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  2. File:Trans-2-hexene.svg - Wikipedia

    en.wikipedia.org/wiki/File:Trans-2-hexene.svg

    This file contains additional information, probably added from the digital camera or scanner used to create or digitize it. If the file has been modified from its original state, some details may not fully reflect the modified file.

  3. trans-2-Hexenal - Wikipedia

    en.wikipedia.org/wiki/Trans-2-hexenal

    trans-2-Hexenal is an organic unsaturated aldehyde with a six-carbon chain. This clear, pale yellow liquid has a green, leafy, herbal fruit smell. It occurs naturally in a wide variety of plants, fruits, vegetables, and spices, and appears to be an important mediating and signalling chemical in plant-fungus and plant-insect interactions, such as the symbiosis between acacia ants and Acacias.

  4. 2-Hexyne - Wikipedia

    en.wikipedia.org/wiki/2-Hexyne

    2-Hexyne can be semihydrogenated to yield 2-hexene or fully hydrogenated to hexane. [3] With appropriate noble metal catalysts it can selectively form cis-2-hexene. [4] 2-Hexyne can act as a ligand on gold atoms. [5] With strong sulfuric acid, the ketone 2-hexanone is produced. However this reaction also causes polymerization and charring. [6]

  5. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    Because the cis–trans and E–Z systems compare different groups on the alkene, it is not strictly true that Z corresponds to cis and E corresponds to trans. For example, trans-2-chlorobut-2-ene (the two methyl groups, C1 and C4, on the but-2-ene backbone are trans to each other) is (Z)-2-chlorobut-2-ene (the chlorine and C4 are together ...

  6. Hexyne - Wikipedia

    en.wikipedia.org/wiki/Hexyne

    The hexynes are a subgroup from the group of alkynes.It consists of several isomeric compounds having the formula C 6 H 10.. The linear and branched members are: 1-Hexyne (n-butylacetylene)

  7. E–Z notation - Wikipedia

    en.wikipedia.org/wiki/E–Z_notation

    E–Z configuration, or the E–Z convention, is the IUPAC preferred method of describing the absolute stereochemistry of double bonds in organic chemistry.It is an extension of cis–trans isomer notation (which only describes relative stereochemistry) that can be used to describe double bonds having two, three or four substituents.

  8. The 2025 Oscars worst-dressed list: 12 looks that missed the ...

    www.aol.com/news/2025-oscars-worst-dressed-list...

    The 2025 Academy Awards were held in Los Angeles on Sunday night. Though there were many well-dressed stars, a few others missed the mark. Elle Fanning's gown was underwhelming, and Joe Locke wore ...

  9. Hexene - Wikipedia

    en.wikipedia.org/wiki/Hexene

    In organic chemistry, hexene is a hydrocarbon with the chemical formula C 6 H 12. The prefix "hex" is derived from the fact that there are 6 carbon atoms in the molecule, while the " -ene " suffix denotes that there is an alkene present—two carbon atoms are connected via a double bond .

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