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1.3- Butadiene benzene

Methoxy-3-phenylthio-1,3-butadiene Benzene, [(2-methoxy-l-methylene-2-propenyl)thio]- (9) (60603-16-9)... [Pg.107]

For more information on the health effects associated with exposure to specific components of the gasoline mixture, please refer to the ATSDR toxicological profiles on 1,3-butadiene, benzene,... [Pg.17]

In Fig. 4, the relative contribution of individual airborne hazardous pollutants to lung cancer rates are presented. The results presented in Fig. 4 were obtained after removing cancer incidents that are directly attributable to tobacco smoke which primarily is an indoor pollutant. As seen from this figure the PIC (which includes PAH), 1,3-butadiene, benzene, and formaldehyde, which are produced by all combus-tion/incineration processes, were the largest contributors to lung cancer, representing in excess of 50% of the risk, far more than dioxins. However, because different chemicals target different parts of the body. [Pg.1384]

The NPA electron distribution can be related to the VB concept of resonance structures. The orbitals corresponding to localized structures and those representing delocalization can be weighted. For example, Scheme 1.5 shows the relative weighting of the most important resonance structures for 1,3-butadiene, benzene, the benzyl cation, formamide, and the formate anion. These molecules are commonly used examples of the effect of conjugation and resonance on structure and reactivity. [Pg.62]

Elevated levels of toxic hydrocarbons, such as 1,3-butadiene, benzene, toluene and xylenes were found. This study also showed that vehicle exhaust is the major source of VOCs in Mexico City. [Pg.162]

Petroleum feedstock, natural gas and tar represent the main production chain drivers for the petrochemical industry (Bell, 1990). From these, many important petrochemical intermediates are produced, including ethylene, propylene, butylenes, butadiene, benzene, toluene, and xylene. These essential intermediates are then converted to many other intermediates and final petrochemical products, constructing a complex petrochemical network. Figure 1.4 depicts a portion of the petrochemical alternative routes to produce cellulous acetate. [Pg.13]

The FE MO, HMO, and PPP methods are restricted to planar conjugated molecules (e.g., butadiene, benzene, pyridine), and make the pi-electron approximation of treating only those valence electrons that are in pi MOs (those that have eigenvalue — 1 for reflection in the molecular plane) they assume the existence of a pi-electron Hamiltonian Hm of the form... [Pg.290]

For many simple compounds having no more than one double bond, the modern picture may be quite adequately represented by the Lewis structures (although the Lewis rules are noncommittal about the shapes of molecules). For compounds such as butadiene, benzene, and nitrous oxide, where there is extensive delocalization of electron density, the Lewis structures are not as suitable as the x-electron structures or, better still, as the streamer structures. Both of the latter type, however, are more difficult to draw and, for more complex molecules, more difficult to visualize they become extremely unwieldy when one attempts to use them to represent the progress of a chemical reaction. [Pg.54]

Feedstocks for the petrochemical industry are produced mainly from crude oil (Chapter 18) and natural gas (Chapter 20). About 90 percent of all organic chemicals are manufactured from just six feedstocks synthesis gas, ethylene, propylene, butadiene, benzene, and /7-xylene, with synthesis gas accounting for over half of these feedstocks. Although a lot of syngas for the manufacture of ammonia, methanol, and other chemicals is... [Pg.900]

Olefins and aromatics. More than 90 of all today s chemicals go back to ethylene, propone, butadiene, benzene and xylenes. Many academic... [Pg.94]

In a solvent such as methyl tetrahydrofuran (MTHF), anion and cation states of an unsaturated hydrocarbon are typically stabilized by 1-1.5 eV. For example, the ground state anions of butadiene, benzene, naphthalene, and styrene, which are unstable by 1.1 eV or less in the gas phase, are all stable in MTHF glass at 77 K making possible their study by optical spectroscopy. On the other hand, the anions of ethylene and 1,4 cyclohexadiene which are unstable by about 1.8 eV in the gas phase have not been prepared in MTHF glass. Presumably, the use of a more polar solvent would allow the preparation of these anions in a glass. [Pg.3]

CALCULATION OF ENERGIES FOR MOLECULES OF BUTADIENE, BENZENE AND FULVENE... [Pg.439]

The reaction between ethyne and phosgene has also been studied under photochemical conditions (>220 nm) [2185a]. As in the analogous reaction with ethene (see Section 10.1.2), the phosgene merely acts as a convenient source of chlorine radicals the principal products were CO, CHj=CHCl, 1-chloro-l, 3-butadiene, benzene and polymer trace amounts of HC Cl and CgHjCl were also detected [2185a]. [Pg.417]

Ethylene, toluene, propylene, xylenes, butadiene, benzene, chlorine... [Pg.162]

Olefins and Aromatics ethylene, propylene, butadiene, benzene, toluene and xylene ... [Pg.231]

Chlorine with ammonia, acetylene, butadiene, benzene and other petroleum fractions, hydrogen, sodium carbides, turpentine and finely divided powdered metals. [Pg.1]

Figure 3. Selectivities of hydrogen, butadiene, benzene, and polycyclics in the thermal reaction of ethylene... Figure 3. Selectivities of hydrogen, butadiene, benzene, and polycyclics in the thermal reaction of ethylene...
These routes are the sources of the eight building blocks — ammonia, methanol, ethylene, propylene, butadiene, benzene, toluene, and xylene — from which virtually all large tormage petrochemicals are derived. Figure 15.1 represents a simplified version of the production of these chemicals from petroleum and natural gas. Simplified flow diagrams for the production of some polymers from these basic petrochemicals are shown in Figures 15.2-15.9. [Pg.420]


See other pages where 1.3- Butadiene benzene is mentioned: [Pg.241]    [Pg.262]    [Pg.391]    [Pg.63]    [Pg.157]    [Pg.157]    [Pg.321]    [Pg.234]    [Pg.234]    [Pg.292]    [Pg.2027]    [Pg.79]    [Pg.107]    [Pg.241]    [Pg.78]    [Pg.262]    [Pg.391]    [Pg.100]    [Pg.100]    [Pg.255]    [Pg.46]    [Pg.65]    [Pg.63]    [Pg.157]    [Pg.157]    [Pg.255]    [Pg.89]    [Pg.251]    [Pg.254]    [Pg.212]    [Pg.212]    [Pg.113]    [Pg.78]    [Pg.152]    [Pg.450]    [Pg.46]    [Pg.103]    [Pg.321]    [Pg.234]    [Pg.234]   
See also in sourсe #XX -- [ Pg.636 ]

See also in sourсe #XX -- [ Pg.636 ]




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Benzene 1,3-butadiene flame

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