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In ordinary Java programming, when a class does too much, you want to refactor it into smaller objects that collaborate to achieve the same result in a more flexible way. The hope is that you can then use the components in other applications as well. In this section we'll introduce you to three ways to add functionality when dealing with servlets. This means that when you need to split up responsibility, you can reach for the appropriate technique. In addition, a servlet is running within a JVM so it has access to your usual bag of tricks. Here you'll see how to create filters that work with the request before it gets to the servlet and then alter the response once it leaves. We'll also discuss forwarding the results of one servlet to another resource. Finally, we'll show you how to use an include() method to combine the output of two servlets.

12: Parsing Documents with JAXP The following example shows one way you might modify your running example to output the number of lines for a given character in Richard III. You'll need to keep track of when the given character is speaking. Whenever a new speech begins, reset the boolean mySpeech to false. Then check the character data: If it matches up with the name of the character in the play, set mySpeech to false. If the element is a LINE, increment the totalLineCount as before. If mySpeech is true, increment characterLineCount as well. This process only sounds complicated because we are using character to mean the role played in Richard III as well as a char being parsed by your SAX parser. Here's CueMyLine2.java with the changes highlighted:

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randomness and utter chaos may be all there is to it We seek the comfort of order and con ourselves into believing that someone, somewhere must have the answers, down to the third decimal We don t want to walk the nancial street alone; we seek expert guidance Thus are born the professions of market analyst, rating agent, nancial reporter, and, naturally, nance theoretician These people exist out of our need to have our hands held, to be cuddled and sung comforting lullabies amidst the vast unknown We need to be told whether we should buy or sell, whether the stock price will be $457 or $473, whether the structured credit vehicle is AAA trustworthy or BB crap, and whether expected volatility is 30 percent or 40 percent Yes, yes, deep inside we may be fully aware of the utterly blatant inaccuracies that such statements typically contain.

Ultraviolet, visible, and near-infrared spectra of metal coordination and organometallic polymers can be helpful in substantiating the arrangement of ligands about metal ions with partially lled d orbitals, the oxidation state of the metal ions, etc The d-d, charge-transfer (also called electron-transfer), and intervalence charge-transfer transitions (cf Fig 336) typically occur in one or more of these spectral regions as detailed in almost all inorganic chemistry textbooks above the general chemistry level A recent two-volume work (58) has a great deal of information on the electronic spectroscopy of metal coordination compounds including chapters on polarized absorption spectroscopy, luminescence spectroscopy, and laser spectroscopy that are not covered here More detailed information on electronic spectra through ligand eld theory was published recently by Figgis and Hitchman (59) and earlier by Lever (60, 61), Figgis (62), J rgensen (63, 64), Ballhausen (65), and others.

After all, how many times do analysts get the call wrong How many times did the stock drop when it was supposed to rise How many times did the AAA paper end up worthless How many times did risk underestimate true danger How many times did uncorrelated assets tank together And yet, even for those slightly savvier, self-enslavement to perceived expertise runs rampant, an incurable addiction We never cease to unremittingly require our regular x of precision-promising exactness Interestingly enough, our unconditional servitude may be most unfettered in the case where the promise of darkness-combating may be least ful lled It is undeniable that analysts and rating agencies have proven less than reliable on many occasions, and we wouldn t deserve the lunatic label for af rming that both have behaved in inadmissibly fraudulent ways in the past.

Metal-containing inorganic polymers are often characterized by their electronic spectra and by their d-d spectra in particular Examples of d-d spectra for nickel(II) coordination species in solution with various geometrical arrangements are shown in Figures 337 and 338 Note that the molar extinction coef cients ( ) for the d-d transitions of octahedral nickel(II) complexes (Fig 337a) are normally less than 10 M 1 cm 1 whereas the values for the other geometries (Figs 337b and 338) are typically quite a bit higher All true d-d transitions are symmetry forbidden with low intensities and except for their vibronic coupling, they would have no intensity at all fVibronic coupling implies a vibration of the same symmetry as the electronic transition coupling with the electronic transition.

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