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(9101) This step, yielding a cisoid ~-hydroxyethylpalladium intermediate (71), is preceded by a trans-cis isomerization (69 to 70)498 A series of hydride shifts (66 to 67 and 67 to 68) eventually leads to the product carbonyl compound Of the other olefins, short-chain terminal alkenes are oxidized to methyl ketones Propylene gives predominantly acetone with a negligible amount of propionaldehyde I-Butene and 2-butenes are converted to 2-butanone in about 90% yield The rate of oxidation decreases in the order ethylene> propylene> butenes, which is consistent with the nucleophilic attack on the coordinated alkene Higher homologs are oxidized very slowly and afford some chlorinated products and a mixture of isomeric ketones resulting from the palladium-catalyzed isomerization of the alkene facilitated by high temperature Cyclodextrins, however, used in a two-phase system greatly improve the yields and selectivities of the oxidation of C8-C IO alkenes.

InDesign s Edit menu (shown in Figure 2.32) provides access to its invaluable multiple undo and redo features, as well as the standard Cut, Copy, Paste, and Clear commands. You ll find Duplicate, and Step and Repeat here, even though you might be searching the Object menu for them. The Edit menu also provides commands for searching and replacing text and formats, checking spelling, and editing spelling and hyphenation dictionaries, as well as for opening the Story Editor text-editing feature and setting up stories for the InCopy add-on program. It also provides access to color settings and keyboard shortcut preferences. The Windows version also contains the Preferences menu option (which is in the InDesign menu on the Mac). Note that these menu items functions, except for Quick Apply, are not available in panels.

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Class A single CSS class. Tag A single HTML tag. Advanced Any type of selector other than single classes or single tags. This category includes IDs, contextual selectors, grouped selectors, pseudo-classes, pseudo-elements, as well as universal, child, adjacent-sibling, or attribute selectors.

2. Open the Behaviors panel by choosing Window Behaviors or by pressing Shift+F3. 3. Click the Add (+) button to reveal the available options, as shown in Figure 12-2. Select one from the drop-down list. 4. Enter the desired values in the action s parameter dialog box. 5. Click OK to close the dialog box when you re finished. Dreamweaver adds a line to the Behaviors panel displaying the attached event and its associated action.

< xml version= 1.0 encoding= utf-8 > <s:Application xmlns:fx= http://ns.adobe.com/mxml/2009 xmlns:s= library://ns.adobe.com/flex/spark xmlns:mx= library://ns.adobe.com/flex/mx > <s:layout> <s:VerticalLayout horizontalAlign= center paddingTop= 20 gap= 20 /> </s:layout> <s:RichText id= myRichText > <s:content> <s:p fontSize= 10 fontFamily= _sans > A small normal paragraph in a serif font</s:p> <s:p fontSize= 14 fontWeight= bold fontFamily= _serif > A medium bold paragraph in a sans serif font</s:p> <s:p fontSize= 18 fontFamily= _typewriter >A large <s:span fontStyle= italic >mixed-text</s:span> paragraph in a typewriter font</s:p> </s:content> </s:RichText> </s:Application>

511 The (RCNhPdCI 2 complex in the presence of CuCI, a chloride salt in tert-BuOH was shown to exhibit unusually high selectivity for aldehyde formation (up to 57%)512 An important drawback of the original Wacker process is the highly corrosive nature of the aqueous acidic PdCI 2-CuCI2 system Attempts were made to apply electrochemical reoxidation of palladium,513,514 and to use other oxidants,495 such as Fe(III) salts, Mn02, quinones,514-516 peroxides,517,518 and more recently, heteropoly acids 516 ,519-522 Successful modifications to improve the oxidation of nonterminal alkenes include the use of organic solvents Oxidation in anhydrous 523 ,524 or aqueous alcohols,525 N,N-dimethylformamide,526 and sulfolane527 may convert internal alkenes and cycloalkenes into ketones in high yields with high selectivities Cyclohexene, for example, is transformed to cyclohexanone in 95% yield (ethanol, 90 C, 2 h).

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After you ve corrected the problem, the red underline is removed. You can verify your change has eliminated the error by using any of the methods described in the following steps: 1. Open the Browser Check menu and choose Check Browser Support or choose File Check Page Check Target Browsers. Dreamweaver checks the page and lists the results in the Target Browser Check panel, as shown in Figure 29-7. This is a very handy debugging tool. For each error found, the filename, line number, and a short description are listed. Double-clicking on an item in the list displays the offending code in Code view, highlighted and ready to be debugged. Dreamweaver displays the results temporarily and deletes them when you check another page or close the program. 2. To display a report of these results in your primary browser (see Figure 29-8), click the Browse Report button.

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