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Methanol structure

Figure 15 The (12)- (methanol) structure projected in the be plane and showing the parallel layers of opposite chirality. Hydrogen atoms are omitted for clarity. Figure 15 The (12)- (methanol) structure projected in the be plane and showing the parallel layers of opposite chirality. Hydrogen atoms are omitted for clarity.
FIGURE 14.9 Absorption (a) and fluorescence (b) spectra of m-PPE-S03 in methanol, water, and methanol/water mixtures. Labels indicate spectra in pure water and methanol. Structure of m-PPE-S03 shown at upper right. [Pg.571]

Square planar Co (II) complexes contain ligands in the axial positions coordinated to the metal. The nature of these ancillary ligands depends on the synthetic route. For example, if the product is purified by a recrystallization in methanol, then the axial ligands will be methanol, structures 18 and 19. [Pg.258]

Prepared generally by ester interchange from polyvinylacelate (ethanoate) using methanol and base also formed by hydrolysis of the acetate by NaOH and water. The properties of the poly(vinyl alcohol) depend upon the structure of the original polyvinyl acetate. Forms copolymers. Used as a size in the textile industry, in aqueous adhesives, in the production of polyvinyl acetates (e.g. butynal) for safety glasses. U.S. production 1980... [Pg.323]

For methanol clusters [36], it was found that the dimer is linear, while clusters of 3 and 4 molecules exist as monocyclic ring structures. There also is evidence that there are two cyclic ring trimer confomiers in the molecular beam. [Pg.1170]

Physical properties of A-4-thiazoline-2-one and derivatives have received less attention than those of A-4-thiazoline-2-thiones. For the protomeric equilibrium, data obtained by infrared spectroscopy favors fbrm 51a in chloroform (55, 96, 887) and in the solid state (36. 97. 98) (Scheme 23). The same structural preference is suggested by the ultraviolet spectroscopy studies of Sheinker (98), despite the fact that previous studie.s in methanol (36) suggested the presence of both 51a and... [Pg.387]

Suggest a structure for the product of nucleophilic substitution obtained on solvolysis of tert-butyl bromide in methanol and outline a reason able mechanism for its formation... [Pg.340]

Hydrolysis of a compound A in dilute aqueous hydrochlonc acid gave (along with methanol) a compound B mp 164—165°C Compound B had the molecular formula CigHig04 it exhibited hydroxyl absorption in its IR spectrum at 3550 cm but had no peaks in the carbonyl region What IS a reasonable structure for compound B" ... [Pg.750]

Pentafluoro 6 nitrobenzene reacts readily with sodium methoxide m methanol at room temperature to yield two major products each having the molecular formula C7H3F4NO3 Suggest reasonable structures for these two compounds... [Pg.989]

Write structural formulas for the a and 3 methyl pyranosides formed by reaction of o galactose with methanol in the presence of hydrogen chloride... [Pg.1045]

The use of penodic acid oxidation m structure determination can be illustrated by a case m which a previously unknown methyl glycoside was obtained by the reaction of D arabmose with methanol and hydrogen chlonde The size of the nng was identified as five membered because only one mole of penodic acid was consumed per mole of glycoside and no formic acid was produced Were fhe nng six membered fwo moles of penodic acid would be required per mole of glycoside and one mole of formic acid would be produced... [Pg.1060]

Methanol, which elutes at 4.69 min, is included as a neutral species to indicate the electroosmotic flow. When using standard solutions of each vitamin, CZE peaks are found at 3.41 min, 4.69 min, 6.31 min, and 8.31 min. Examine the structures and p/Ca information in Figure 12.47, and determine the order in which the four B vitamins elute. [Pg.607]

The UV spectra of quinoxalines have been examined in several solvents. In cyclohexane, three principal absorptions are observed (Table 2). In hydroxylic solvents the vibrational fine structure disappears and in methanol or water the weak n- ir transitions are obscured by the intense ir->ir transition (79HC(35)l). [Pg.161]

Oxetane-2-methanol, t/ireo-a,3,3,4,4-pentamethyl-3,5-dinitrobenzoate X-ray crystal structure, 7, 365 Oxetane-3-methanol, 3-alkyl-reactions... [Pg.733]

A compound with the elemental composition C15//22O3 was isolated from the methanol extract of the Chilean medicinal plant Centaurea chilensis (Compositae)What is the structure of the natural product, given the NMR experiments 47 ... [Pg.142]

