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The acid is prepared by the reaction of chlorosulfuric acid with hydrogen peroxide: [3] 2 ClSO 3 H + H 2 O 2 → H 2 S 2 O 8 + 2 HCl. Another method is the electrolysis of moderately concentrated sulfuric acid (60-70%) with platinum electrodes at high current density and voltage: H 2 SO 4 + H 2 O → H 3 O + + HSO 4 − (dissociation of ...
In organic chemistry, organic peroxides are organic compounds containing the peroxide functional group (R−O−O−R′). If the R′ is hydrogen, the compounds are called hydroperoxides, which are discussed in that article. The O−O bond of peroxides easily breaks, producing free radicals of the form RO • (the dot represents an unpaired ...
Hydrogen peroxide is a chemical compound with the formula H 2 O 2.In its pure form, it is a very pale blue [5] liquid that is slightly more viscous than water.It is used as an oxidizer, bleaching agent, and antiseptic, usually as a dilute solution (3%–6% by weight) in water for consumer use and in higher concentrations for industrial use.
2 cro(o 2) 2 + 7 h 2 o 2 + 6 h + → 2 cr 3+ + 10 h 2 o + 7 o 2 Stable adducts of the type CrO(O 2 ) 2 L include those with L = diethyl ether , 1-butanol , ethyl acetate , or amyl acetate . They form by adding a layer of the organic solvent above the chromate/dichromate solution and shaking during the addition of hydrogen peroxide.
This hydrogen peroxide then releases hydrogen peroxide: [(HO) 3 B(OOH)] − + H 2 O ⇌ B(OH) − 4 + H 2 O 2. Several metal hydroperoxide complexes have been characterized by X-ray crystallography. Some form by the reaction of metal hydrides with oxygen gas: [17] L n M−H + O 2 → L n M−O−O−H (L n refers to other ligands bound to the ...
Chemist Linus Pauling first developed the hybridisation theory in 1931 to explain the structure of simple molecules such as methane (CH 4) using atomic orbitals. [2] Pauling pointed out that a carbon atom forms four bonds by using one s and three p orbitals, so that "it might be inferred" that a carbon atom would form three bonds at right angles (using p orbitals) and a fourth weaker bond ...
Anhydrous carboxylic acids form dimers by hydrogen bonding of the acidic hydrogen and the carbonyl oxygen. For example, acetic acid forms a dimer in the gas phase, where the monomer units are held together by hydrogen bonds. [3] Many OH-containing molecules form dimers, e.g. the water dimer.
The bond length is 149 pm, which is larger than in the ground state (triplet oxygen) of the oxygen molecule (3 O 2, 121 pm). This translates into the smaller force constant of the bond (2.8 N/cm vs. 11.4 N/cm for 3 O 2) and the lower frequency of the molecular vibration (770 cm −1 vs. 1555 cm −1 for 3 O 2). [2]