An alternative procedure

The need for lengthy calculations of the type just illustrated is avoided when tabulated values of AfH and AfG at various temperatures are available. Stull et al. [8] give this information for a large number of organic compounds and ref. 7 provides similar tables for many inorganic compounds. 

When Tables 4 and 6 are compared, it will be seen that AH values are almost the same by both methods, but there are small differences in the 

Tabulated values of standard enthalpies and free energies of formation [8] 

Enthalpy and Gibbs free energy changes and equilibrium constants for the reaction CO(g) + 2H2(g) = CHjOHCg) 

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An alternative procedure for the above test is as follows. Mix 2-3 ml. of 2 per cent, aqueous paraperiodic acid solution with 1 drop of dilute sulphuric acid (ca. 2 5N) and add 20-30 mg. of the compound. Shake the mixture for 5 minutes, and then pass sulphur dioxide through the solution until it acquires a pale yellow colour (to remove the excess of periodic acid and also iodic acid formed in the reaction). Add 1-2 ml. of Schiff s reagent (Section 111,70) the production of a violet colour constitutes a positive test. 

An alternative procedure is to leave the syrupy residue in a vacuum desiccator over anhydrous calcium chloride and siUca gel, and to Alter ofl the successive Crops of crystals as they separate. These are washed with light petroleum, b.p. 40-60°, spread on a porous tile and recrystallised. 

In an alternative procedure 26 g. of anhydrous ferric chloride replace the aluniiniuni chloride, the mixture is cooled to 10°, and the 50 g. of tert.-butyl chloride is added. The mixture is slowly warmed to 25° and maintained at this temperature until no more hydrogen chloride is evolved. The reaction mixture is then washed with dilute hydrochloric acid and with water, dried and fractionally distilled. The yield of tert.-butyl benzene, b.p. 167- 170°, is 60 g. 

I) An alternative procedure is to cool the solution containing the sodium sul. phanilate and sodium nitrite in a bath of crushed ice to about 5° and then add 10-5 ml. of concentrated hydrochloric acid diluted with an equal volume of water slowly and with stirring the temperature must not be allowed to rise above 10 and an excess of nitrous acid should be present (the solution is tested after standing for 5 minutes). The subsequent stages in the preparation—addition of dimethyl-aniline solution, etc.—are as above. 

An alternative procedure, more suitable for the preparation of somewhat larger quantities of the bromo derivative, is the following. Dissolve 10 g, of the compovmd in 10-15 ml. of glacial acetic acid, cautiously add 3-4 ml. of hquid bromine, and allow the mixture to stand for 15-20 minutes. Pour into 50-100 ml. of water, filter off the bromo compound at the pump, and wash with a httle cold water. Recrystallise from dilute alcohol. 

An alternative procedure, which does not require ice cooling, is to add all the 10 ml. of benzoyl chloride rapidly to a mixture of 50 ml. of concentrated ammonia solution and 60 ml. of water contained in a 200 ml. conical flask, stopper securely and shake vigorously for about 15 minutes. Heat is evolved So that the stopper should be held down tightly. After 30 minutes the benzamide is filtered off and worked up as above. 

The determination of the saponification equivalent of an ester by the alcohohc potassium hydroxide method is described in Section 111,106 an alternative procedure using diethylene glycol is given below. This constant should be determined if possible in the prehminary examination, since a knowledge of its value together with the boihng point provides a basis for a fairly good approximation of the size of the ester molecule. 

An alternative procedure involves use of alkyl nitrites and traps the desired product as an acetal[16],... 

Castillo, C. A. Jaramillo, A. An Alternative Procedure for Titration Curves of a Mixture of Acids of Different Strengths, /. Chem. Educ. 1989, 66, 341. 

In an alternative procedure the acids themselves undergo cyclization cataly2ed by hydrogen fluoride. y-Phenylbutyric acid [36541-31-8] can be cychzed to a-tetralone [29059-07-2] by this method ... 

Moderate yields of acids and ketones can be obtained by paHadium-cataly2ed carbonylation of boronic acids and by carbonylation cross-coupling reactions (272,320,321). In an alternative procedure for the carbonylation reaction, potassium trialkylborohydride ia the presence of a catalytic amount of the free borane is utilized (322). FiaaHy, various tertiary alcohols including hindered and polycycHc stmctures become readily available by oxidation of the organoborane iatermediate produced after migration of three alkyl groups (312,313,323). 

In an alternative procedure (84), the electrolyte is pumped through the cells at such a rate that the outlet concentration is 50 g/L MnSO and 67 g/L H2SO4. This spent electrolyte is then mixed with equal parts of make-up solution containing 150 g/L MnSO and the mixture returned to the electrolysis step. The electrolysis is continued over a period of days and terrninated when the EMD layer deposited on the anode reaches a specific thickness, usually on the order of 1—3 or 6—8 mm. Following completion of the electrolysis cycle, the entire electrode assembly is removed from the cell for removal of the deposited EMD, either manually or by an automated system (85). The product is repeatedly washed with water to extract the occluded acid (83) and dried at about 85°C in air. 

An alternative procedure for the preparation of (R)-calcium pantothenate (3) is to condense (R)-pantolactone (9) with the preformed calcium salt (12) of p-alaniue (15). 