Surface SHG [4.307] produces frequency-doubled radiation from a single pulsed laser beam. Intensity, polarization dependence, and rotational anisotropy of the SHG provide information about the surface concentration and orientation of adsorbed molecules and on the symmetry of surface structures. SHG has been successfully used for analysis of adsorption kinetics and ordering effects at surfaces and interfaces, reconstruction of solid surfaces and other surface phase transitions, and potential-induced phenomena at electrode surfaces. For example, orientation measurements were used to probe the intermolecular structure at air-methanol, air-water, and alkane-water interfaces and within mono- and multilayer molecular films. Time-resolved investigations have revealed the orientational dynamics at liquid-liquid, liquid-solid, liquid-air, and air-solid interfaces [4.307]. [Pg.264]

One class of materials with some inherent PSA properties includes polyvinyl-ethers. Vinyl ether monomers are industrially derived from the reaction of acetylene with alcohols [117]. The most common alcohols used are methanol, ethanol or isobutanol. A generic structure of the vinyl ether is shown below ... [Pg.509]

From their structures, it appears that the hydrolytic stability of macrocyclic lactones must necessarily be inferior to macrocyclic polyethers. Ease of synthesis of the cyclic esters is therefore one of the aspects which commend them to interest. It is probably for this reason that such lactones have not been made more often by the interesting approach of Kdgel and Schroder . These workers report the ozonolysis of dibenzo-18-crown-6 in a mixture of methanol and dichloromethane at —20°. Reduction of the ozon-ide at —75° using dimethylsulfide followed by warming and addition of acetone led to formation of 6 in 14% yield. The bis-oxalate had mp 164—165° from acetone, very similar to that of the starting crown. The transformation is illustrated below in Eq. (5.9). [Pg.225]

The methacrylic backbone structure makes the spherical Toyopearl particles rigid, which in turn allows linear pressure flow curves up to nearly 120 psi (<10 bar), as seen in Fig. 4.45. Toyopearl HW resins are highly resistant to chemical and microbial attack and are stable over a wide pH range (pH 2-12 for operation, and from pH 1 to 13 for routine cleaning and sanitization). Toyopearl HW resins are compatible with solvents such as methanol, ethanol, acetone, isopropanol, -propanol, and chloroform. Toyopearl HW media have been used with harsh denaturants such as guanidine chloride, sodium dodecyl sulfate, and urea with no loss of efficiency or resolution (40). Studies in which Toyopearl HW media were exposed to 50% trifluoroacetic acid at 40°C for 4 weeks revealed no change in the retention of various proteins. Similarly, the repeated exposure of Toyopearl HW-55S to 0.1 N NaOH did not change retention times or efficiencies for marker compounds (41). [Pg.150]

Although the structure of [SsN] has not been established by X-ray crystallography, the vibrational spectra of 30% N-enriched [SsN] suggest an unbranched [SNSS] (5.22) arrangement of atoms in contrast to the branched structure (Dsh) of the isoelectronic [CSs] and the isovalent [NOs] ion (Section 1.2). Mass spectrometric experiments also support the SNSS connectivity in the gas phase.Many metal complexes are known in which the [SsN] ion is chelated to the metal by two sulfur atoms (Section 7.3.3). Indeed the first such complex, Ni(S3N)2, was reported more than twenty years before the discovery of the anion. It was isolated as a very minor product from the reaction of NiCl2 and S4N4 in methanol. However, some of these complexes, e.g., Cu and Ag complexes, may be obtained by metathetical reactions between the [S3N] ion and metal halides. [Pg.100]

Enamines formed in this way may be distilled or used in situ. The ease of formation of the enamine depends on the structure of the secondary amine as well as the structure of the ketone. Thus pyrrolidine reacts faster than morpholine or piperidine, as expected from a rate-controlling transition state with imonium character. Six-membered ring ketones without a substituents form pyrrolidine enamines even at room temperature in methanol (20), and morpholine enamines are generated in cold acetic acid (21), but a-alkylcyclohexanones, cycloheptanone, and linear ketones react less readily. In such examples acid catalysis with p-toluenesulfonic acid or... [Pg.315]


See other pages where Methanol structure is mentioned: [Pg.462]    [Pg.134]    [Pg.49]    [Pg.179]    [Pg.280]    [Pg.49]    [Pg.47]    [Pg.280]    [Pg.462]    [Pg.134]    [Pg.49]    [Pg.179]    [Pg.280]    [Pg.49]    [Pg.47]    [Pg.280]    [Pg.588]    [Pg.567]    [Pg.335]    [Pg.29]    [Pg.145]    [Pg.290]    [Pg.129]    [Pg.537]    [Pg.689]    [Pg.1062]    [Pg.280]    [Pg.23]    [Pg.73]    [Pg.466]    [Pg.989]    [Pg.128]   
See also in sourсe #XX -- [ Pg.238 ]

See also in sourсe #XX -- [ Pg.402 ]

See also in sourсe #XX -- [ Pg.319 ]

See also in sourсe #XX -- [ Pg.281 , Pg.282 ]




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