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  2. Crotyl group - Wikipedia

    en.wikipedia.org/wiki/Crotyl_group

    Crotyl groups attached to R. A crotyl group is an organic functional group with the formula RCH 2 CH=CHCH 3. [1] Systematically, it is called a but-2-en-1-yl group and exhibits geometric isomerism, being either cis (Z) or trans (E).

  3. But-2-ene - Wikipedia

    en.wikipedia.org/wiki/But-2-ene

    But-2-ene is an acyclic alkene with four carbon atoms. It is the simplest alkene exhibiting cis/trans-isomerism (also known as (E/Z)-isomerism); that is, it exists as two geometric isomers cis-but-2-ene ((Z)-but-2-ene) and trans-but-2-ene ((E)-but-2-ene). It is a petrochemical, produced by the catalytic cracking of crude oil or the dimerization ...

  4. File:Trans-2-butene.svg - Wikipedia

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

    This image of a simple structural formula is ineligible for copyright and therefore in the public domain, because it consists entirely of information that is common property and contains no original authorship.

  5. Raffinate - Wikipedia

    en.wikipedia.org/wiki/Raffinate

    In naphtha cracking process, C4R2 refers to C4 residual obtained after separation of 1,3-butadiene and isobutylene from C4 raffinate stream and which mainly consists of cis- or trans-2-butene 50~60 wt%, 1-butene 10~15 wt%, and n-butane ~20 wt%. Normally C4R2 is a side product in tert-butyl alcohol plant if C4R1 is used for feed.

  6. IUPAC nomenclature of organic chemistry - Wikipedia

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

    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. It is IUPAC convention to describe all alkenes using absolute descriptors of Z- (same side) and E- (opposite) with the Cahn–Ingold–Prelog priority rules (see also E–Z notation ).

  7. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    Structural formula nonanoic acid: pelargonic acid 1-octanecarboxylic acid: CH 3 (CH 2) 7 COOH benzene-1,3,5-tricarboxylic acid: trimesic acid: C 6 H 3 (COOH) 3 (E)-3-phenylprop-2-enoic acid: cinnamic acid trans-cinnamic acid phenylacrylic acid cinnamylic acid 3-phenylacrylic acid (E)-cinnamic acid benzenepropenoic acid isocinnamic acid: C 6 H 5 ...

  8. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    Another example of this is the relationship between oleic acid and elaidic acid; oleic acid, the cis isomer, has a melting point of 13.4 °C, making it a liquid at room temperature, while the trans isomer, elaidic acid, has the much higher melting point of 43 °C, due to the straighter trans isomer being able to pack more tightly, and is solid ...

  9. Butene - Wikipedia

    en.wikipedia.org/wiki/Butene

    In the chemical structures above, the small blue numbers in the structure images are the numbering of the atoms in the main backbone chain of the molecules. Other organic compounds have the formula C 4 H 8 , namely cyclobutane and methylcyclopropane , but are not alkenes and do not fall under the name butene .