Chloroform may be estimated quantitatively by determining the amount of copper oxide produced when it is warmed with Fehling s solution, which is potassium cupritartrate (34). An alternative procedure consists of heating the chloroform with concentrated alcohoHc potassium hydroxide in a sealed tube at 100°C and determining the amount of potassium chloride produced (35). 

Confirmation of the formation of the radicals during combustion reactions has been made by inuoducing a sample of dre flames into a mass spectrometer. The sample is withdrawn from a turbulent flame which is formed into a thin column, by admitting a sample of the flame to the spectrometer drrough a piidrole orifice, usually of diameter a few tenths of a millimetre. An alternative procedure which has been successful in identifying the presence of radicals, such as CHO, has been the use of laser-induced fluorescence. 

For shorter penetration the use of p emitting isotopes is widely made applying much the same absorption law for p radiation as for y rays, with a minor modification. An alternative procedure used by Kingety and Paladino for the study of diffusion in AI2O3 employs two right cylinders, one only containing the radioactive Al isotopic species which emits relatively low energy ( ,nax = 0.511 MeV) p particles. 

An alternative procedure used for large apparatus is to rinse the apparatus with a 5% solution of dichloromethyl silane in chloroform, followed by several rinses with water before baking the apparatus at 180°/2h (for glass) or drying in air (for plasticware). 

An alternative procedure rescales the coordinates of each atom at each time step [24]. The atomic coordinate x and the characteristic distance for repeating boundary conditions, d, are rescaled to values uc and fid, respectively, where... 

Iron pentacarbonyl and l-methoxy-l,4-cyclohexadiene react as shown by Birch and oo-workera, but in dibutyl ether this solvent has been found superior. The tricarbonyl(methoxy-l,3-cyclohexadiene)iron isomers undergo hydride abstraction with triphenylmethyl tetrafluoro-borate to form the dienyl salt mixture of which the 1-methoxy isomer is hydrolyzed by water to the cyclohexadienone complex. The 2-methoxy isomer can be recovered by precipitation as the hexafluoro-phosphate salt. By this method the 3-methyl-substituted dienone complex has also been prepared from l-methoxy-3-methylbenzene. The use of the conjugated 1-methoxy-1,3-cyclohexadiene in Part B led to no increase in yield or rate and resulted chiefly in another product of higher molecular weight. An alternative procedure for the dienone is to react tricarbonyl(l,4-dimethoxycyclohexadiene)iron with sulfuric acid. ... 

An alternative procedure is the dynamic programming method of Bellman (1957) which is based on the principle of optimality and the imbedding approach. The principle of optimality yields the Hamilton-Jacobi partial differential equation, whose solution results in an optimal control policy. Euler-Lagrange and Pontrya-gin s equations are applicable to systems with non-linear, time-varying state equations and non-quadratic, time varying performance criteria. The Hamilton-Jacobi equation is usually solved for the important and special case of the linear time-invariant plant with quadratic performance criterion (called the performance index), which takes the form of the matrix Riccati (1724) equation. This produces an optimal control law as a linear function of the state vector components which is always stable, providing the system is controllable. 

Deuterium labeling of C-18 has also been accomplished by an alternate procedure adapted from the Nagata steroid synthesis. During the course of the total synthesis of pregnanolone, thevC-18 function is introduced in the form of a nitrile group. Reduction of this function in intermediate (247) with lithium aluminum deuteride leads to a deuterated imine (248), which upon Wolff-Kishner reduction and acid-catalyzed hydrolysis... 

Note 1. An alternative procedure proceeds by oxidation of the 3/5-hydroxy group with chromic acid-sulfuric acid and subsequent elimination of hydrogen chloride by treatment of the intermediate chloroketone with potassium acetate in methanol. Good overall yields are obtained with this reaction sequence in the androstane series. 

The equivalency of sites required for the application of these equations is seldom found in practice, although many authors apply these corrections. Benson has described an alternative procedure in which the rate and equilibrium constants are... 

Ashland admitted that Uie usual testing procedures were not employed before putting tlie tank into service. Hydrostatic testing is recommended by the American Petroleum Institute, but pumps large enough to gel water to the lop of tlie lank were not tnailable at the site. An alternate procedure was performed in which the lank was sprayed with diesel fuel and subjected to a vacuum. However, the lank was not inspected by any outside agency prior to use. 

Quinazoline hydroxamic acids (26) can be prepared by acylation of an o-aminobenzohydroxamic acid (25). An alternative procedure... 

An alternate procedure has recently been described (5). In a 100-ml flask equipped with a condenser and a magnetic stirrer, 10 g of 1-bromoadamantane is mixed with 15 ml of 0.67 N hydrochloric acid and 13 ml of DMF. The mixture is heated at 105° for... 

An alternate procedure is to calculate (1) the pressure drop series-wise one section of the line at a time, or (2) capacity for a fixed inlet pressure, series-wise. 

An alternative procedure is the reverse-bend test in which the specimen in the form of wire or strip is bent repeatedly backwards and forwards over a mandrel until it fractures, the number of bends indicating the degree of embrittlement. However, this method is considered to be less sensitive than the single-bend test. 

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