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Solutions observing

Now warm 2-3 drops of acetaldehyde with 3-4 ml. of 10-20 per cent, sodium hydroxide solution, i.e., with excess of concentrated alkali solution. Observe the formation of a yellow aldehyde resin and the attendant peculiar odour. [Pg.331]

Ferric chloride test. Dissolve 1 drop or 0 05 g. of the compound in 5 ml. of water and add 1 drop of ferric chloride solution observe the colour produced. If the result is negative in aqueous solution, repeat the test in alcoholic solution. [Pg.1072]

Figure 8.1 Effect of pH on corrosion of 1100-H14 alloy (aluminum) by various chemical solutions. Observe the minimal corrosion in the pH range of 4-9. The low corrosion rates in acetic acid, nitric acid, and ammonium hydroxide demonstrate that the nature of the individual ions in solution is more important than the degree of acidity or alkalinity. (Courtesy of Alcoa Laboratories from Aluminum Properties and Physical Metallurgy, ed. John E. Hatch, American Society for Metals, Metals Park, Ohio, 1984, Figure 19, page 295.)... Figure 8.1 Effect of pH on corrosion of 1100-H14 alloy (aluminum) by various chemical solutions. Observe the minimal corrosion in the pH range of 4-9. The low corrosion rates in acetic acid, nitric acid, and ammonium hydroxide demonstrate that the nature of the individual ions in solution is more important than the degree of acidity or alkalinity. (Courtesy of Alcoa Laboratories from Aluminum Properties and Physical Metallurgy, ed. John E. Hatch, American Society for Metals, Metals Park, Ohio, 1984, Figure 19, page 295.)...
Fig. 2. a) Transient absorption spectra of RF (35 pM) in N2-saturated MeOH-Water (1 1) solution observed after 60 ps of the laser pulse as a function of the concentration of GA. b) Effect of dissolved molecular oxygen ( 2) on the decay of the 3RF at 700 nm. Inset Stern-Volmer plot for the quenching of 3RF by 3O2. [Pg.14]

To the first test tube, add 1 mL of 0.1M potassium thiocyanate solution. Observe and record the color change in Data Table 1. [Pg.138]

The reduction electrochemistry of ECP porphyrin films furthermore responds to added axial ligands in the expected ways. We have tested this (2,6) for the ECP form of the iron complex of tetra(o-amino)phenyl)porphyrin by adding chloride and various nitrogeneous bases to the contacting solutions, observing the Fe(III/II) wave shift to expected potentials based on the monomer behavior in solution. This is additional evidence that the essential porphyrin structure is preserved during the oxidation of the monomer and its incorporation into a polymeric film. [Pg.412]

The solid solution observed between silane and germane and the very close X-ray powder diffraction of both compounds are the evidence of isostery, i.e. of the same structure. [Pg.162]

Rinse the beaker thoroughly, then add 25 mL distilled water and a drop of phenolphthalein solution. Use forceps to place a small piece of CaC2 in the solution. Observe the results. [Pg.85]

The lattice models provide useful interpretations of spin relaxation in dissolved polymers and rubbery or amorphous bulk polymers. Very large data bases are required to distinguish the interpretive ability of lattice models from other models, but as yet no important distinction between the lattice models is apparent. In solution, the spectral density at several frequencies can be determined by observing both carbon-13 and proton relaxation processes. However, all the frequencies are rather hl unless T2 data are also included which then involves the prospect of systematic errors. It should be mentioned that only effective rotational motions of either very local or very long range nature are required to account for solution observations. The local... [Pg.284]

This is not the only subject of debate the nature of the adsorbed forms of oxygen and reaction products on the electrode surface has been widely discussed, as well as the various steps of ORR. Very often, for conditions apparently similar, for example, the same electrode and solution, observations made by two research groups are different and so are, of course, the deductions and the pathways for the electrode reaction. There are so many possible steps, reactions and species that various combinations can be envisaged moreover, as other methods for observing the species or intermediates involved in the electrode reaction are rare, electrochemistry is often the only source of experimental facts. As for other multiparametric problems, when a plausible explanation is found, there is no certainty that this is the only possibility and the correct solution. Moreover, experimental conditions that look identical are not really exactly similar the problem... [Pg.129]

