Water experimental procedures

Gum arable, CoCb 6 H2O, cooking salt, water-insoluble dyes, distilled water. Experimental Procedure... 

Unfortunately, in most cases not all the available information on a reaction is given in the reaction equation in a publication, and even less so in reaction databases. To obtain a fuller picture of the reaction that was performed, the text describing the experimental procedure in the publication or a lab journal) would have to be consulted. Reaction products that are considered as trivial, such as water, alcohol, ammonia, nitrogen, etc., are generally not included in the reaction equation or mentioned in the text describing the experimental work. This poses serious problems for the automatic identification of the reaction center. It is highly desirable to have the full stoichiometry of a reaction specified in the equation. 

The experimental procedure to be followed depends upon the products of hydrolysis. If the alcohol and aldehyde are both soluble in water, the reaction product is divided into two parts. One portion is used for the characterisation of the aldehyde by the preparation of a suitable derivative e.g., the 2 4-dinitrophenylhydrazone, semicarbazone or di-medone compound—see Sections 111,70 and 111,74). The other portion is employed for the preparation of a 3 5-dinitrobenzoate, etc. (see Section 111,27) it is advisable first to concentrate the alcohol by dis tillation or to attempt to salt out the alcohol by the addition of solid potassium carbonate. If one of the hydrolysis products is insoluble in the reaction mixture, it is separated and characterised. If both the aldehyde and the alcohol are insoluble, they are removed from the aqueous layer separation is generally most simply effected with sodium bisulphite solution (compare Section Ill,74),but fractional distillation may sometimes be employed. 

Many reagents are able to chlorinate aromatic pyrazole derivatives chlorine-water, chlorine in carbon tetrachloride, hypochlorous acid, chlorine in acetic acid (one of the best experimental procedures), hydrochloric acid and hydrogen peroxide in acetic acid, sulfuryl chloride (another useful procedure), etc. iV-Unsubstituted pyrazoles are often used as silver salts. When methyl groups are present they are sometimes chlorinated yielding CCI3 groups. Formation of dimers and trimers (308 R = C1) has also been observed. 

A solution of estradiol (38, 15 mg) in methanol-OD (4 ml) and one drop of 10% deuteriosulfuric acid in deuterium oxide is heated under reflux for 5 days. After cooling the reaction mixture is diluted with ether, washed with dilute sodium bicarbonate solution and water, then dried over anhydrous sodium sulfate. Evaporation of the ether gives crystalline 2,4-d2-estradiol (39, 15 mg, 99%), mp 173-175° (ether-hexane), exhibiting 82% isotopic purity and only one aromatic hydrogen by NMR. (For an experimental procedure describing the exchange of aromatic protons under Clemmensen conditions, see section III-D.)... 

This chapter describes the use of three commercially available SEC column types for the characterization of nonionic, anionic, and cationic, synthetic water-soluble polymers. These include TSK-PW, Synchropak, and CATSEC columns. Specific examples and experimental procedures are discussed for each type of column. Elowever, the major emphasis is on the use of TSK-PW columns due to their broad applicability for a variety of water-soluble polymers. 

At present, it is reported that there is no analytical technique capable of quantifying the entire organotin compound with its associated ligand in dilute solutions in water (Parametrix, 2002g), although experimental procedures are under development that may allow for determination of the entire organotin compormd in water (e.g. Yoder, 2003). 

For desymmetrization of diesters 3 via their hydrolysis in water, pig Hver esterase [12], o -chymotrypsin [12, 13a], and Candida antarctica Hpase (CAL-B) [14] were successfully used. However, further studies showed that respective anhydrides 5 can be used as substrates for enzyme-catalyzed desymmetrization in organic solvents [15]. The desired monoesters 4 were obtained in high yield in this way, using immobilized enzymes Novozym 435 or Chirazyme L-2 (Scheme 5.3). After the reaction, enzymes were filtered off, organic solvents were evaporated, and the crude products were crystalHzed. This was a much simpler experimental procedure in which control of the reaction progress was not necessary, and aU problems associated with extraction of products from aqueous phase and their further purification were omitted [15]. 

