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Fluorine boiling point

Figure 2.5 shows the boiling points of the hydrides in elements of Groups IV. V, VI and VII. Clearly there is an attractive force between the molecules of the hydrides of fluorine, oxygen and nitrogen... [Pg.52]

Fluorine is unique among the halogens m that increasing the number of fluorines does not lead to higher and higher boiling points... [Pg.150]

The physical properties of hydrofluorocarbons reflect their polar character, and possibly the importance of intermolecular hydrogen bonding (3). Hydrofluorocarbons often bod higher than either their PFC or hydrocarbon counterparts. For example, l-C H F bods at 91.5°C compared with 58°C for n-Q and 69°C for Within the series of fluorinated methanes, the boiling point reaches a maximum for CH2F2, which contains an equal... [Pg.282]

Properties. The physical properties of aHphatic fluorine compounds containing chlorine are similar to those of the PECs or HECs (3,5). They usually have high densities and low boiling points, viscosities, and surface tensions. The irregularity in the boiling points of the fluorinated methanes, however, does not appear in the chlorofluorocarbons. Their boiling points consistently increase with the number of chlorines present. The properties of some CECs and HCECs are shown in Tables 3 and 4. [Pg.284]

At 225—275°C, bromination of the vapor yields bromochloromethanes CCl Br, CCl2Br2, and CClBr. Chloroform reacts with aluminum bromide to form bromoform, CHBr. Chloroform cannot be direcdy fluorinated with elementary flourine fluoroform, CHF, is produced from chloroform by reaction with hydrogen fluoride in the presence of a metallic fluoride catalyst (8). It is also a coproduct of monochlorodifluoromethane from the HF—CHCl reaction over antimony chlorofluoride. Iodine gives a characteristic purple solution in chloroform but does not react even at the boiling point. Iodoform, CHI, may be produced from chloroform by reaction with ethyl iodide in the presence of aluminum chloride however, this is not the route normally used for its preparation. [Pg.524]

Murray, J. S., P. Lane, and P. Politzer. 1995b. Special Relationships of Fluorinated Methane/Ethane Boiling Points and Heats of Vaporization to Molecular Properties. J. Mol. Struct. (Theochem) 342, 15. [Pg.80]

It is an odourless, colourless, hygroscopic liquid, completely miscible with water in which it is hydrolysed at an appreciable rate with the loss of fluorine and loss of toxicity. It is about three times as toxic as tabun to most animal species. Its boiling-point, 147° with decomposition, classifies it as a semi-persistent gas. It is hydrolysed extremely rapidly by dilute aqueous... [Pg.105]

Perfluorinated alkanes and cycloalkanes are prepared from the corresponding hydrocarbons, either by electrochemical fluorination or by cobalt trifluoride fluo-rination [3], Many perfluorinated solvents are available commercially covering a wide selection of boiling points and densities. Some examples of perfluorinated solvents are listed in Table 3.1 together with their key physical properties. [Pg.58]


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See also in sourсe #XX -- [ Pg.10 ]




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