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Leaving basicity

While the number of UB II beneficiaries increased strongly, data on individual benefit spells in 2005 show that there is considerable mobility in and out of UB II (Graf and Rudolph 2006 Graf 2007). About 74% of all households in need in January 2005 depended on benefits throughout the year while 26% were able to leave UB II. Households entering UB II later in 2005 had a higher chance of leaving basic income support within 12 months (43%). Continued benefit dependency over 12 months was most frequent with lone parents who could opt for an exemption from the job search requirement. [Pg.53]

At this point the reader may feel that we have done little in the way of explaining molecular synnnetry. All we have done is to state basic results, nonnally treated in introductory courses on quantum mechanics, connected with the fact that it is possible to find a complete set of simultaneous eigenfiinctions for two or more commuting operators. However, as we shall see in section Al.4.3.2. the fact that the molecular Hamiltonian //coimmites with and F is intimately coimected to the fact that //commutes with (or, equivalently, is invariant to) any rotation of the molecule about a space-fixed axis passing tlirough the centre of mass of the molecule. As stated above, an operation that leaves the Hamiltonian invariant is a symmetry operation of the Hamiltonian. The infinite set of all possible rotations of the... [Pg.140]

In the former, it gives precipitates with halides (except the fluoride), cyanides, thiocyanates, chromates(VI), phosphate(V), and most ions of organic acids. The silver salts of organic acids are obtained as white precipitates on adding silver nitrate to a neutral solution of the acid. These silver salts on ignition leave silver. When this reaction is carried out quantitatively, it provides a means of determining the basicity of the acid... [Pg.430]

It is again assumed that the neutral substance is insoluble in water (see, however, the footnote on p. 389). The separation now consists in extracting the mixture with diL HCl, which dissolves the basic component, leaving the undissolved neutral component. [Pg.400]

Acetates may also be prepared by adding acetic anhydride to somewhat dilute solutions of compounds containing hydroxyl (or amino) groups in aqueous caustic alkahs. The amount of alkali used should suffice to leave the hquid shghtly basic at the end of the operation, so much ice should be added that a little remains unmelted, and the acetic anhydride should be added quickly. [Pg.682]

Notice too that strongly basic leaving groups are absent from Table 8 8 In gen eral any species that has greater than about 2 for its conjugate acid cannot be a... [Pg.352]

Once It was established that hydroxide ion attacks the carbonyl group in basic ester hydrolysis the next question to be addressed concerned whether the reaction is concerted or involves a tetrahedral intermediate In a concerted reaction the bond to the leaving group breaks at the same time that hydroxide ion attacks the carbonyl... [Pg.855]

Although the compounds were isolated in quantities of only a few milligrams per kilogram of cmde plant leaves, extensive work on a variety of animal tumor systems led to eventual clinical use of these bases, first alone and later in conjunction with other materials, in the treatment of Hodgkin s disease and acute lymphoblastic leukemia. Their main effect appears to be binding tightly to tubuHn, the basic component of microtubules found in eukaryotic cells, thus interfering with its polymerization and hence the formation of microtubules required for tumor proliferation (82). [Pg.552]

Filament yam is produced basically by the same process except that the spinning machine is so constmcted as to prevent individual yams leaving spinnerets from contacting each other. [Pg.338]

The unshared pairs of electrons on hydroxyl oxygens seek electron deficient centers. Alkylphenols tend to be less nucleophiUc than aUphatic alcohols as a direct result of the attraction of the electron density by the aromatic nucleus. The reactivity of the hydroxyl group can be enhanced in spite of the attraction of the ring current by use of a basic catalyst which removes the acidic proton from the hydroxyl group leaving the more nucleophiUc alkylphenoxide. [Pg.59]


See other pages where Leaving basicity is mentioned: [Pg.191]    [Pg.172]    [Pg.204]    [Pg.345]    [Pg.191]    [Pg.172]    [Pg.204]    [Pg.345]    [Pg.178]    [Pg.35]    [Pg.889]    [Pg.2242]    [Pg.19]    [Pg.872]    [Pg.146]    [Pg.53]    [Pg.59]    [Pg.126]    [Pg.330]    [Pg.351]    [Pg.352]    [Pg.839]    [Pg.944]    [Pg.1139]    [Pg.377]    [Pg.240]    [Pg.533]    [Pg.88]    [Pg.331]    [Pg.312]    [Pg.119]    [Pg.233]    [Pg.38]    [Pg.263]    [Pg.319]    [Pg.375]    [Pg.295]    [Pg.311]    [Pg.30]    [Pg.209]    [Pg.217]    [Pg.217]    [Pg.7]    [Pg.375]    [Pg.457]   
See also in sourсe #XX -- [ Pg.81 ]




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