FROM ALKANES

An alkene can be synthesized by the process of dehydrogenation (removal of hydrogen atoms), by heating an alkane up to about 700-750 . 

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Another name for aromatic hydrocarbons is arenes Arenes have properties that are much different from alkanes alkenes and alkynes The most important aromatic hydrocarbon... 

Bromination is normally used only to prepare tertiary alkyl bromides from alkanes... 

Chemical reactivity and functional group transformations involving the preparation of alkyl halides from alcohols and from alkanes are the mam themes of this chapter Although the conversions of an alcohol or an alkane to an alkyl halide are both classi tied as substitutions they proceed by very different mechanisms... 

All lation with Alkanes. Superacids such as HF-SbF abstract hydride ion from alkanes to form carbocations at low temperatures. The... 

Carbocations generated from alkanes using superacids react with carbon monoxide under mild conditions to form carboxyUc acid (188). In this process isomeric carboxyUc acids are produced as a mixture. However, when the reaction is mn with catalytic amounts of bromine (0.3 mmol eq) in HF-SbF solution, regio-selective carboxylation is obtained. / -Propane was converted almost exclusively to isobutyric acid under these conditions. 

Other gas-treating processes involving sulfolane are (/) hydrogen selenide removal from gasification of coal, shale, or tar sands (qv) (108) (2) olefin removal from alkanes (109) (J) nitrogen, helium, and argon removal from natural gas (110) (4) atmospheric CO2 removal in nuclear submarines (5) ammonia and H2S removal from waste streams (6) H2S, HCl, N2O, and CO2 removal from various streams (111—120) and (7) H2S and SO2 removal from... 

Both common and systematic names of compounds are used throughout this volume, depending on which the Editor-in-Chief feels is most appropriate. Preparations appear in the alphabetical order of names of the compound or names of the synthetic procedures. The Chemical Abstracts indexing name for each title compound, if it differs from the title name, is given as a subtitle. Because of the major shift to new systematic nomenclature adopted by Chemical Abstracts in 1972, many common names used in the text are immediately followed by the bracketed, new names. Whenever two names are concurrently in use, the carre CChemical Abstracts name is adopted. The prefix n- is deleted from -alkanes and w-alkyls. All reported dimensions are now expressed in S st me International units. 

As with alkyl and alkenyl substituents derived from alkanes and alkenes, respectively, alkynyl groups are also possible. 

Preparing Alkyl Halides from Alkanes Radical Halogenation 33B... 

The need to produce the carbohydrate moiety from alkane. 

Table 9.10 Examples of microbial products produced from alkanes and related compounds. Ail the examples cited are the subject of patents.

The difference in behaviour between pentyl and butyl cation systems (Figs. 3 and 4) has also been encountered in trapping experiments with carbonium ions, primarily formed from alkanes and SbFs, by CO (Hogeveen and Roobeek, 1972). In the case of n-butane the secondary butyloxocarbonium ion is the main product, whereas in the case of n-pentane only the tertiary pentyloxocarbonium ion is found. 

Neither methyl nor ethyl fluoride gave the corresponding cations when treated with SbFs. At low temperatures, methyl fluoride gave chiefly the methylated sulfur dioxide salt, (CH3OSO) ShF while ethyl fluoride rapidly formed the rert-butyl and ferf-hexyl cations by addition of the initially formed ethyl cation to ethylene molecules also formed ° At room temperature, methyl fluoride also gave the tert-butyl cation. In accord with the stability order, hydride ion is abstracted from alkanes by super acid most readily from tertiary and least readily from primary positions. 

The reaction mechanism involves carbonium and carbenium ion intermediates. The first and difficult step is the generation of carbonium ions from alkanes ... 

The activities of both haloalkanol dehalogenase (halohydrin hydrogen lyase) that catalyzes the formation of epoxides from alkanes with vicinal hydroxyl and halogen groups, and epoxide hydrolase that brings about hydrolysis of epoxyalkanes to diols are involved in a number of degradations that involve their sequential operation. 

D. Small, The Physical Chemistry of Lipids—from Alkanes to Phopholipids, Plenum Press, New York, 1986. 

Table 3 Grant and Paul parameters obtained from alkanes [80]...

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