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Polar acids

Sandarac. This resin, which originates in Morocco, is a polar, acidic, hard resin with a softening point of 100—130°C, an acid number of 117—155, and a saponification number of 145—157. Sandarac [9000-57-1] is soluble in alcohols and insoluble in aryl and aUphatic hydrocarbons. It is used in varnishes and lacquers for coating paper, wood, and metal. [Pg.140]

Probably the most common distillation method used as a form of sample preparation for chromatographic analysis is steam distillation [31,32]. Solvent extraction and gas phase stripping methods are generally inefficient procedures for isolating polar, acidic, or basic compounds in an aqueous matrix due to the low efficiency of water immiscible solvents for the extraction of these compounds and their low volatility and high water affinity which results in a very slow transfer to the gas phase using... [Pg.886]

One of the main problems of the pyrolysis technique is related to the low volatility of pyrolysis products arising from natural and some synthetic macromolecules. In fact, the polar acidic, alcoholic and aminic moieties are not really suitable for gas chromatographic analysis. Their poor volatility and their polarity cause a rather low reproducibility of the pyrograms, low sensitivity for specific compounds, and strong memory effects. Memory effects need to be borne in mind when the pyrolysis of polar molecules is performed. Polar pyolysis products may not be completely eluted by the gas chromatographic column, and... [Pg.304]

Similar to the studies conducted in The Netherlands and Germany, NPEOs and NP were found in both water and sediment samples, while more polar acidic metabolites (NPEiC) were detected only in water samples (Figs. 6.2.3 and 6.2.4). [Pg.716]

The above examples show that a very important criterion in the choice of a probe is its sensitivity to a particular property of the microenvironment in which it is located (e.g. polarity, acidity, etc.). On the other hand, insensitivity to the chemical nature of the environment is preferable in some cases (e.g. in fluorescence polarization or energy transfer experiments). Environment-insensitive probes are also better suited to fluorescence microscopy and flow cytometry. [Pg.15]

Note This reaction involves a polar acidic mechanism, not a free-radical mechanism It is a Friedel-Crafts alkylation, with the slight variation that the requisite carbocation is made by protonation of an alkene instead of ionization of an alkyl halide. Protonation of C4 gives a C3 carbocation. Addition to Cl and fragmentation gives the product. [Pg.125]

Step 3. The numbering of the atoms in this polar acidic mechanism is not straightforward, because it is... [Pg.126]

Using these optimized conditions, the conjugate addition of 45 to the malonates 49 in the presence of the solid base provided access to the Michael adducts in good yields and high diastereoselectivities. The removal of the chiral TADDOL auxiliary could be accomplished without epimerization or racemization in this case, too. After esterification of the very polar acid intermediates with diazomethane the corresponding dimethyl esters 52 were obtained with yields of 72-94% and enantiomeric excesses ee of 84-94% (Scheme 1.1.13). [Pg.13]

The physical solvent-based acid-gas removal systems do not rely upon the acidic properties of the acid gas. Rather, the polar acid gases have a much greater solubility in many oils and solvents, compared with fuel gas species. [Pg.29]

Homology modelling is not an exact technique. Especially, when the extent of sequence homology (exact matches and matches between amino acid residues of similar property, e.g. hydrophobic, polar, acidic, basic) is low, then more attention will be paid to structural rather than sequence similarities and to prediction of structure for unmatched sequences. In such cases, and always when there is no crystal structure of a member of the family to provide a template, then total reliance has to be placed on the experience of the investigator or in one of the many computer programs now available. The principal methods have been reviewed by Sternberg (1986) and Blundell et al. (1987a). [Pg.113]

The choice of ethanol or acetonitrile depends upon the type of sample however, most samples can be analyzed using either solvent. The main difference would be that ethanol will extract the more highly polar acids better than acetonitrile. [Pg.1125]

