Industrial preparation ethylene

Alkenyl halides such as vinyl chloride (H2C=CHC1) do not form carbocations on treatment with aluminum chloride and so cannot be used m Friedel-Crafts reactions Thus the industrial preparation of styrene from benzene and ethylene does not involve vinyl chloride but proceeds by way of ethylbenzene... 

Not so for synthesis in the chemical industry where a compound must be prepared not only on a large scale but at low cost There is a pronounced bias toward reactants and reagents that are both abundant and inexpensive The oxidizing agent of choice for example in the chemical industry is O2 and extensive research has been devoted to develop mg catalysts for preparing various compounds by air oxidation of readily available starting materials To illustrate air and ethylene are the reactants for the industrial preparation of both acetaldehyde and ethylene oxide Which of the two products is ob tamed depends on the catalyst employed... 

Key intermediates in the industrial preparation of both nicotinamide and nicotinic acid are alkyl pyridines (Fig. 1). 2-Meth5l-5-ethylpyridine (6) is prepared in ahquid-phase process from acetaldehyde. Also, a synthesis starting from ethylene has been reported. Alternatively, 3-methylpyridine (7) can be used as starting material for the synthesis of nicotinamide and nicotinic acid and it is derived industrially from acetaldehyde, formaldehyde (qv), and ammonia. Pyridine is the principal product from this route and 3-methylpyridine is obtained as a by-product. Despite this and largely due to the large amount of pyridine produced by this technology, the majority of the 3-methylpyridine feedstock is prepared in this fashion. 

Dehydrogenation (Section 5.1) Elimination in which H2 is lost from adjacent atoms. The term is most commonly encountered in the industrial preparation of ethylene from ethane, propene from propane, 1,3-butadiene from butane, and styrene from ethylbenzene. 

Only a few of the major developments can be traced here, yet these should give a fair idea of the magnitude and importance of the aliphatic petrochemical growth. It is well to remember that some of the chemistry involved in this industry is old. Four Dutch chemists, otherwise unrecalled today, prepared ethylene dichloride by addition of chlorine to ethylene in 1795, and the synthesis of ethyl alcohol from ethylene via sulfuric acid absorption was studied by Berthelot in 1855 (8). Of course, this was coal-gas ethylene, and the commercial application of this synthesis did not occur until 75 years later, in 1929, when ethylene produced from natural gas was first converted into ethyl alcohol on a practical scale (84). 

Natural gas liquids represent a significant source of feedstocks for the production of important chemical building blocks that form the basis for many commercial and industrial products. Ethylene (qv) is produced by steam-cracking the ethane and propane fractions obtained from natural gas, and the butane fraction can be catalytically dehydrogenated to yield 1,3-butadiene, a compound used in the preparation of many polymers (see Butadiene). The -butane fraction can also be used as a feedstock in the manufacture of MTBE. 

Vinyl chloride (H2C=CHC1), the starting material used in the industrial preparation of poly(vinyl chloride), is prepared by a two-step process that begins with the reaction of Cl2 with ethylene to yield 1,2-dichloroethane ... 

Many simple alcohols are important raw materials in the industrial synthesis of polymers, fibers, explosives, plastics, and pharmaceutical products. Phenols are widely used in the preparation of plastics and dyes. Solutions of phenols are used as antiseptics and disinfectants. Some uses of polyhydric alcohols depend on their relatively high boiling points. For instance, glycerine is used as a wetting agent in cosmetic preparations. Ethylene glycol (bp 197°C), which is miscible with water, is used in commercial permanent antifreeze. 

Thus, the industrial preparation of styrene from benzene and ethylene does not involve vinyl chloride but proceeds by way of ethylbenzene. 

Ethanediol. See Ethylene glycol Ethanoic acid. See Acetic acid Ethanol, 128, 130, 580-581 acidity of, 135, 740-741 and benzaldehyde, acetal from, 669 biological oxidation of, 600—602 chemical shifts, 606 conversion to diethyl ether, 592 dehydration of, 182 dipole moment of, 130, 863 by fermentation, 580-581 hydrogen bonding in, 130-131 industrial preparation of, 223, 581 physical properties of, 130, 132-133, 580 reduction of aryl diazonium salts by, 894, 907... 

A third example is the industrial preparation of ethylene glycol (HOCH2CH2OH) by hydrolysis of ethylene oxide in dilute sulfuric acid. This reaction and its mechanism (Mechanism 16.3) illustrate the difference between the ring openings of ethylene oxide discussed in the preceding section and the acid-catalyzed ones described here. In acid, the species that is attacked by the nucleophile is not the epoxide itself, but rather its... 

Ethylene [74-85-1] is the monomer used to make LDPE [9002-88-4]. The predominant method of manufacture of ethylene is high temperature cracking of natural gas or crude oil. Some properties of ethylene are collected in Table 1. The principal method for the industrial preparation of ethylene is thermal cracking of hydrocarbons. Small amounts of comonomers, such as vinyl acetate [108-05-4], methyl acrylate [96-33-3], or ethyl aciylate [108-88-5], can be added to modify... 

Alkenes are also important precursors in the chemical industry. The two most important industrial alkenes, ethylene and propylene, are formed from cracking petroleum, and are used as starting materials for preparing a wide variety of compounds (Figure 8.2) ... 

This reaction is used industrially to prepare ethylene while simultaneously serving as a source of hydrogen gas. Explain why dehydrogenation only works at high temperatures. 

---