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The last approximation in equation (4.1) is only really valid for the small-overlap regime, which this is not, but it serves to remind us of the approximately inverse energy dependence of the stabilization. One may ask how hE het would be expected to change in the series C C, C N, C O, and C F or the series H C, H N, H O, and H F. In the crudest approximation, one may say that the orbitals of C, N, O, and F are all approximately the same size and therefore the interaction matrix element hAB will be approximately the same size for any A B pair. The dominant factor determining the heterolysis energy therefore is the di erence in orbital energies in the denominator, and one has directly the prediction (Figure 4.2) that ease of heterolytic cleavage for C X is in the order C b N b O b F. The C C bond is least likely to dissociate heterolytically and the C F bond the most likely. In an absolute sense, of course, heterolytic cleavage is not a likely process for any of these bonds in the absence of other factors, as discussed below. Similarly, one may ask how hE het would be expected to change in the series C F, C Cl, C Br, and C I. The situation is more complicated for this series, since both

Creating groups of objects is discussed in the next chapter. Groups are sets of objects that you name. If object grouping is on (the default) when you select one object in a group, all of the objects in the group are automatically selected. Object grouping is a global setting; you can also set object grouping on or off for individual groups.

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similar to ampholines in that they have good and even buffering capacity across a broad range of pH. In this experiment it is possible to achieve selective elution of proteins very close to their pI values. An anion-exchange resin is rst equilibrated at a particular pH (e.g. pH 9.4), followed by amphoteric buffer. This buffer has good buffering capacity across a wide pH range (e.g. 9.0 6.0) and automatically forms a pH gradient through the column in the range 8.3 6.4. Sample proteins are now applied. At the top of the column (pH 6.4), the protein will be positively-charged and will pass freely through the resin without binding but encountering a gradually increasing pH. Eventually, the protein will reach its pI and, soon after this, acquire a negative charge which will allow it to bind to the anion exchange resin. As elution buffer continues to be applied to the column, the pH at the binding site of the protein would be gradually lowered giving the protein again a negative charge and causing it to dissociate from the resin. The protein would elute further down the column until a pH is reached which would again give it a positive charge causing it to bind to the resin once more. In this way, individual proteins move down the column being continuously desorbed and adsorbed as the pH gradient progresses through the resin

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Name LGA 775 Socket 478 Socket 370 Socket 939 Socket 754 Socket A Edge Bleeding/ leading Middle Trailing Bleeding/ leading Middle Trailing Type Intel Intel Intel AMD AMD AMD CPU Families Pentium Extreme Edition (Dual-Core), Pentium D (Dual-Core), Pentium 4 Extreme Edition, Pentium 4, Celeron D Pentium 4 Extreme Edition, Pentium M, Pentium 4, Celeron D Celeron 766 Dual-Core Athlon 64, Athlon 64 FX, Athlon 64 Athlon 64, Sempron Athlon XP, Athlon, Duron, Sempron (Socket A, also known as Socket 462)

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