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Like SFIR, reduced susceptibility to multipath effects can be achieved by exploiting spatial filtering properties. In this case spatial filtering reduces the channel s delay spread. This is because signals arriving at angles outside of the main beam will be attenuated. These signals will have longer path lengths and would normally contribute to the longer delays of the channel impulse response. The consequence of reducing delay spread is that equalisation techniques are no

CrossReference See the section, Attaching a material to a face in 24 for information on how to attach a material to the face of a solid using the SOLIDEDIT command.

where L is a linear operator and where y can represent a vector or a function that is subject to certain boundary conditions. When y is a vector, L represents a matrix and y is termed an eigenvector. In linear algebra, a scalar is called an eigenvalue of a linear mapping L if there exists a nonzero vector y such that Ly y. The vector y is called an eigenvector. When y is a function, L can represent a di erential or integral form, in which case y is called an eigenfunction.

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data is not sent to the server. Sometimes the field is sent as an empty string; sometimes no field name is sent at all. The following table illustrates the behavior of various form controls when they re not filled in or selected:

Before you install, make sure that your system meets the minimum, and preferably the recommended, requirements: Operating system: Windows 2000, Windows XP (Home, Professional, or Tablet PC) Processor: Pentium III or better, 800 MHz minimum RAM (memory): 512MB (recommended) Video: 1024 768 VGA with true color; optional Open GLcompatible 3D video card with an OpenGL Installable Client Driver (ICD) Hard disk: 500MB for installation (300MB for AutoCAD LT) Pointing device: Mouse, trackball, digitizer puck, or other device CD-ROM drive: Any speed (for installation only) Browser: Internet Explorer 6.0 minimum Optional equipment: A printer or plotter; a digitizing tablet; a network interface card if you re using the network version of AutoCAD, or Internet-enabled features of AutoCAD

Use the same step-size and simulation duration as in part (d.1).

What resources useful for the online business does the organisation control at the moment What new resources are needed t o achieve success and to fulfil o u r strategic aims What are the priorities for these new resources This is particularly relevant as accumulating one resource is likely t o affect ~- and possibly deplete - other resources. H o w can we acquire new resources In particular, how can the web site be used to develop new resources and strengthen existing ones Underlying all of these issues is the question of relativity: the resource base needs to be effective in relafiorz to the organisation s competitors.

Use xrange for looping across long ranges; it uses much less memory than range, and may save time as well. Both versions are likely to be faster than a while loop:

Figure 21-6: Setting a second marker to jump to a desired close-up. Another is set to just before a video track ends. (The blue arrow is the cursor.)

PA, 123 tert-Butyl cation ``Y''-conjugation, 304 tert-Butyl carbanion, 109 tert-Butylhydroperoxide, 11 2-Butyne, 296 ``C'' substituents electrophilic addition alkenes, 101 102 benzenes, 155 156 interaction with CbbC, 100 C H, 143, 145 CbbO, 122 carbanion, 109 carbene, 115 carbocation, 106 carbon radical, 111 nitrene, 117 nitrenium, 119 list of, 102 C18 , 151 C60 , 151 Cannizzaro reaction, 84, 146 formaldehyde, 146 Captodative e ect, 113, 277 Carbalkoxycarbenes (:CRCO2 R), 116 Carbanions, 108 110 bases and nucleophiles, 97 gas phase, 109 substituents on, 109 a-sulfonyl, 277 Carbene, see also Methylene :CBr2 , 115 :C(CH3 )2 , 116 :CCl2 , 115 :CClOCH3 , 115 :CF2 , 115 :CFOCH3 , 115 :CHCCH, 116 :CHC6 H5 , 116 :CHCHO, 116 :CHF, 115 :CI2 , 115 :C(OCH3 )2 , 115 :CRCO2 R, 116 Carbenes, 114 116 addition to alkenes, 207 208 C H insertion, 208 dimerization, 208 electronic states, 114 singlet reaction with carbonyl, 279

Figure 14-2

vN(r)

3 2 1 0 7 6 5 4

6.3 s 300

Figure 15.5. Dauben Salem Turro analysis of the photochemical step of the Norrish Type II reaction. The reaction is e cient on the 3 np surface to yield triplet diradical products. It is less e cient on the 1 np surface since IC is relatively e cient.

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