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When ethane is the feedstock, ethylene is the product. Ethylene is separated from the resulting mixture by repeated compression and distillation. [17] In Europe and Asia, ethylene is obtained mainly from cracking naphtha, gasoil and condensates with the coproduction of propylene, C4 olefins and aromatics (pyrolysis gasoline). [29]
The chief use of ethane is the production of ethylene (ethene) by steam cracking. Steam cracking of ethane is fairly selective for ethylene, while the steam cracking of heavier hydrocarbons yields a product mixture poorer in ethylene and richer in heavier alkenes (olefins), such as propene (propylene) and butadiene, and in aromatic hydrocarbons.
The products produced in the reaction depend on the composition of the feed, the hydrocarbon-to-steam ratio, and on the cracking temperature and furnace residence time. Light hydrocarbon feeds such as ethane, LPGs, or light naphtha give mainly lighter alkenes, including ethylene, propylene, and butadiene.
The products produced in the reaction depend on the composition of the feed, the hydrocarbon-to-steam ratio, and on the cracking temperature and furnace residence time. Light hydrocarbon feeds such as ethane, LPGs or light naphtha give product streams rich in the lighter alkenes, including ethylene, propylene, and butadiene.
The equation of bromination of ethylene to form ethane is: H 2 C=CH 2 + Br 2 →H 2 CBr−CH 2 Br. Unlike hydrogenation, these halogenation reactions do not require catalysts. The reaction occurs in two steps, with a halonium ion as an intermediate. Structure of a bromonium ion. Bromine test is used to test the saturation of hydrocarbons. [17]
Reaction of ethylene oxide with sulfur dioxide in the presence of caesium salts leads to the formation of an 11-membered ... ethane, ethyl, methane ...
The reaction is exothermic (∆H = -280 kJ/mol) and occurs at high temperatures (750–950 ˚C). [3] In the reaction, methane (CH 4) is activated heterogeneously on the catalyst surface, forming methyl free radicals, which then couple in the gas phase to form ethane (C 2 H 6). The ethane subsequently undergoes dehydrogenation to form ethylene ...
1,2-Diiodoethane can be prepared by the reaction of ethylene with iodine (I 2): [2] C 2 H 4 + I 2 ⇌ C 2 H 4 I 2. 1,2-Diiodoethane is most commonly used in organic synthesis in the preparation of samarium(II) iodide or ytterbium(II) iodide in an inert solvent such as THF. [3] Sm + ICH 2 CH 2 I → SmI 2 + H 2 C=CH 2