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Alkylation continued

If any feedstock other than alkylate is currently being used, switch supply to alkylate and recirculate the alkylate continuously around the reactor until all the remaining SO3 has been consumed. [Pg.213]

Ccxnplexes containing DAB ligands (RN=CHCH=NR R=alkyl) continue to be explored. Reactions between Fe2(CO) and [Fe(CO) (DAB)] lead to [Fe2(CO)g(DAB)] products containing six-eiectron donor DAB. [Pg.196]

For b the Diels-Alder now looks best. For c alkylation with the aUyl hafide looks good. There are of course other solutions, but continue the analysis along these lines. [Pg.123]

Branched alkyl groups are named by using the longest continuous chain that begins at the point of attachment as the base name Thus the systematic names of the two C3H7 alkyl groups are propyl and 1 methylethyl Both are better known by their common names n propyl and isopropyl respectively... [Pg.74]

The lUPAC rules permit alkyl halides to be named m two different ways called func twnal class nomenclature and substitutive nomenclature In functional class nomencla ture the alkyl group and the halide (fluoride chloride bromide or iodide) are desig nated as separate words The alkyl group is named on the basis of its longest continuous chain beginning at the carbon to which the halogen is attached... [Pg.144]

Representative Functional Group Transformations by Nucleophilic Substitution Reactions of Alkyl Halides (Continued)... [Pg.329]

In a similar manner competitive alkylation may continue resulting m formation of a trialkylamme... [Pg.929]

For branching compounds, the parent structure is the longest continuous chain present in the compound. Consider the compound to have been derived from this structure by replacement of hydrogen by various alkyl groups. Arabic number prefixes indicate the carbon to which the alkyl group is attached. Start numbering at whichever end of the parent structure that results in the lowest-numbered locants. The arable prefixes are listed in numerical sequence, separated from each other by commas and from the remainder of the name by a hyphen. [Pg.2]

TABLE 7.51 Effect of Substituent Groups on Alkyl Chemical Shifts Continued)... [Pg.792]

Dialkylaminoethyl acryhc esters are readily prepared by transesterification of the corresponding dialkylaminoethanol (102,103). Catalysts include strong acids and tetraalkyl titanates for higher alkyl esters and titanates, sodium phenoxides, magnesium alkoxides, and dialkyitin oxides, as well as titanium and zirconium chelates, for the preparation of functional esters. Because of loss of catalyst activity during the reaction, incremental or continuous additions may be required to maintain an adequate reaction rate. [Pg.156]

The first resins to be produced on a commercial scale were the coumarone—indene or coal-tar resins (1) production in the United States was started before 1920. These resins were dominant until the development of petroleum resins, which were estabHshed as important raw materials by the mid-1940s. Continued development of petroleum-based resins has led to a wide variety of aHphatic, cyclodiene, and aromatic hydrocarbon-based resins. The principal components of petroleum resins are based on piperylenes, dicyclopentadiene (DCPD), styrene, indene, and their respective alkylated derivatives. [Pg.350]

A iridine traces in aqueous solution can be determined by reaction with 4-(p-nitroben25l)pyridine [1083-48-3] and potassium carbonate [584-08-7]. Quantitative determination is carried out by photometric measurement of the absorption of the blue dye formed (367,368). Alkylating reagents interfere in the determination. A iridine traces in the air can be detected discontinuously by absorption in Folin s reagent (l,2-naphthoquinone-4-sulfonate) [2066-93-5] (369,370) with subsequent chloroform extraction and hplc analysis of the red dye formed (371,372). The detection limit is ca 0.1 ppm. Nitrogen-specific thermal ionisation detectors can be used for continuous monitoring of the ambient air. [Pg.12]

Phosphate ester fluids are the most fire resistant of moderately priced lubricants, are generally excellent lubricants, and are thermally and oxidatively stable up to 135°C (38). Fire-resistant iadustrial hydrauHc fluids represent the largest volume commercial use. AppHcations are made ia air compressors and continue to grow for aircraft use (tributyl and/or an alkyl diaryl ester) and ia hydrauHc control of steam turbiaes ia power generation (ISO 46 esters). [Pg.246]

Figure 4c illustrates interfacial polymerisation encapsulation processes in which the reactant(s) that polymerise to form the capsule shell is transported exclusively from the continuous phase of the system to the dispersed phase—continuous phase interface where polymerisation occurs and a capsule shell is produced. This type of encapsulation process has been carried out at Hquid—Hquid and soHd—Hquid interfaces. An example of the Hquid—Hquid case is the spontaneous polymerisation reaction of cyanoacrylate monomers at the water—solvent interface formed by dispersing water in a continuous solvent phase (14). The poly(alkyl cyanoacrylate) produced by this spontaneous reaction encapsulates the dispersed water droplets. An example of the soHd—Hquid process is where a core material is dispersed in aqueous media that contains a water-immiscible surfactant along with a controUed amount of surfactant. A water-immiscible monomer that polymerises by free-radical polymerisation is added to the system and free-radical polymerisation localised at the core material—aqueous phase interface is initiated thereby generating a capsule sheU (15). [Pg.320]


See other pages where Alkylation continued is mentioned: [Pg.147]    [Pg.146]    [Pg.235]    [Pg.147]    [Pg.146]    [Pg.235]    [Pg.158]    [Pg.2790]    [Pg.464]    [Pg.899]    [Pg.161]    [Pg.23]    [Pg.168]    [Pg.75]    [Pg.178]    [Pg.220]    [Pg.234]    [Pg.135]    [Pg.318]    [Pg.449]    [Pg.552]    [Pg.266]    [Pg.429]   


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Aldehydes continued alkylation reactions

Alkyl chloride alkylation (continued

Alkyl halides—continued

Alkyl halides—continued reactions

Alkyl halides—continued synthesis

Alkyl halides—continued tertiary

Alkylation reactions continuous

Catalysis continued alkyl halides

Catalysis continued alkylation

Continuous isobutane alkylation

Cyclohexanone—continued alkylation

Friedel-Crafts alkylation continued)

Pyridine, reactions with—continued alkylation

Pyridine, reactions with—continued alkyls

Pyridones, 1 -alkyl—continued

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