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There are 71,376 orders in New York and California, with an average order size of $73.98 and a standard deviation of $197.23. The orders from California are a subgroup of this population, comprising 17,839 orders with an average order size of $85.48. What is the confidence that this subgroup is just a random sample pulled from the data (meaning that the observed difference is due only to chance) As mentioned earlier, the standard deviation of the sample average is the standard deviation of the overall data divided by the square root of the sample size. For instance, the 17,839 orders from California constitute a sample from the original population. Based on the overall data the average expected value should be $73.98 and the standard deviation $197.23 divided by the square root of 17,839, which is about $1.48.

Edward R. Tufte, author of several books that deal with the visual presentation of data, refers to the principle of data ink maximization. Simply put, this principle states that the most effective charts use their ink to display data not chart accoutrements such as grid lines and labels. Consequently, nonessential chart elements can often be deleted with little or no adverse effect on the readability of the chart. Figure 11-19 shows a typical column chart on the left and a minimalist version of the chart on the right. There s certainly nothing wrong with the original version of this chart. The chart on the right, however, removes all nonessential elements and the basic message remains. The chart on the right underwent the following modifications:

Even if you are not planning on setting up an audio recording studio, it's helpful to understand the basic computer

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1. Choose File New Document or press +N or Ctrl+N. 2. Select the Master Text Frame option at the top of the New Document dialog box.

Using the Hidden Field and the File Field The hidden input type . . . . . . . The file input type . . . . . . . . . Improving Accessibility . . . . . . . . . . Styling Forms with CSS . . . . . . . . . . Encompassing the form . . . . . . Altering input fields . . . . . . . . Distinguishing lists and menus . . Changing labels and legends . . . Highlighting focus . . . . . . . . . Summary . . . . . . . . . . . . . . . . . .

7

In the case of the standard Google Maps interface you also obtain two Directions links ( To here and From here ) that provide an interface to the Google route-finding service, which calculates, highlights, and describes a route between two points. Figure 2-17 shows a route from a railway station to a restaurant.

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Here s how to get real square corners:

Coupling of monosaccharides requires activation of the anomeric position in one monosaccharide (electrophilic acceptor or glycosyl donor) and protection of all functional hydroxyl group positions except for the selected hydroxyl group in the other monosaccharide (nucleophilic donor or glycosyl acceptor). The very simplest form of this is illustrated (Figure 2.13). Initially, protecting group manipulation is required, followed by coupling, which should be as stereocontrolled as possible. Protecting groups are chosen to assist in the current glycosidic link formation but also with an eye to subsequent glycosidic link formations. Making the right choices of protecting groups and coupling reagents is essentially an empirical exercise based upon a detailed knowledge of oligo-/polysaccharide chemistry. In other words, what will and will not work is still effectively the preserve of an initiated few who possess detailed experience. In recent times, the following synthetic methodologies have emerged as leading ways to effect glycosidic link formation: (a) glycosyl trichloroacetamidate coupling (b) 1,2 anhydrosugar-thioglycoside coupling (c) n-pentenyl glycoside coupling. The rst (a) has been extremely useful in many solution phase oligo-/polysaccharide syntheses. Glycosyl donors (electrophilic acceptors) are activated under very mild conditions by catalytic amounts of trimethylsilyltri ate (TMSOTf) and other tri ates including dibutyl boron tri ate (DBBOTf), not to mention boron tri uoride in diethylether (BF3 /Et2 O). This method of glycosidic link formation is striking for control of the stereochemistry ( or ) of the anomeric centre and hence of the glycosidic link (Figure 2.13). The second method (b) involves 1,2-anhydrosugars that are obtained easily from glycal precursors. Glycals are readily converted into corresponding anhydrosugars by epoxidation with dimethyl

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