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Statistically, this would produce a reasonably wellbalanced partitioning Note that for the PDA, the result has a different structure compared to the CDA The PDA generates bi-level blocks with one parent and potentially multiple children, while the CDA generates bi-level blocks with one or zero blocks per parent The task is now to design an ef cient algorithm that classi es a given bi-level as suitable for either the CDA or the PDA This algorithm s job is to switch automatically and transparently between the two approaches, always producing a high-quality result Because the CDA generally gives high-quality results, a goal for the classi cation algorithm is to classify as many bi-levels as possible as suitable for the CDA A crucial constraint is that it should never classify an impossible bi-level to the CDA as this will cause Nature+Fable to fail.

Figure 7-10: Spell checking can be performed on comment text notes and form fields only. Checking body text in the PDF is not supported.

We also want the classi cation algorithm to conform to the general Nature+Fable algorithm policy regarding ef ciency; that is, for signi cantly complex tasks, we prefer powerful heuristics over searching for an exact or optimal solution While deriving and computing mathematical quantities for classifying a bi-level might be possible and bears the potential of rigorous results, we considered this prohibitively expensive Instead, we constructed a conceptually trivial, yet powerful, recursive algorithm that singles out bi-levels that are trivial to classify If trivial classi cation fails, the bi-level is split and both resulting parts are classi ed recursively..

e ective electronegativity of nearby carbon atoms and therefore stabilize a negative charge. An orbital interaction diagram for stabilization by p-type delocalization of the carbanionic lone pair is shown in Figure B7.1c. All C F bonds to the carbanion site stabilize the carbanion by negative hyperconjugation. The group molecular orbitals of the tri uoromethyl group are shown in Figure B7.1b, as seen down the three-fold symmetry axis (see also Figure 3.20). Because of the electronegativity di erence between C and F, the C F antibonding orbitals are highly polarized toward the carbon atom and are low lying; both factors strengthen the p-type interaction between nC and one of the degenerate pairs of s orbitals. It usually happens that the degeneracy is broken, with one bond being selected, s2 in this case. The broken three fold symmetry and pyramidalization at the carbanion site (i.e., nC is sp n rather than pure p) permit a favorable secondary interaction with the lowest lying empty group orbital, s1 , shown by a dashed line in Figure B7.1c. Because the dominant interaction is p type, and because the bonding orbitals (not shown) are

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