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Tetra- methane

Fluorocarbon-114 Fluorocarbon-21 1.2- Dichloro- Dichlorofluoro- 1.1.2.2- tetra- methane fluoroethane Fluorocarbon-113 1.1.2- Trichloro- 1.2.2- trifluoro-ethane... [Pg.217]

Methane is a tetrahedral molecule its four hydrogens occupy the corners of a tetra hedron with carbon at its center We often show three dimensionality m structural for mulas by using a solid wedge ) to depict a bond projecting from the paper toward you and a dashed wedge (i 111 ) for one receding away from you A simple line (—)... [Pg.29]

Water ammonia and methane share the common feature of an approximately tetra hedral arrangement of four electron pairs Because we describe the shape of a molecule according to the positions of its atoms rather than the disposition of its electron pairs however water is said to be bent and ammonia is trigonal pyramidal... [Pg.29]

Methane is the most difficult alkane to chlorinate. The reaction is initiated by chlorine free radicals obtained via the application of heat (thermal) or light (hv). Thermal chlorination (more widely used industrially) occurs at approximately 350-370°C and atmospheric pressure. A typical product distribution for a CH4/CI2 feed ratio of 1.7 is mono- (58.7%), di-(29.3%) tri- (9.7%) and tetra- (2.3%) chloromethanes. [Pg.138]

Malonic acid, amino-, diethyl ester, HYDROCHLORIDE, 40, 24 Malonic acid, bts(hydroxymethyl)-, DIETHYL ETHER, 40, 27 Malonitrile, condensation with tetra-cyanoethylene, 41, 99 2-Mercaptopyrimidine, 43, 6S hydrochloride of, 43, 68 Mercuric oxide in preparation of bromo-cyclopropane, 43, 9 Mesityl isocyanide, 41,103 5-Methallyl-l,2,3,4,5-pentachlorocyclo-pentadiene, 43, 92 Methane, dimesityl-, 43, 57 Methanesiileinyl chloride, 40, 62 Methanesulfonic acid, solvent for making peroxybenzoic acid from benzoic acid, 43, 93... [Pg.117]

When tetranuclear platinum complex (35) bridged by tetra(4-ethynylphenyl)-methane was used as the core (Fig. 6), dendrimers having more platinum atoms than those prepared from trinuclear platinum core 30 in the molecule were obtained up to the third generation. GPC analysis of these dendrimers revealed that the dendrimers with a tetraplatinum core have a similar molecular size to those with the triplatinum core 30. [Pg.54]

Similar reaction of 2,3,l, 3, 4, 6 -hexa-0-acetylsucrose with methane-sulfonyl chloride in N,N-dimethylformamide gave two products, which were separated on silica gel and characterized as 1,3,4,6-tetra-O - acetyl-/3 - D - fructofiiranosyl 2,3 - di - O - acetyl - 4,6 - dichloro -4,6 -... [Pg.263]

Tetra(3-aminopropanethiolato)trimercury perchlorate, 3582 Tetrakis(hydroxymercurio)methane, 0471 Trimercury tetraphosphide, 4616... [Pg.221]

Benzophenones are produced by the oxidation of diarylmethanes under basic conditions [6-9], The initial step requires a strongly basic medium to ionize the methane and the more lipophilic quaternary ammonium catalysts are preferred (Aliquat and tetra-n-octylammonium bromide are better catalysts than tetra-n-butyl-ammonium bromide). The oxidation and oxidative dehydrogenation of partially reduced arenes to oxo derivatives in a manner similar to that used for the oxidation of diarylmethanes has been reported, e.g. fluorene is converted into fluorenone (100%), and 9,10-dihydroanthracene and l,4,4a,9a-tetrahydroanthraquinone into anthraquinone (75% and 100%, respectively) [6]. [Pg.460]

Figure 4.6 Illustration of a covalent organic framework (COF) material composed of hexahydroxytriphenylene and either tetra(4-dihydroxyborylphenyl)methane or silane crosslinking moieties. (From Reference [56] with permission.)... Figure 4.6 Illustration of a covalent organic framework (COF) material composed of hexahydroxytriphenylene and either tetra(4-dihydroxyborylphenyl)methane or silane crosslinking moieties. (From Reference [56] with permission.)...
Treatment of fluorene, xanthene, thioxanthene, phenyl-4-pyridyl-methane, phenyl-2-pyridylmethane, 4,5-methylenephenanthrene, tetra-phenylcyclopentadiene, or phenalene with base and a trace of oxygen in DMSO (80% )-tert-buty alcohol (20%) solution gave significant amounts of the ketyls—i.e., Figure 6. These reactions may involve the initial formation of the ketone followed by reduction by the carbanion to yield the ketyl. [Pg.203]

Another and still more stabilized carbenium-phosphonium-oxonium-tetra-fluoroborate 225 can be prepared when bis-4.4- (l, l-dimethoxy-2.6-diphenyl-X -phosphorin)-methane 224 is treated with triphenylcarbenium-tetrafluoroborate. [Pg.131]

Chlorine or bromine reacts with alkanes in the presence of light (hv) or high temperatures to give alkyl halides. Usually, this method gives mixtures of halogenated compounds containing mono-, di-, tri- and tetra-halides. However, this reaction is an important reaction of alkanes as it is the only way to convert inert alkanes to reactive alkyl halides. The simplest example is the reaction of methane with CI2 to yield a mixture of chlorinated methane derivatives. [Pg.192]

Nitrosonium tetrafluoroborate has been prepared from nitrosyl fluoride (NOF) and boron trifluoride in Freon-113. With this reagent, in a nitro-methane solution, pyridine was converted into jV-nitrosopyridinium tetra-fluorobate, m.p. 155°-158°C [33]. [Pg.224]

The potential of the negative chemical-ionization (n.c.i.) technique for obtaining valuable structural information on very small samples of underivatized oligosaccharides has been demonstrated.200 The n.c.i. spectra of several mono-, di-, tri-, and tetra-saccharides were recorded, using methane as the reagent gas, and direct-probe insertion of the samples into the ion source.201 Fairly intense, molecular ions, M-, were observed in each case. A small number of fragment ions were also observed, but could not be interpreted. Use of dichlorodifluoro-... [Pg.262]


See other pages where Tetra- methane is mentioned: [Pg.298]    [Pg.235]    [Pg.250]    [Pg.196]    [Pg.189]    [Pg.80]    [Pg.166]    [Pg.225]    [Pg.431]    [Pg.930]    [Pg.295]    [Pg.183]    [Pg.196]    [Pg.319]    [Pg.311]    [Pg.145]    [Pg.137]    [Pg.24]    [Pg.72]    [Pg.202]    [Pg.128]    [Pg.242]    [Pg.264]    [Pg.199]    [Pg.17]    [Pg.66]    [Pg.86]    [Pg.165]    [Pg.16]    [Pg.229]    [Pg.163]   
See also in sourсe #XX -- [ Pg.9 , Pg.101 ]

See also in sourсe #XX -- [ Pg.385 ]

See also in sourсe #XX -- [ Pg.210 , Pg.215 ]

See also in sourсe #XX -- [ Pg.16 , Pg.17 ]

See also in sourсe #XX -- [ Pg.16 , Pg.17 ]




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Tetra chlor methane

Tetra phenyl methane

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