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  2. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cistrans_isomerism

    These differences can be very small, as in the case of the boiling point of straight-chain alkenes, such as pent-2-ene, which is 37 °C in the cis isomer and 36 °C in the trans isomer. [5] The differences between cis and trans isomers can be larger if polar bonds are present, as in the 1,2-dichloroethenes .

  3. Pentene - Wikipedia

    en.wikipedia.org/wiki/Pentene

    2-Pentene has two geometric isomers: cis-2-pentene and trans-2-pentene. Cis-2-Pentene is used in olefin metathesis. Branched-chain isomers The ...

  4. C5H10 - Wikipedia

    en.wikipedia.org/wiki/C5H10

    Isomers with the molecular formula C 5 H 10 with CAS numbers. C 5 H 10 is the molecular formula of 13 hydrocarbon isomers (represented by their CAS numbers on the chart). They can be divided into cycloalkanes and alkenes.

  5. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    For monoalkenes, the configuration is often indicated by the prefixes cis- (from Latin "on this side of") or trans- ("across", "on the other side of") before the name, respectively; as in cis-2-pentene or trans-2-butene. The difference between cis-and trans-isomers. More generally, cistrans isomerism will exist if each of the two carbons of ...

  6. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    Traditionally, double bond stereochemistry was described as either cis (Latin, on this side) or trans (Latin, across), in reference to the relative position of substituents on either side of a double bond. A simple example of cistrans isomerism is the 1,2-disubstituted ethenes, like the dichloroethene (C 2 H 2 Cl 2) isomers shown below. [7]

  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 cistrans isomer notation (which only describes relative stereochemistry) that can be used to describe double bonds having two, three or four substituents.

  8. Pentadiene - Wikipedia

    en.wikipedia.org/wiki/Pentadiene

    2,3-pentadiene, H 3 C−CH=C=CH−CH 3, with two enantiomers (R and S). [ 5 ] Well known derivatives containing pentadiene groups include hexadienes , cyclopentadiene , and especially three fatty acids linoleic acid , α- linolenic acid , and arachidonic acid as well as their triglycerides (fats).

  9. C6H12 - Wikipedia

    en.wikipedia.org/wiki/C6H12

    The molecular formula C 6 H 12 may refer to following structural isomers: Acyclic Compounds ... 4-Methyl-2-pentene; ... cis-trans isomers and enantiomers are not ...