Coherent nuclear motion of reacting excited-state molecules in solution observed by ultrafast two color pump-probe spectroscopy... [Pg.295]

The transition from a stable steady-state solution observed at large p to the oscillatory regime assumes the existence of the critical value of the parameter pc, which defines the point of the kinetic phase transition as p > pc, the fluctuations of the order parameter are suppressed and the standard chemical kinetics (the mean-field theory) could be safely used. However, if p < pc, these fluctuations are very large and begin to dominate the process. Strictly speaking, the region p pc at p > pc is also fluctuation-controlled one since here the fluctuations of the order parameter are abnormally high. [Pg.48]

The teacher should dissolve 10.0 g of CuS04 in 90.0 g of distilled water, H20 (1.0 ml H20 = 1.0 g). This results in a 10% solution of CuS04. Calculate the mass percent of this solution (mass of solute in grams, 10.0, divided by mass of solution in grams, 10.0/100.0 =. 100, multiplied by 100 to find percent) to verify that it is a 10% solution. Observe the color. [Pg.54]

Solution Observation with 0.5 M AgN03 Color in Flame Test... [Pg.55]

All solutions should be placed in dropper bottles. In preparing all acid and base solutions, observe personal safety practices. Use a face shield, rubber gloves, and a rubber apron. Do preparations in the hood. [Pg.540]

To the remainder of the solution add 5 cc. potassium permanganate solution. Observations Equations Filter to the colorless filtrate add 5 cc. barium chloride solution. Let settle, pour off the supernatent liquid, add 5 cc. 12 N hydrochloric acid to the residue and boil for 2 minutes. Dilute to 25 cc. Add 1 to... [Pg.336]

Avdeef (2001) described the influence of membrane retention of solutes observed in PAMPA experiments on the data evaluation. Membrane retention is analysed using a mass balance between compound left in donor compartment after incubation and compound determined in acceptor compartment after incubation. For calculating Papp under consideration of membrane bound fraction Avdeef (2001) used a equation different from equation (2) where the total amount of solute is substituted by the non-membrane bound fraction of solute in the equation. [Pg.470]

The nineteenth century also produced reagents for the one-electron oxidation of suitable substrates. For example, sulfuric acid was employed for many years as an analytical reagent because of some color reactions. Thus, Laurent treated benzimid , C28H10O2+HAz, a residue from the oil of bitter almonds (ben-zaldehyde) and observed an indigo blue solution [34]. On the other hand, the blue solution observed by Liebermann upon treatment of chrysene with sulfuric acid can be attributed to the chrysene radical cation [43]. [Pg.8]

Fig. 6. Liquid crystals of Pt-D -Pd-D1 polymer in a trichloroethylene solution observed between crossed polarizers at about 200X (left) droplets of a liquid-crystalline phase in the dark background of the isotropic phase (right) thin layer of a large liquid-crystalline phase... Fig. 6. Liquid crystals of Pt-D -Pd-D1 polymer in a trichloroethylene solution observed between crossed polarizers at about 200X (left) droplets of a liquid-crystalline phase in the dark background of the isotropic phase (right) thin layer of a large liquid-crystalline phase...
Transfer to 2 test-tubes either 1-ml portions of filtered or clarified gastric contents, or 5-ml portions of stomach washings. To one tube add an equal volume of silver nitrate solution, observe the reaction and dien add a 30% v/v solution of nitric acid. To the second tube add an equal volume of barium chloride solution, observe die reaction and then add a 30% solution of nitric acid. [Pg.64]


See other pages where Solutions observing is mentioned: [Pg.376]    [Pg.120]    [Pg.376]    [Pg.250]    [Pg.6]    [Pg.80]    [Pg.356]    [Pg.376]    [Pg.335]    [Pg.155]    [Pg.356]    [Pg.32]    [Pg.347]    [Pg.104]    [Pg.54]    [Pg.54]    [Pg.159]    [Pg.201]    [Pg.215]    [Pg.399]    [Pg.170]    [Pg.173]    [Pg.187]    [Pg.493]    [Pg.220]   
See also in sourсe #XX -- [ Pg.383 ]




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