The results of the infrared analysis are presented in Table VI. These results show that carboxylic acids and phenols are found only in the acid concentrates. Carboxylic acids are concentrated in the polar acid subfractions III and IV while phenols are concentrated in subfraction II. Carbazoles, ketones, and amides are found in all three major nonhydrocarbon fractions. The appearance of the same compound type in several fractions may arise from differences in acidity or basicity that are caused by the hydrocarbon portion of the molecule. Multifunctionality could also be a factor in the distribution of compound types among the fractions. The 1695 cm"1 band was assigned to ketones on the basis of work... [Pg.136]

C is correct The solubilities of amino acids differ based upon the R group. Phenylalanine has a benzene R group and is the least polar amino acid listed. The carboxylic acid and amines on the other R groups increase solubility. You may have also memorized the four groups of amino acid side chains as either nonpolar, polar, acidic, or basic. Acidic, basic, and polar amino adds have greater water sohibility than nonpolar amino acids. [Pg.147]

Overall, a large variability in Koc values was observed, especially for the more polar compounds. For relatively nonpolar esters, Koc was considered a useful model for sorption to soil with high organic carbon and low clay content, with variation by a factor of 3-5. Significant correlations between Koc and molecular size, self polarizability, and MCIs were observed. For polar acids and amines, Koc values varied up to two orders of magnitude, and poor correlations were obtained for most of the parameters examined. [Pg.183]

Silica—Particles or spheres of crystalline silicic acid used in chromatography. Its surface is polar, acidic, and tends to attract water of hydration and polar compounds. [Pg.218]

Very polar (acidic) Polyethyleneglycol ester AT-1000, FFAP, Nukol, OV-351, SP-1000, Superox-FA... [Pg.35]


See other pages where Polar acids is mentioned: [Pg.541]    [Pg.168]    [Pg.374]    [Pg.15]    [Pg.368]    [Pg.186]    [Pg.20]    [Pg.25]    [Pg.92]    [Pg.1240]    [Pg.9]    [Pg.9]    [Pg.11]    [Pg.13]    [Pg.7]    [Pg.672]    [Pg.30]    [Pg.82]    [Pg.330]    [Pg.103]    [Pg.138]    [Pg.368]    [Pg.29]    [Pg.185]    [Pg.186]    [Pg.10]    [Pg.1119]    [Pg.787]    [Pg.948]    [Pg.948]    [Pg.570]    [Pg.81]    [Pg.184]   
See also in sourсe #XX -- [ Pg.590 ]




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Acid chloride polarity

Acidic polar side chains

Acidity polar reactions

Acids polarity

Acids polarity

Amides, from acid derivatives polarity

Amino acid uncharged, polar

Amino acids group 2- electrically neutral polar side chains

Amino acids polar

Amino acids polar side chains

Amino acids polar, hydrophilic

Amino acids polarity

Anodic polarization curves sulfuric acid

Bile acid glucuronides polarity

Bile acid sulfates polarity

Biotic Dicarboxylic Acids CCC Separation with Polar Two-Phase Solvent Systems using a Cross-Axis Coil Planet Centrifuge Kazufusa Shinomiya and Yoichiro Ito

Carbonyl compound , acidity polarity

Carboxylic acid derivative polarity

Carboxylic acid polarity

Deoxyribonucleic acid, polar

Hydrochloric acid polar molecule

Hydrothermal Conversion of Waste Polarizing Film to Acetic Acid

Lewis acids with polar multiple bonds

Ligand binding amino acids, polar

Nucleic acid polarity

Polar Covalent Bonds Acids and Bases

Polar acidic amino adds

Polar acidic nitrosamines

Polar basic amino acids

Polar carboxylic acids

Polar neutral amino acids, ionized forms

Polar reaction with Lewis acids

Polar reactions under acidic conditions

Polarity, acid strength

Polarization lead-acid batteries

Primary Structure of Lipid A Backbone, Polar Substituents, and Fatty Acids

Sulfuric acid anodic polarization

Ursodeoxycholic acid polarity

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