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  2. Conversion (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Conversion_(chemistry)

    Conversion and its related terms yield and selectivity are important terms in chemical reaction engineering.They are described as ratios of how much of a reactant has reacted (X — conversion, normally between zero and one), how much of a desired product was formed (Y — yield, normally also between zero and one) and how much desired product was formed in ratio to the undesired product(s) (S ...

  3. 1,2,3,4,5-Pentakis (4-butylphenyl)-1,3-cyclopentadiene ...

    en.wikipedia.org/wiki/1,2,3,4,5-Pentakis(4-butyl...

    1,2,3,4,5-Pentakis(4-butylphenyl)-1,3-cyclopentadiene is an organochemical compound from the diene group and a cyclopentadiene derivative. The anion of this compound is used as a sterically demanding ligand, often abbreviated as Cp [BIG] , in the organometallic chemistry of sandwich compounds .

  4. Cyclopentadiene - Wikipedia

    en.wikipedia.org/wiki/Cyclopentadiene

    Cyclopentadiene is a highly reactive diene in the Diels–Alder reaction because minimal distortion of the diene is required to achieve the envelope geometry of the transition state compared to other dienes. [11] Famously, cyclopentadiene dimerizes. The conversion occurs in hours at room temperature, but the monomer can be stored for days at ...

  5. Sandmeyer reaction - Wikipedia

    en.wikipedia.org/wiki/Sandmeyer_reaction

    The Sandmeyer reaction provides a method through which one can perform unique transformations on benzene, such as halogenation, cyanation, trifluoromethylation, and hydroxylation. The reaction was discovered in 1884 by Swiss chemist Traugott Sandmeyer , when he attempted to synthesize phenylacetylene from benzenediazonium chloride and copper(I ...

  6. Fluid catalytic cracking - Wikipedia

    en.wikipedia.org/wiki/Fluid_catalytic_cracking

    A typical fluid catalytic cracking unit in a petroleum refinery. Fluid catalytic cracking (FCC) is the conversion process used in petroleum refineries to convert the high-boiling point, high-molecular weight hydrocarbon fractions of petroleum (crude oils) into gasoline, alkene gases, and other petroleum products.

  7. Linear alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Linear_alkylbenzene

    Linear alkylbenzenes (sometimes also known as LABs) are a family of organic compounds with the formula C 6 H 5 C n H 2n+1.Typically, n lies between 10 and 16, although generally supplied as a tighter cut, such as C 12-C 15, C 12-C 13 and C 10-C 13, for detergent use. [1]

  8. Cracking (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Cracking_(chemistry)

    CH 3 CH 3 → 2 CH 3 ⋅. Because C−C bond energy is so high (377 kJ/mol), [18] this reaction is not observed under laboratory conditions. More common examples of cracking reactions involve retro-Diels–Alder reactions. Illustrative is the thermal cracking of dicyclopentadiene to produce cyclopentadiene.

  9. Chain-growth polymerization - Wikipedia

    en.wikipedia.org/wiki/Chain-growth_polymerization

    Chain initiation is the initial generation of a chain carrier, which is an intermediate such as a radical or an ion which can continue the reaction by chain propagation. Initiation steps are classified according to the way that energy is provided: thermal initiation, high energy initiation, and chemical initiation, etc. Thermal initiation uses ...

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