Ether groups group ratios

The photodecomposition of isopropyl alcohol on silica gel produces a seven-line spectrum having a hyperfine separation of 20.7 G and an amplitude ratio of 1 6.7 20.2 31 21.1 7.4 1.5 (68). This spectrum was attributed to SiOCMe2 formed from the ether surface groups. In addition to this spectrum the spectrum of the methyl radical was also observed. Irradiation of adsorbed tert-butyl alcohol produced a three-line spectrum which was attributed to SiOMe2OCH2 (68). Apparently the splitting from the methyl protons was too small to be observed. 

Two other myo-inositol derivatives have been selectively alkylated. Reaction of DL-l,2 4,5-di-0-cyclohexylidene-myo-inositol with benzyl chloride-potassium hydroxide in benzene, followed by removal of the acetal groups, gave DL-1-O- and DL-4-O-benzyl-myu-inositol in the ratio of 5 2, whereas, under similar conditions, DL-1,2 5,6-O-cyclohexylidene-myo-inositol gave311 the same ethers in the ratio of 57 10. These results are not readily explicable in the absence of knowledge of the conformations adopted by the cyclic acetals. 

For the reactions of MeLi with benzophenone and the benzophenone that was labeled at the carbon atom of the carbonyl group, ratio is 1.000 in ether at 0°C. Under the same conditions, this ratio is 1.023 for MeLi addition to the carbonyl pair of 2,4,6-trimethylbenzophenones... 

Figure 5 shows the XPS angular dependence of the fracture surface of a sample. The ratios of the ester carbonyl carbon and ether carbon to the total amount of carbon are plotted on the ordinate. The 30O angle means that the thickness measured is assumed to be about a half of that with an angle of 60°. The results show that the concentration of the ester bond observed on the interfacial substrate surface decreases toward the fracture interface, suggesting that the hydrocarbon groups are oriented toward the outside (lacquer side). The concentration of the ether group (a component of the lacquer) on the interfacial substrate surface is about one-third that on the interfacial lacquer surface, and it is presumed that the lacquer remained like islands on the substrate surface at an area ratio of 1 3. 

The DP is dependent on the ratio of reactants. Generally an excess of the epichlorohydrin is used to produce cyclic ether end groups. Epoxies are formed from the reaction of diamines with low molecular weight epoxy resins that retain their cyclic ether end groups. Figure 4.9 shows the formation of this process. These materials are often sold as two-part, or two-pot, epoxy adhesives. Most use-at-home epoxy packages contain a part A of epoxy resin and a part B of hardener (typically a diamine). These two are mixed as directed and applied. They dry fast, so they can be handled in 5 10 min. Full strength occurs after 5 7 days. 

Confirmation of these results was provided by a different laboratory67 in studies with allyl a-L-fucopyranoside. Partial benzylation of this compound, under conditions similar to those described previously,66 also gave the 2,4- and 3,4-dibenzyl ethers in the ratio of 3 2. In both publications, the structures assigned were primarily confirmed by methylation of unreacted hydroxyl groups with methyl iodide-sodium hydride in dimethyl sulfoxide,68 followed by catalytic debenzylation, and isolation and characterization of the known methyl ethers. 

Monomolar benzylation of methyl 2,3-di-0-benzyl-a-D-galactopyranoside in DMF gave 2,3,6-tri-O-benzyl derivative in 73% yield [52], The primary 6-benzyl ether also forms the major part of the monobenzyl fraction obtained from methyl a-D-galactopyranoside or from its p-anomer [53]. Interestingly, position 6 becomes less reactive than position 2 if 3,4-0-isopropylidene acetals is used to protect the other two secondary hydroxyl groups. The ratio of 2- and 6-benzyl ethers was found to be 11 1 in the a-anomer and 2.5 1 in the p-anomer [53] (see also, Ref. [54]). Uridine [55], cyti-dine [56], and 4-(methylthio)uridine [56] also prefer OH-2 over the primary position when benzylated in dimethyl sulfoxide (for other benzylations in this solvent, see Refs. [35, 57]). 

The hemicelluloses of wood contain uronic acid residues which frequently bear methyl ether groups. Hydrolysis of the hemicelluloses yields aldobioLironic and aldotriouronic acids. In researches referred to previously (page 300), O Dwyer " investigated the hemicelluloses from oakwood. She isolated an aldobiouronic acid as a barium salt after combined enzymic and acidic hydrolysis. Analyses of this compound were in agreement with the empirical formula for a barium salt of an 0-methyl-xylo-aldobiouronic acid. This compound was isolated from a polysaccharide material which contained xylose (6 parts), uronic acid (1 part), and methoxyl (1 part). Studies by Anderson on the hemicelluloses of a number of hardwoods also showed that 0-methylhexuronic acid residues are present in glycosidic union with xylose, in ratios extending from 8 to 19 xylose units per uronic acid unit. 

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