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Cyclopentane (also called C pentane) [4] is a highly flammable alicyclic hydrocarbon with chemical formula C 5 H 10 and CAS number 287-92-3, consisting of a ring of five carbon atoms each bonded with two hydrogen atoms above and below the plane. It is a colorless liquid with a petrol-like odor. Its freezing point is −94 °C and its boiling ...
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.
2 C 5 H 6 + TiCl 4 → (C 5 H 5) 2 TiCl 2 + 2 HCl. Focusing on the geometry of the Ti center, Cp 2 TiCl 2 adopts a distorted tetrahedral geometry (counting Cp as a monodentate ligand). The Ti-Cl distance is 2.37 Å and the Cl-Ti-Cl angle is 95°. [7]
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: cyclopentane: 287-92-3 C 5 H 10 N 2 O 3: glutamine Gln: 56-85-9 C 5 H 10 O 2: pivalic acid: C 5 H 10 O 2: valeric acid: C 5 H 10 O 2: 3-Methylbutanoic acid: C 5 H 10 O 4: deoxyribose: 533-67-5 C 5 H 11 NO 2: valine Val: 660-88-8 C ...
Arenes, such as C 6 (CH 3) 6 react to give the piano-stool complexes [Ti(C 6 R 6)Cl 3] + (R = H, CH 3; see figure above). This reaction illustrates the high Lewis acidity of the TiCl + 3 entity, which is generated by abstraction of chloride from TiCl 4 by AlCl 3. [12]
C 5 H 9 Cl 2 N 3 O 2: Molar mass: 214.05 g·mol −1 Appearance Orange crystals Odor: Odourless Melting point: 30 °C (86 °F; 303 K) log P: 1.375 Acidity (pK a) 10.194 Basicity (pK b) 3.803 Pharmacology
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Upon contact, H 2 O and HCl combine to form hydronium cations [H 3 O] + and chloride anions Cl − through a reversible chemical reaction: HCl + H 2 O → [H 3 O] + + Cl −. The resulting solution is called hydrochloric acid and is a strong acid.