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C 5 H 12 + 8 O 2 → 5 CO 2 + 6 H 2 O + heat/energy. Like other alkanes, pentanes undergo free radical chlorination: C 5 H 12 + Cl 2 → C 5 H 11 Cl + HCl. Without zeolite catalysts, such reactions are unselective, so with n-pentane, the result is a mixture of the 1-, 2-, and 3-chloropentanes, as well as more highly chlorinated derivatives.
C 5 H 12 FO 2 P: propyl ethylphosphonofluoridate: 2992-95-2 C 5 H 12 NO 3 PS 2: dimethoate: 60-51-5 C 5 H 12 NO 4 PS: omethoate: 1113-02-6 C 5 H 12 N 2: butylmethyldiazene: 4426-46-4 C 5 H 12 N 2: homopiperazine: 505-66-8 C 5 H 12 N 2 O: valeric acid hydrazide: 38291-82-6 C 5 H 12 N 3 OP: tetramethylphosphorodiamidic cyanide: 14445-60-4 C 5 H ...
Cl 2 + H 2 → 2 HCl. As the reaction is exothermic, the installation is called an HCl oven or HCl burner. The resulting hydrogen chloride gas is absorbed in deionized water, resulting in chemically pure hydrochloric acid. This reaction can give a very pure product, e.g. for use in the food industry. The reaction can also be triggered by blue ...
C 5 H 6 N 2 O 2: thymine: 65-71-4 C 5 H 6 O: cyclopentenone: C 5 H 6 O 5: α-Ketoglutaric acid: 328-50-7 C 5 H 7 N 3: 3,4-diaminopyridine: 54-96-6 C 5 H 8 O 2: gamma-Valerolactone: C 5 H 9 NO 3-Dimethylaminoacrolein: 927-63-9 C 5 H 9 NO 2: allylglycine: C 5 H 9 NO 2: proline Pro: 147-85-3 C 5 H 9 NO 4: glutamic acid Glu: 56-86-0 C 5 H 10 ...
The molecular formula C 5 H 12 (molar mass: 72.15 g/mol, exact mass: 72.0939 u) may refer to: Pentanes. Pentane; Eupione, or eupion; Isopentane, or methylbutane;
The original synthesis by Wilkinson and Birmingham, using sodium cyclopentadienide, [4] is still commonly used: [5] 2 NaC 5 H 5 + TiCl 4 → (C 5 H 5) 2 TiCl 2 + 2 NaCl. It can also be prepared by using freshly distilled cyclopentadiene rather than its sodium derivative: [6] 2 C 5 H 6 + TiCl 4 → (C 5 H 5) 2 TiCl 2 + 2 HCl
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[12] [13] Cyclopentane requires safety precautions to prevent leakage and ignition as it is both highly flammable and can also cause respiratory arrest when inhaled. [14] Cyclopentane can be fluorinated to give compounds ranging from C 5 H 9 F to perfluorocyclopentane C 5 F 10. Such species are conceivable refrigerants and specialty solvents ...