1 2 3 4 5 6 Hexachlorocyclohexane Stereoisomers

Benzene hexachloride bhc any of several stereoisomers of 1 2 3 4 5 6 hexachlorocyclohexane formed by the light induced addition of chlorine to benzene one of these isomers is an insecticide called lindane or gammexane.

1 2 3 4 5 6 hexachlorocyclohexane stereoisomers. 1 four wedges 1 2 3 5 have wedges if you put 5 wedge cl bonds on the ring then imagine flipping the ring over you now have 5 dashed bonds and therefore 1 wedge bond which i already listed in the same way having all 6 cl s up is the same as having them all down. The wedge dash notation for the compound would look like this. Administration of α 1 2 3 4 5 6 hexachlorocy clohexane α hch to rats decreased the utilization of 2 14c orotic acid for the synthesis of liver cytidine nucleotides. Cas number of the unlabelled compound 58 89 9.

How many stereoisomers of 1 2 3 4 5 6 hexachlorocyclohexane possible chemistry hydrocarbons. This structure has nine stereoisomers eight diastereomers one of which has two enantiomers which differ by the stereochemistry of the individual chlorine substituents on the cyclohexane. 99 atom d. Pesticides pesticide metabolites.

Benzene hexachloride was first prepared in 1825. General description α 1 2 3 4 5 6 hexachloroc yclohexane is a racemic compound with anticonvulsant and tremorogenic activities and its accumulation in cerebral white over grey matter in rats was confirmed. In the same order the chlorine atoms will be placed on a dash carbon 1 on a wedge on a dash on a wedge on a dash and finally on a wedge carbon 6. 7 and 8 are same and everything else is correct.

See vitamin vitamin group of organic substances that are required in the diet of humans and animals for normal growth maintenance of life and normal. C 6 cl 6 d 6. Also putting 4 wedges at carbons 1 3 4 5 or 1 2 4 5 is the same as 1 3 or. 1 2 3 4 5 6 hexachloro 1 2 3 4 5 6 13c6 cyclohexane c6h6cl6 cid 71309660 structure chemical names physical and chemical properties classification patents.

Hexachlorocyclohexane hch c 6 h 6 cl 6 is any of several polyhalogenated organic compounds consisting of a six carbon ring with one chlorine and one hydrogen attached to each carbon. All of the stereoisomers of 1 2 3 4 5 6 hexachlorocyclohexane have very similar rates of e2 reaction except the following stereoisomer which reacts about 7000 times more slowly than the others.