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Cyclopentanone is common precursor to fragrances, especially those related to jasmine and jasmone. Examples include 2-pentyl- and 2-heptylcyclopentanone. [4] It is a versatile synthetic intermediate, being a precursor to cyclopentobarbital. [5] Cyclopentobarbital, a drug made from cyclopentanone
2-Cyclopentenones can be synthesized in a number of ways. One of the routes involves elimination of α-bromo-cyclopentanone using lithium carbonate [2] and Claisen condensation-decarboxylation-isomerization cascades of unsaturated diesters as shown below. [3] Industrial synthesis of cyclopentenone
Cyclopentene is a chemical compound with the formula (CH 2) 3 (CH) 2. It is a colorless liquid with a petrol-like odor. It has few applications, and thus is mainly used as a minor component of gasoline, present in concentrations of less than 1%. [1] [2] It is one of the principal cycloalkenes.
The molecular formula C 5 H 8 O (molar mass: 84.12 g/mol) may refer to: Cyclopentanone; 2,3-Dihydropyran; trans-2-Methyl-2-butenal; 2-Methylbut-3-yn-2-ol; 3-Penten-2-one
Structure of xenon oxytetrafluoride, an example of a molecule with the square pyramidal coordination geometry. Square pyramidal geometry describes the shape of certain chemical compounds with the formula ML 5 where L is a ligand. If the ligand atoms were connected, the resulting shape would be that of a pyramid with a square base.
Chemical formula. C 5 H 10 O: Molar mass: 86.1323 g/mol Appearance Colorless liquid Density: 0.949 g/mL Melting point: ... Cyclopentanone: Except where otherwise ...
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.
The seesaw geometry occurs when a molecule has a steric number of 5, with the central atom being bonded to 4 other atoms and 1 lone pair (AX 4 E 1 in AXE notation). An atom bonded to 5 other atoms (and no lone pairs) forms a trigonal bipyramid with two axial and three equatorial positions, but in the seesaw geometry one of the atoms is replaced ...