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Normal temperature

Cumulenic anions, C=C=C and C=C=C=C, without strongly electron-withdrawing substituents are much stronger bases than acetylides, "CsC- and are therefore also stronger nucleophiles. In view of the poor stability of the cumulenic anions at normal temperatures this is a fortunate circumstance the usual functionalization reactions such as alkylation, trimethylsilylation and carboxylation in most cases proceed at a sufficient rate at low temperatures, provided that the... [Pg.27]

Thermal energy in flame atomization is provided by the combustion of a fuel-oxidant mixture. Common fuels and oxidants and their normal temperature ranges are listed in Table 10.9. Of these, the air-acetylene and nitrous oxide-acetylene flames are used most frequently. Normally, the fuel and oxidant are mixed in an approximately stoichiometric ratio however, a fuel-rich mixture may be desirable for atoms that are easily oxidized. The most common design for the burner is the slot burner shown in Figure 10.38. This burner provides a long path length for monitoring absorbance and a stable flame. [Pg.413]

Application of an electric field between two metal electrodes causes a few ions and electrons to be desorbed and is surface or thermal emission (see Chapter 7 for more information on thermal ionization). Unless the electrodes are heated strongly, the number of electrons emitted is very small, but, even at normal temperatures, this emission does add to the small number of electrons caused by cosmic radiation and is continuous. [Pg.40]

As excited atoms, molecules, or ions come to equilibrium with their surroundings at normal temperatures and pressures, the extra energy is dissipated to the surroundings. This dissipation causes the particles to slow as translational energy is lost, to rotate and vibrate more slowly as rovibrational energy is lost, and to emit light or x-rays as electronic energy is lost. [Pg.387]

The loss of energy returns the particles to their original (ground) state, viz., their energy state at normal temperatures and pressures. [Pg.387]

If the spectmm is observed in absorption, as it usually is, and at normal temperatures the intensities of the transitions decrease rapidly as v" increases, since the population of the uth vibrational level is related to Nq by the Boltzmann factor... [Pg.139]

The combination of durability and clarity and the ability to tailor molecules relatively easily to specific applications have made acryflc esters prime candidates for numerous and diverse applications. At normal temperatures the polyacrylates are soft polymers and therefore tend to find use in applications that require flexibility or extensibility. However, the ease of copolymerizing the softer acrylates with the harder methacrylates, styrene, acrylonitrile, and vinyl acetate, allows the manufacture of products that range from soft mbbers to hard nonfilm-forming polymers. [Pg.171]

Liquefied natural gas (LNG) also plays a large role in both the transportation and storage of natural gas. At a pressure of 101.3 kPa (1 atm), methane can be Hquefted by reducing the temperature to about — 161°C. When in the Hquid form, methane occupies approximately 1/600 of the space occupied by gaseous methane at normal temperature and pressure. In spite of the very low temperature of the Hquid, LNG offers advantages for both shipping and storing natural gas. [Pg.173]

Fourier s Law of Heat Conduction. The heat-transfer rate,, per unit area,, in units of W/m (Btu/(ft -h)) transferred by conduction is directly proportional to the normal temperature gradient ... [Pg.481]

Tetrasubstituted and some hindered trisubstituted alkenes react rapidly only to the monoalkylborane stage. Rarely, when the tetrasubstituted double bond is incorporated in a cycHc stmcture, does hydroboration under normal conditions fail (25—27). However, such double bonds may react under conditions of greater force (25,28—31). Generally, trialkylboranes are stable at normal temperatures, undergoing thermal dissociation at temperatures above 100°C (32—34). In the presence of B—H bonds, trialkylboranes undergo a redistribution reaction (35—38). [Pg.308]

Vinyl chloride (also known as chloroethylene or chloroethene) is a colorless gas at normal temperature and pressure, but is typically handled as the hquid (bp —13.4° C). However, no human contact with the Hquid is permissible. Vinyl chloride is an OSHA-regulated material. [Pg.413]

Table 7. Cement Phases Hydrated at Normal Temperatures ... Table 7. Cement Phases Hydrated at Normal Temperatures ...
Various catalytic materials promote dehydrochlorination including AlCl (6,91), AICk-nitrohenzene complex (114), activated alumina (3), and FeCl (112). Chlorination in the presence of anhydrous aluminum chloride gives hexachloroethane. Dry pentachloroethane does not corrode iron at temperatures up to 100°C. It is slowly hydrolyzed by water at normal temperatures and oxidized in the presence of light to give trichloroacetyl chloride. [Pg.14]

Contact with eye tissue at normal temperatures causes pain, mild to moderate irritation, and possibly some transient corneal injury. Prompt washing with large quantities of water is helpful in minimizing the adverse effects of eye exposure. [Pg.48]

As in the case of hydrogen and tritium, deuterium exhibits nuclear spin isomerism (see Magnetic spin resonance) (14). However, the spin of the deuteron [12597-73-8] is 1 instead of S as in the case of hydrogen and tritium. As a consequence, and in contrast to hydrogen, the ortho form of deuterium is more stable than the para form at low temperatures, and at normal temperatures the ratio of ortho- to para-deuterium is 2 1 in contrast to the 3 1 ratio for hydrogen. [Pg.3]

The overall picture of the many results which have been obtained with hetero-substituted cyclohexane rings is a very consistent one. Cyclohexane itself in its lowest energy conformation adopts the so-called chair conformation, as depicted in Figure 3 by the two outer formulae (a, b). These are contained in energy wells ca. 42 kJ moP deep. Another conformation, of low abundance in cyclohexane at normal temperatures, but which is important in some substituted derivatives, is the twist form (c, d). This is ca. 22 kJ moP less stable than the chair forms, and it lies on the lowest-energy pathway between them. [Pg.8]

Diazirines tend to decompose, in some cases without obvious cause. Gaseous methyl-diazirine exploded at normal temperature and liquid a-hydroxyethylmethyldiazirine exploded on taking it from a dry ice bath 67CB2093). Phenylchlorodiazirine is reported to be more shock sensitive than nitroglycerol 79AHC(24)63). [Pg.223]


See other pages where Normal temperature is mentioned: [Pg.24]    [Pg.152]    [Pg.282]    [Pg.282]    [Pg.290]    [Pg.16]    [Pg.160]    [Pg.482]    [Pg.16]    [Pg.43]    [Pg.131]    [Pg.219]    [Pg.379]    [Pg.508]    [Pg.567]    [Pg.16]    [Pg.493]    [Pg.533]    [Pg.3]    [Pg.117]    [Pg.64]    [Pg.67]    [Pg.441]    [Pg.461]    [Pg.279]    [Pg.579]    [Pg.398]    [Pg.474]    [Pg.523]    [Pg.2]    [Pg.364]    [Pg.362]    [Pg.364]    [Pg.1059]   
See also in sourсe #XX -- [ Pg.3 ]




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