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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.
[Ti 2 Cl 9] −: white/colourless d 0 d 0: face-sharing bioctahedron Ti-Cl(terminal) = 2.23 Å, 2.45 (terminal) (N(PCl 3) 2) + salt) [4] [Ti 2 Cl 9] 3-orange (t 2g) 1 (t 2g) 1: face-sharing bioctahedron Ti-Ti =3.22 Å Ti-C1(terminal) = 2.32-2.35 Å, Ti-Cl(bridge) = 2.42-2.55 Å ((NEt 4 +) 3) 3 salt) [5] [Ti 2 Cl 10] 2−: colourless d 0 d 0 ...
C 9 H 2 Cl 6 O 3: chlorendic anhydride: 115-27-5 C 9 H 4 Cl 3 NO 2 S: folpet: 133-07-3 C 9 H 4 Cl 8 O: isobenzan: 297-78-9 C 9 H 4 O 5: trimellitic anhydride: 552-30-7 C 9 H 5 BrCrO 3: bromobenzenechromium tricarbonyl: 12082-02-9 C 9 H 5 CrFO 3: fluorobenzenechromium tricarbonyl: 12082-05-2 C 9 H 5 CrIO 3: iodobenzenechrornium tricarbonyl ...
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 12 O: isobutyl methyl ether: 625-44-5 C 5 H 12 O 2 ...
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 molecular formula C 5 H 9 ClO (molar mass: 120.58 g/mol) may refer to: Pentanoyl chloride , an acyl chloride derived from pentanoic acid Pivaloyl chloride , a branched-chain acyl chloride
Work in the early 1980s by Basolo found the S N 2 replacement of CO in Rh(η 5-C 9 H 7)(CO) 2 to be 10 8 times faster than in Rh(η 5-C 5 H 5)(CO) 2. Shortly afterwards, Basolo tested the effect of the indene ligand on Mn(η 5 -C 9 H 7 )(CO) 3 , the cyclopentadienyl analogue of which having been shown to be inert to CO substitution.
[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 ...