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The main use of ozonolysis is for the conversion of unsaturated fatty acids to value-added derivatives. Ozonolysis of oleic acid is an important route to azelaic acid. The coproduct is nonanoic acid: [20] CH 3 (CH 2) 7 CH=CH(CH 2) 7 CO 2 H} + 4 O 3 → HO 2 C(CH 2) 7 CO 2 H} + CH 3 (CH 2) 7 CO 2 H
Methylpentene is an alkene with a molecular formula C 6 H 12.The prefix "methyl-" is derived from the fact that there is a methyl(CH 3) branch, the word root "-pent-" is derived from the fact that there are 5 carbon atoms in the parent chain, while the "-ene" suffix denotes that there is a double bond present, as per IUPAC nomenclature. [1]
Solubility in water. 2.26 wt % (20 °C) Refractive index (n D) 1.4012 (20 °C) Hazards GHS labelling: [1] ... 3-Methyl-2-pentanone (methyl sec-butyl ketone) ...
Pentenes are alkenes with the chemical formula C 5 H 10.Each molecule contains one double bond within its molecular structure. Six different compounds are in this class, differing from each other by whether the carbon atoms are attached linearly or in a branched structure and whether the double bond has a cis or trans form.
The oxime first reacts with the ozone to form the corresponding carbonyl oxide, undergoes 1,3-dipolar cycloaddition with the carbonyl reactant to form the cyclic ozonide, as usual for the Criegee intermediate in the ozonolysis of alkenes. If no carbonyl compound is used, the carbonyl oxide may dimerize and form 1,2,4,5-tetraoxanes.
1 mole of O 2 → 2 moles of MnO(OH) 2 → 2 mole of I 2 → 4 mole of S 2 O 2− 3. Therefore, after determining the number of moles of iodine produced, we can work out the number of moles of oxygen molecules present in the original water sample. The oxygen content is usually presented in milligrams per liter (mg/L).
Fe 3+ + H 2 O 2 → Fe 2+ + HOO· + H + (regeneration of Fe 2+ catalyst) H 2 O 2 → HO· + HOO· + H 2 O (Self scavenging and decomposition of H 2 O 2) the reaction steps presented here are just a part of the reaction sequence, see reference for more details. Photocatalytic oxidation with TiO 2: [15] TiO 2 + UV → e − + h + (irradiation of ...
3-Methyl-3-penten-2-one is an unsaturated aliphatic ketone. It is an isomer of mesityl oxide and isomesityl oxide. It is a precursor of 3-methyl-2-pentanone (methyl sec-butyl ketone) and is obtained by acid-catalyzed dehydration of 4-hydroxy-3-methyl-2-pentanone. It is used as an intermediate in organic chemistry syntheses. [1]