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  2. Bromocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Bromocyclohexane

    A mixture of cis-decalin and CXB can simultaneously match optical index and density of PMMA. [1] Due to the moderate dielectric constant of CXB (ε = 7.9 [2]), PMMA acquires charges that can be screened by the addition of salt (e.g. tetrabutyl ammonium bromide), leading to a very good approximation of colloidal hard sphere. [3]

  3. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    Multiple double bonds take the form -diene, -triene, etc., with the size prefix of the chain taking an extra "a": CH 2 =CHCH=CH 2 is buta-1,3-diene. Simple cis and trans isomers may be indicated with a prefixed cis-or trans-: cis-but-2-ene, trans-but-2-ene. However, cis-and trans-are relative descriptors.

  4. Cyclododecatriene - Wikipedia

    en.wikipedia.org/wiki/Cyclododecatriene

    Cyclododecatrienes are cyclic trienes with the formula C 12 H 18.Four isomers are known for 1,5,9-cyclododecatriene. The trans,trans,cis-isomer is a precursor in the production of nylon-12.

  5. 2-chloro-4-carboxymethylenebut-2-en-1,4-olide isomerase

    en.wikipedia.org/wiki/2-chloro-4-carboxym...

    The systematic name of this enzyme class is 2-chloro-4-carboxymethylenebut-2-en-1,4-olide cis-trans-isomerase.

  6. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    Very often, cis–trans stereoisomers contain double bonds or ring structures. In both cases the rotation of bonds is restricted or prevented. [4] When the substituent groups are oriented in the same direction, the diastereomer is referred to as cis, whereas when the substituents are oriented in opposing directions, the diastereomer is referred to as trans.

  7. Descriptor (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Descriptor_(Chemistry)

    See: E-Z notation Violet leaf aldehyde, systematic name (E,Z)-nona-2,6-dienal, is a compound having one (E)- and one (Z)-configured double bond. The descriptors (E) (from German entgegen, 'opposite') and (Z) (from German zusammen, 'together') are used to provide a distinct description of the substitution pattern for alkenes, cumulenes or other double bond systems such as oximes.

  8. Enoyl CoA isomerase - Wikipedia

    en.wikipedia.org/wiki/Enoyl_CoA_isomerase

    Enoyl-CoA-(∆) isomerase (EC 5.3.3.8, also known as dodecenoyl-CoA-(∆) isomerase, 3,2-trans-enoyl-CoA isomerase, ∆3(cis),∆2(trans)-enoyl-CoA isomerase, or acetylene-allene isomerase, [1] is an enzyme that catalyzes the conversion of cis- or trans-double bonds of coenzyme A (CoA) bound fatty acids at gamma-carbon (position 3) to trans double bonds at beta-carbon (position 2) as below:

  9. Cycloheptene - Wikipedia

    en.wikipedia.org/wiki/Cycloheptene

    Cycloheptene is a 7-membered cycloalkene with a flash point of −6.7 °C. It is a raw material in organic chemistry and a monomer in polymer synthesis. Cycloheptene can exist as either the cis - or the trans -isomer.