2 ·2H 2 O 2 ·4H 2 O, Na 2 O 2 ·2H 2 O, Na 2 O 2 ·2H 2 O 2, and Na 2 O 2 ·8H 2 O. [4] The octahydrate, which is simple to prepare, is white, in ...

  3. Peroxide fusion - Wikipedia

    en.wikipedia.org/wiki/Peroxide_fusion

    Sodium peroxide (Na 2 O 2) is used to oxidize the sample that becomes soluble in a diluted acid solution. This method allows complete dissolution of numerous refractory compounds like chromite , magnetite , ilmenite , rutile , and even silicon , carbides , alloys , noble metals and materials with high sulfide contents.

  4. Hydrolysis - Wikipedia

    en.wikipedia.org/wiki/Hydrolysis

    Perhaps the oldest commercially practiced example of ester hydrolysis is saponification (formation of soap). It is the hydrolysis of a triglyceride (fat) with an aqueous base such as sodium hydroxide (NaOH). During the process, glycerol is formed, and the fatty acids react with the base, converting them to salts. These salts are called soaps ...

  5. Metal peroxide - Wikipedia

    en.wikipedia.org/wiki/Metal_peroxide

    Sodium or lithium peroxides are preferred in space applications because of their lower molar mass and therefore higher oxygen yield per unit weight. [3] 2 Na 2 O 2 + 2 CO 2 → 2 Na 2 CO 3 + O 2. Alkali metal peroxides can be used for the synthesis of organic peroxides. One example is the conversion of benzoyl chloride with sodium peroxide to ...

  6. Organic peroxides - Wikipedia

    en.wikipedia.org/wiki/Organic_peroxides

    Diacyl peroxides are typically prepared by treating hydrogen peroxide with acid chlorides or acid anhydrides in the presence of base: [1] H 2 O 2 + 2 RCOCl → (RCO 2) 2 + 2 HCl H 2 O 2 + (RCO) 2 O → (RCO 2) 2 + H 2 O. The reaction competes with hydrolysis of the acylating agent but the hydroperoxide anion is a superior nucleophile relative ...

  7. Dephosphorylation - Wikipedia

    en.wikipedia.org/wiki/Dephosphorylation

    In biochemistry, dephosphorylation is the removal of a phosphate (PO 3− 4) group from an organic compound by hydrolysis. It is a reversible post-translational modification . Dephosphorylation and its counterpart, phosphorylation , activate and deactivate enzymes by detaching or attaching phosphoric esters and anhydrides .

  8. Peroxide - Wikipedia

    en.wikipedia.org/wiki/Peroxide

    In addition to hydrogen peroxide, some other major classes of peroxides are: Peroxy acids, the peroxy derivatives of many familiar acids, examples being peroxymonosulfuric acid and peracetic acid, and their salts, one example of which is potassium peroxydisulfate. Main group peroxides, compounds with the linkage E−O−O−E (E = main group ...

  9. Water splitting - Wikipedia

    en.wikipedia.org/wiki/Water_splitting

    For example, at 2,200 °C (2,470 K; 3,990 °F) about three percent of all H 2 O are dissociated into various combinations of hydrogen and oxygen atoms, mostly H, H 2, O, O 2, and OH. Other reaction products like H 2 O 2 or HO 2 remain minor. At the very high temperature of 3,000 °C (3,270 K; 5,430 °F) more than half of the water molecules are ...