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Halogens melting points

Halogen Melting point (°C) Boiling point (°C) Vapour density (air = 1.0) Threshold limit value (ppm) Reactivity and oxidizing strength Appearance and state at 21 " C Colour of gas/vapour... [Pg.133]

Lithium Halides. Lithium haHde stabiHty decreases with increasing atomic weight of the halogen atom. Hence, the solubiHty increases from the sparingly soluble Hthium fluoride to the very soluble bromide and iodide salts. The low melting points of Hthium haHdes are advantageous for fluxes in many appHcations. [Pg.225]

Dihydroquinazolines are normally stable compounds but they deteriorate on long standing. Some examples are known to oxidize to the corresponding 4(3H)quinazolinones. 3-Methyl-3,4-dihydroquin-azoline is converted to the 4-oxo compound after three recrystallizations from light petroleum. The most remarkable example is 3,4-dihydro-6-fluoro-3(p-fluorophenyl)quinazoline [(44), R = F] which oxidizes at its melting point (137°-I38°C), Other halogenated derivatives of (44) are more stable. ... [Pg.285]

A mixture of 12.6 g of benzoyl chloride in 100 cc of ethylene chloride is added dropwise to a suspension of 25.6 g of 3ethylene chloride and 21.8 g of triethylamine within 18 minutes at room temperature while stirring. The mixture is stirred at room temperature for a further 14 hours, 200 cc of water are added, the organic phase is separated and concentrated to an oil in a vacuum. Upon adding ether/dimethoxy ethane to this oil, crude 6-ben zoy I-3absolute ethanol with the addition of a small amount of coal, the compound has a melting point of 125°C to 127°C (decomp.). Displacement of the halogen with hydrazine leads to the formation of endralazine. [Pg.557]

In this context, the use of ionic liquids with halogen-free anions may become more and more popular. In 1998, Andersen et al. published a paper describing the use of some phosphonium tosylates (all with melting points >70 °C) in the rhodium-catalyzed hydroformylation of 1-hexene [13]. More recently, in our laboratories, we found that ionic liquids with halogen-free anions and with much lower melting points could be synthesized and used as solvents in transition metal catalysis. [BMIM][n-CgHi7S04] (mp = 35 °C), for example, could be used as catalyst solvent in the rhodium-catalyzed hydroformylation of 1-octene [14]. [Pg.216]

How do the trends in physical properties for the halogens compare with those for the inert gases Compare boiling points, melting points, and atomic volumes. [Pg.105]

Table 19-11. sizes of the halogen atoms, melting points, boiling points, AND DISSOCIATION PROPERTIES OF THE HALOGEN MOLECULES... [Pg.355]

Self-Test 15.5B Explain the trends in the melting points and boiling points of the halogens. [Pg.761]

Chemical Resistance. TiC oxidizes slowly in air at 800°C. It is resistant to most acids. It is attacked by HNO3, HF, and the halogens. It can be heated in hydrogen to its melting point without decomposition. [Pg.251]

For single crystals, the same method is applied, using an excess of metal and of halogen. After reaction, the mixture of the sulfide halide and the halide is heated to a temperature slightly above the melting point of the respective halide. Perfect, small crystals for X-ray determination are formed. The excess of the trihalide is removed by treatment with anhydrous alcohol 92, 93, 96). CeSI may also be prepared from the sulfides 68, 93) CeSCl is formed by reaction 4 92). [Pg.359]

In general, the electrolysis of a molten salt at inert electrodes produces the metal at the cathode, e.g., calcium from calcium chloride (melting point 774 °C). The anion is often a halide ion which, on discharge, yields the halogen, e.g., chlorine from calcium chloride. [Pg.708]


See other pages where Halogens melting points is mentioned: [Pg.1026]    [Pg.490]    [Pg.482]    [Pg.292]    [Pg.336]    [Pg.461]    [Pg.8]    [Pg.652]    [Pg.656]    [Pg.774]    [Pg.838]    [Pg.862]    [Pg.873]    [Pg.476]    [Pg.1110]    [Pg.240]    [Pg.429]    [Pg.916]    [Pg.97]    [Pg.100]    [Pg.462]    [Pg.65]    [Pg.256]    [Pg.440]    [Pg.206]    [Pg.86]    [Pg.360]    [Pg.1026]    [Pg.131]    [Pg.109]    [Pg.474]    [Pg.504]    [Pg.184]    [Pg.28]    [Pg.441]   
See also in sourсe #XX -- [ Pg.208 ]




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