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  2. Cracking (chemistry) - Wikipedia

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

    The rate of cracking and the end products are strongly dependent on the temperature and presence of catalysts. Cracking is the breakdown of large hydrocarbons into smaller, more useful alkanes and alkenes. Simply put, hydrocarbon cracking is the process of breaking long-chain hydrocarbons into short ones. This process requires high temperatures ...

  3. Steam cracking - Wikipedia

    en.wikipedia.org/wiki/Steam_cracking

    Steam cracking is a petrochemical process in which saturated hydrocarbons are broken down into smaller, often unsaturated, hydrocarbons. It is the principal industrial method for producing the lighter alkenes (or commonly olefins ), including ethene (or ethylene ) and propene (or propylene ).

  4. Dehydrogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrogenation

    The cracking processes especially fluid catalytic cracking and steam cracker produce high-purity mono-olefins from paraffins. Typical operating conditions use chromium (III) oxide catalyst at 500 °C. Target products are propylene, butenes, and isopentane, etc. These simple compounds are important raw materials for the synthesis of polymers and ...

  5. Fluid catalytic cracking - Wikipedia

    en.wikipedia.org/wiki/Fluid_catalytic_cracking

    As also depicted in Figure 2, the cycloalkanes (naphthenes) formed by the initial breakup of the large molecules are further converted to aromatics such as benzene, toluene, and xylenes, which boil in the gasoline boiling range and have much higher octane ratings than alkanes. In the cracking process carbon is also produced which gets deposited ...

  6. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    The compound with the formula (C 5 H 5) 2 Fe 2 (CO) 4 exists as three isomers in solution. In one isomer the CO ligands are terminal. When a pair of CO are bridging, cis and trans isomers are possible depending on the location of the C 5 H 5 groups. [7] Another example in organometallic chemistry is the linkage isomerization of ...

  7. Dehydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrohalogenation

    CH 2 Cl-CH 2 Cl → CH 2 =CHCl + HCl. The resulting HCl can be reused in oxychlorination reaction. Thermally induced dehydrofluorinations are employed in the production of fluoroolefins and hydrofluoroolefins. One example is the preparation of 1,2,3,3,3-pentafluoropropene from 1,1,2,3,3,3-hexafluoropropane: CF 2 HCH(F)CF 3 → CHF=C(F)CF 3 + HF

  8. Polymerization - Wikipedia

    en.wikipedia.org/wiki/Polymerization

    [1] [2] [3] There are many forms of polymerization [4] and different systems exist to categorize them. IUPAC definition for polymerization In chemical compounds , polymerization can occur via a variety of reaction mechanisms that vary in complexity due to the functional groups present in the reactants [ 3 ] and their inherent steric effects .

  9. Alkanolamine - Wikipedia

    en.wikipedia.org/wiki/Alkanolamine

    2-Aminoalcohols are an important class of organic compounds that are often generated by the reaction of amines with epoxides: C 2 H 4 O + R−NH 2 → RNHC 2 H 4 OH. Simple alkanolamines are used as solvents, synthetic intermediates, and high-boiling bases. [1] Hydrogenation or hydride reduction of amino acids gives the