Base strength table

Potassium Alkoxides. The most widely used potassium bases are potassium tert-hu. oAde [865-47-4] (KTB) and potassium / i -amylate [41233-93-6] (KTA). These strong alkoxide bases offer such advantages as base strength (pX = 18), solubiUty (Table 5), regio/stereoselectivity because of bulky alkyl groups, and stabiUty because of the lack of a-protons. On storage, KTB and KTA have long shelf Hves under inert atmosphere (see... 

Because of their diverse stmctures, there are few common threads to vitamin chemical properties aside from their fat or water solubiUty. Of general concern ia all appHcations, however, is vitamin stabiUty. Table 5 provides generic iaformation regarding stabiUty under several conditions. Levels of stabiUty vary greatly and are impacted by acid or base strength, light iatensity, etc. 

There is also evidence for stable 3,4-adducts from the X-ray analysis of 2-amino-4-ethoxy-3,4-dihydropteridinium bromide, the nucleophilic addition product of 2-aminopteridine hydrobromide and ethanol (69JCS(B)489). The pH values obtained by potentiometric titration of (16) with acid and back-titration with alkali produces a hysteresis loop, indicating an equilibrium between various molecular species such as the anhydrous neutral form and the predominantly hydrated cation. Table 1 illustrates more aspects of this anomaly. 2-Aminop-teridine, paradoxically, is a stronger base than any of its methyl derivatives each dimethyl derivative is a weaker base than either of its parent monomethyl derivatives. Thus the base strengths decrease in the order in which they are expected to increase, with only the 2-amino-4,6,7-trimethylpteridine out of order, being more basic than the 4,7-dimethyl derivative. 

Table 6.S. Orientation in E2 Elimination as a Function of Base Strength...

Adolph Baeyer is credited with the first recognition of the general nature of the reaction between phenols and aldehydes in 1872 ([2,5-7] [18], Table 5.1). He reported formation of colorless resins when acidic solutions of pyrogallic acid or resorcinol were mixed with oil of bitter almonds, which consists primarily benzaldehyde. Baeyer also saw resin formation with acidic and basic solutions of phenol and acetaldehyde or chloral. Michael and Comey furthered Baeyer s work with additional studies on the behavior of benzaldehyde and phenols [2,19]. They studied a variety of acidic and basic catalysts and noted that reaction vigor followed the acid or base strength of the catalyst. Michael et al. also reported rapid oxidation and darkening of phenolic resins when catalyzed by alkaline materials. 

Table 24.1 lists pXa values of some ammonium ions and indicates that there is a substantial range of amine basicities. Most simple alkylainines are similar in their base strength, with p/q/s for their ammonium ions in the narrow range 10 to 11. Aiylctmines, however, are considerably less basic than alkylamines, as are the heterocyclic amines pyridine and pyurole. 

Moving down in a column is equivalent in many respects to moving to the left in the periodic table. Since we find basic properties predominant at the left of the periodic table in a row, we can expect to find basic properties increasing toward the bottom of a column. Thus the base strength of the alkaline earth hydroxides is expected to be largest for barium and strontium. The greatest acid strength is expected for beryllium hydroxide. 

TABLE 8.6 Bases Listed in Increasing Order of Base Strength when Compared with Certain Reference Acids... 

A striking result of this reinvestigation (128, 129) is the observation that the ratio of the product ketone to the acetylene formed from a-bromo-p-aminostyrene is a function of the pH (Table Vll) but that the rate at which they are formed is not. As the pH increases from 3.9 to 13.1, the relative yield of acetylene increases from 16% to 85%. Therefore, the acetylene formation by elimination of a proton from the vinyl cation (path b in route D in Scheme XI) is more susceptible to an increase in base strength than is ketone formation via the enol (path a). This observation is a rare case of pH control over product composition in a 1-El reaction. 

The tendency for N-nitrosamides to undergo hydrolysis by a nucleophilic catalysed pathway has been confirmed by studies of N-alkylnitroso acetamides (22) Results summarised in Table I for N -n-butyl-JJ -nitroso acetamide show that its decomposition is also subject to steric constraints (2,6-lutidinestrong nucleophiles (eg. imidazole, thiols) irrespective of their base strength (pK ). Further, the second order dependence on [Imidazole] is more clearly defined for the decomposit-... 

Pyridine has practically the same ionization potential as benzene it does not, however, necessarily follow that the flrst ionization potentials (Table 9) relate to an electron of the highest occupied 7r-orbital. These compounds are bases, though weaker than aliphatic amines, and parallels have been noted between base strength and ease of ionization (Nakajima and Pullman, 1958 Krishna and Chowdhury, 1963), which might indicate that the flrst ionization potential is that of a lone-pair... 

Use the table of Ka values in Appendix E to list the conjugate bases of the following acids in order of increasing base strength formic acid, HCOOH hydrofluoric acid, HF(aq) benzoic acid, CeHsCOOH phenol, CeHsOH. 

I 6 Aspects of Mechanisms, Processes, and Requirements for Zeolite Separation Table 6.5 Base strengths of aromatic hydrocarbons relative to HF. 

Baba and Endou 117) reported that CaO is an active catalyst for isomerization of VBH to EBH when it is evacuated at temperatures above 800 K, whereas MgO did not show any activity for this process. However, some discrepancies have been reported by Kabashima et al. 10), who found that MgO, CaO, SrO, and BaO catalyze the isomerization of VBH to EBH, with the order of activity being CaO > MgO > SrO > BaO. This order in activity is attributed to the trends in base strength of oxides (BaO > SrO > CaO > MgO) and the surface area, the latter decreasing in the order MgO > CaO > SrO > BaO (Table II). The activity of the CaO was the highest among these alkaline earth metal oxides, and the activity of the MgO varied with the pre-treatment temperature, reaching a maximum it was 873 K ... 

Additional comparisons between calculated and experimental relative base strengths are found in Appendix A6 (Tables A6-48 and... 

Table 2 values of some acids at 25 °C 4.2. BASE STRENGTH... 

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