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Problem Solving in General

The more complex a problem is, the less likely you will be able to see the answer from the start. Therefore you must begin work on the problem without any clear idea of how to work it. If so far you have always seen the answer from the start, working on a complex problem is, in a way, like flying on instruments through a cloud bank when you are used to visual navigation. Often students will just stare at the problem and wait for the answer to hit them. With difficult problems this can be a very long wait. These tips allow you to pursue the answer actively rather than waiting for it to come to you. [Pg.270]

Study with a pencil to underline important ideas make margin notes about things that do not make sense write down questions to ask the instructor make a written [Pg.270]

Collect a Toolbox of Commonly Needed Problem Solving Items [Pg.271]

As a start toward this, the Appendix gathers together important tools a p/fa chart, a bond-strength table, a list of sources and sinks, the electron flow pathways, trends, general rules, and other useful items. Continue to customize your toolbox with any valuable tools that you need. [Pg.271]

Be sure to know what is asked. Can you rephrase the question in your own words Make a model or draw a figure. Can you break the problem into separate, smaller, more easily solved units Can you give a rough estimate of the overall process  [Pg.271]


Source Ronald DeLorenzo, Problem Solving in General Chemistry, 2nd ed., Wm. C Brown, Publishers, Dubuque, Iowa, 1993, pages 336-338. [Pg.263]

Isoparametric mapping described in Section 1.7 for generating curved and distorted elements is not, in general, relevant to one-dimensional problems. However, the problem solved in this section provides a simple example for the illustration of important aspects of this procedure. Consider a master element as is shown in Figure 2.23. The shape functions associated with this element are... [Pg.51]

This problem is very difficult to solve in general however, we have to keep conditions (303) in mind, which we used in order to obtain the Fokker-Planck collision term (304). With this approximation, it is expected that the ions will exhibit random Brownian motion instead of free particle motion between two successive coulombic interactions. We shall thus refer to this model as the Brownian-static model (B.s.). [Pg.240]

To conclude, we venture to state that the problem of how to determine accurate optical constants from measurements on particulate samples, in contrast with homogeneous solids and liquids, has not been solved in general, even for single-component powders. This does not mean that there have not... [Pg.433]

Remark 3 The selection of a relaxation among a number of alternatives is based on the trade-off between two competing criteria. The first criterion corresponds to the capability of solving the relaxed problem easily. The second criterion is associated with the type and quality of lower bound that the relaxed problem produces for problem (P). In general, the easier the relaxed problem (RP) is to solve, the greater the gap is between the optimal solution of (P) and the lower bound provided by (RP). [Pg.99]

The calculation demonstrates that the concept of a strain-free bond has a clear electronic basis. It is important to note that in molecular mechanics the concepts of force constant and strain-free parameter are intimately linked. The calculated C-C pair, ke, do = (4.88 Ncm-1,1.51 A), are very close to the best empirically optimized values of the most extended force fields. Although special strategies will be required to calculate specific ke, do pairs, the problem may be considered solved in general and the empirical estimates used with confidence. As a rule of thumb it is noted that, to first approximation,... [Pg.227]

The question then becomes, which mechanism should we adopt to educate students properly in this area and thus overcome this deficiency There is no unique answer or magic formula. However, a good beginning is the intense practice of problem solving in specific areas of knowledge, although it would be desirable to have a more general syllabus of widespread applicability, at least in the hard core sciences. [Pg.3]

Any self-developed method or discipline will consist of personal features and individual points of view that may or may not reflect the opinion of the majority which may not necessarily be the most valid position. One should expect, therefore, that the criteria of those readers who have already created their own systematic approach to problem solving in mechanistic organic chemistry may be in conflict with some sensitive points expressed here. In addition, there are those who feel that rules in general jeopardize their ability to create and thus to find original solutions to problems. [Pg.176]

The actual reaction field can be computed with different PCM algorithms, which can be chosen according to the particular problem investigated in general, at each SCF cycle the solvation charges are determined by solving a linear system of the form... [Pg.499]

This is a modified version of the problem solved in section 17.10, though the boundary conditions are different. However, new aspects of the general problem of a transverse vibrating beam are considered here. [Pg.843]

On the other hand, tablet tooling design opens up for many possibilities for overcoming common tableting problems that cannot be solved by modifying the materials or the compression process, such as lubrication problems which in general are also a function of tooling size and shape. [Pg.3782]

One oil was inhomogeneous due to a high water content causing phase Separation. This may lead to erroneous results. The oil producer pointed out some problems during production, which now have been at least partly solved. In general, the accuracy of all physical analyses was good. Some results were systematically on high side, which most probably is due to poor calibration of the equipment. [Pg.1662]

Therefore, there exist two alternative possibilities. The first one is a positive sign of U oiRe), and the second one consists in a negative sign of U o(Re). Thus, the virial theorem does not exclude from the realm of possibilities the existence of more than one type of equilibrium position Re. The problem of the number of equilibrium positions has not yet been solved in general. [Pg.143]

For the majority of known liquids this has not hitherto been possible, e.g. it cannot be done with water. But since the problem has been solved for a number of liquids, we cannot doubt that it can be solved in general, either by discovering means of preventing crystallization by extremely rapid cooling or by examining suitable mixtures of liquids, or adsorbed liquids, and then extrapolating to the pure state. [Pg.99]


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