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  2. 1,3-Dichloropropene - Wikipedia

    en.wikipedia.org/wiki/1,3-Dichloropropene

    1,3-Dichloropropene, sold under diverse trade names, is an organochlorine compound with the formula C 3 H 4 Cl 2. It is a colorless liquid with a sweet smell. It is a colorless liquid with a sweet smell.

  3. File:Cis-1,3-Dichloropropene-3D-balls.png - Wikipedia

    en.wikipedia.org/wiki/File:Cis-1,3...

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  4. File:Cis-1,3-Dichloropropene.svg - Wikipedia

    en.wikipedia.org/wiki/File:Cis-1,3...

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  5. 1,3-Dichloropropane - Wikipedia

    en.wikipedia.org/wiki/1,3-Dichloropropane

    1,3-Dichloropropane is a compound of chlorine, hydrogen, and carbon. It may be found as a contaminant in soil fumigants containing 1,3-dichloropropene . [ 2 ] It has low acute toxicity.

  6. Kurnakov test - Wikipedia

    en.wikipedia.org/wiki/Kurnakov_test

    The Kurnakov test, also known as Kurnakov's reaction, is a chemical test that distinguishes pairs of cis- and trans-isomers of [PtA 2 X 2] (A = NH 3, X = halogen or pseudohalide). Upon treatment with thiourea , the trans -dihalides give less soluble white products, whereas the cis -dihalides give more soluble yellow products.

  7. 1,2-Dichloroethylene - Wikipedia

    en.wikipedia.org/wiki/1,2-dichloroethylene

    1,2-Dichloroethylene or 1,2-DCE is the name for a pair of organochlorine compounds with the molecular formula C 2 H 2 Cl 2. The two compounds are isomers, each being colorless liquids with a sweet odor. It can exist as either of two geometric isomers, cis-1,2-dichloroethene or trans-1,2-dichloroethene, but is often used as a mixture of the two ...

  8. (1R,3R)-1,2,3-Trimethylcyclopentane - Wikipedia

    en.wikipedia.org/wiki/(1R,3R)-1,2,3-trimethylcyc...

    Because (1R,3R)-1,2,3-trimethylcyclopentane is a cycloalkane, its three methyl substituents are capable of exhibiting cis/trans isomerism. This implies that the methyl groups in positions 1,2, and 3 may occupy different spatial arrangements (i.e.they may either lay cis or trans with respect to each other).

  9. Cycloheptene - Wikipedia

    en.wikipedia.org/wiki/Cycloheptene

    With cycloheptene, the cis-isomer is always assumed but the trans-isomer does also exist. One procedure for the organic synthesis of trans-cycloheptene is by singlet photosensitization of cis-cycloheptene with methyl benzoate and ultraviolet light at −35 °C. [2] The double bond in the trans isomer is very strained. [3]