Experimental conditions are listed in Table 2. After pyrolysis of samples at 1073K, the product char was washed with pure water and chlorine of the leachates was analyzed by ion chromatography. Refer to the reference [3] for a detailed experimental procedure. 

The general experimental procedure employed in the study here has been described previously (7), thus only a brief overview is presented here. For all experiments, 45 mL deionized water and catalyst (50 mg Pd-black for 3-buten-2-ol and 25 mg for l,4-pentadien-3-ol) were added to the reaction cell. For ultrasound-assisted, as well as stirred (blank) experiments, the catalyst was reduced with hydrogen (6.8 atm) in water for 5 minutes at an average power of 360 W (electrical 90% amplitude). The reagents (320 mg 3-buten-2-ol or 360 mg l,4-pentadien-3-ol) were added to the reduced catalyst solution to achieve... 

Winge et al. [730] have investigated the determination of twenty or more trace elements in saline waters by the inductively coupled plasma technique. They give details of experimental procedures, detection limits, and precision and accuracy data. The technique when applied directly to the sample is not sufficiently sensitive for the determination of many of the elements at the low concentrations at which they occur in seawater, and for these samples preconcentration techniques are required. However, it has the advantages of being amenable to automation and capable of analyzing several elements simultaneously. 

Bjerre, H.L., T. Hvitved-Jacobsen, B. Teichgraber, and D. te Heesen (1995), Experimental procedures characterizing transformations of wastewater organic matter in the Emscher river, Germany, Water Sci. Tech., 31(7), 201-212. 

In other words even with the most rigorous experimental procedure the amount of residual water could not be reduced significantly below [H2()]f at temperatures below -60°, so that in that temperature range only comparatively few incomplete reactions were achieved. Reactions which had stopped by consumption of water could always be re-started by the admission of moist air or the breaking of a phial containing water. It was found that at -60° the yield obeyed the relation... 

As an example of a partition coefficient, the octanol-water partition coefficient (K0Vf) is determined by similar experimental procedures as those for... 

One variation to the usual experimental procedure was tried. In this test, liquid ethane was impacted on a 293-K water surface. This was accomplished by evacuating the air space between the water container and an ethane reservoir above. When the ethane reservoir was broken by... 

The experimental procedure below describes the uptake of ciprofloxacin into sphingomyelin (SPM)/Chol LUVs. Drug delivery vehicles prepared from SPM/Chol often exhibit greater efficacy than those prepared from DSPC/Chol (13). Included is a description of the Bligh-Dyer extraction procedure (78), which involves partitioning the lipid and water-soluble drug into organic solvent and aqueous layers, respectively. This is necessary because lipid interferes with the ciprofloxacin assay. 

The carbonium ion formed in equation 129 would be able, to start a new chain and each water molecule would thus cause the formation of more than one polymer molecule. If, on the other hand, the possibility of this chain transfer is excluded, and if it is assumed that only activated TiCl4 H20 molecules can act as initiators, each water molecule will give rise to only one polymer molecule. The experimental data showed that the molar quantity of water added to initiate the reaction was of the same order as the number of molecules formed, but it does not seem probable, considering the experimental procedure, that each water molecule could enter into reaction. 

The technical production of poly(benzimidazole) (PBI) is also carried out in two steps. In the first step an aromatic tetramine is condensed with the diphenyl ester of an aromatic dicarboxylic acid at 220-260 °C, yielding a poly(amino amid) with elimination of phenol. Ring closure with elimination of water occurs in the second step (solid-phase polycyclocondensation), conducted at 400 °C and yielding the polybenzimidazole (experimental procedure, see Table 2.3). 

However, the experimental procedure that was applied had to be slightly different, as it is not easy to build a surfactant starting from two water-soluble moieties. Rather, one of the two should be lipophylic, as shown in the Figure 7.14. 

AND EXPLOSION), EXPERIMENTAL PROCEDURES . Determination of shock pressure required to initiate detonation of an acceptor in the shock sensitivity test is described in Ref 8 Refs 1) W.C. Holton, "The Detonation Pressure in Explosives as Measured by Transmitted Shocks in Water , NavOrdRept 3968(1954) (Conf) 2) Dunkle s Syllabus (1957-1958), p 175 3) Cook (1958), 68-9... 

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