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Chloranil is a quinone with the molecular formula C 6 Cl 4 O 2. Also known as tetrachloro-1,4-benzoquinone, it is a yellow solid. Also known as tetrachloro-1,4-benzoquinone, it is a yellow solid. Like the parent benzoquinone, chloranil is a planar molecule [ 2 ] that functions as a mild oxidant.
Chloranilic acid is an organic compound with the chemical formula C 6 Cl 2 O 2 (OH) 2. It is a red-orange solid. The compound is obtained by hydrolysis of chloranil: C 6 Cl 4 O 2 + 2 H 2 O → C 6 Cl 2 O 2 (OH) 2 + 2 HCl. It is centrosymmetric, planar molecule. It also crystallizes as a dihydrate. [2]
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (or DDQ) is the chemical reagent with formula C 6 Cl 2 (CN) 2 O 2. This oxidant is useful for the dehydrogenation of alcohols, [3] phenols, [4] and steroid ketones. [5] DDQ decomposes in water, but is stable in aqueous mineral acid. [6]
Relative to benzoquinone, more strongly oxidizing quinones include chloranil and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (also known as DDQ). [6] The oxidizing power of quinones is enhanced by the presence of acids. [7] In acidic conditions, quinone undergoes two-electron and two-proton reduction to hydroquinone.
Chlorothalonil (2,4,5,6-tetrachloroisophthalonitrile) is an organic compound mainly used as a broad spectrum, nonsystemic fungicide, with other uses as a wood protectant, pesticide, acaricide, and to control mold, mildew, bacteria, algae. [2]
Natural polyphenols molecular formulas represent a class of natural aromatic organic compounds in which one or more hydroxy groups are attached directly to the benzene ring, generally formed from C, H and O. [1] The entries are sorted by mass.
Mass spectrometry was sufficient to determine the molecular mass of the ion, but it was too small for structure determination from the fragmentation pattern. The ion was found to have the molecular formula ClN 2 O 2 -1 (containing two oxygen atoms, two nitrogen atoms, and one chlorine atom) by electrospray ionisation mass spectrometry .
Results have shown that most particulate Cl-PAH concentration detected in urban air tended to be high in colder seasons and low in warmer seasons. This study also determined through compositional analysis that relatively low molecular weight Cl-PAHs dominated in warmer seasons and high molecular weight Cl-PAHs dominated in colder seasons. [4]