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Aluminum electronegativity

Chauvin, Y., Di Marco-Van Tiggelen, E, and Olivier, H., Determination of aluminum electronegativity in new ambient-temperature acidic molten salts, J. Chem. Soc., Dalton Trans., 1009-1011,1993. [Pg.348]

Aluminum electronegativities for various mixtures have been determined by Chauvin et al. [23]. The group used a combination of NMR and the applicahon of modified Dailey-Shoolery equations. In this fashion, composihon-independent electronegativities of 1.43 could only be determined for basic melts. The electronegativihes in acidic melts were strongly dependent on the melt composition, ranging from 1.2 to 1.6. [Pg.360]

Since electronegative groups at C-20 or C-21 deactivate a A hdouble bond towards attack by osmium tetroxide, Swiss workers have devised procedures wherein these groups are first reduced with lithium aluminum hydride, and the resulting aluminum complexes are then treated with osmium tetroxide... [Pg.218]

B Aluminum forms an amphoteric oxide in which it has the oxidation state +3 therefore, aluminum is the element. 14.3B Hydrogen is a nonmetal and a diatomic gas at room temperature. It has an intermediate electronegativity (x — 2.2), so it forms covalent bonds with nonmetals and forms anions in combination with metals. In contrast, Group 1 elements are solid metals that have low electronegativities and form cations in combination with nonmetals. [Pg.979]

Selenoaldehydes 104, like thioaldehydes, have also been generated in situ from acetals and then directly trapped with dienes, thus offering a useful one-pot procedure for preparing cyclic seleno-compounds [103,104], The construction of a carbon-selenium double bond was achieved by reacting acetal derivatives with dimethylaluminum selenide (Equation 2.30). Cycloadditions of seleno aldehydes occur even at 0 °C. In these reactions, however, the carbon-selenium bond formed by the nucleophilic attack of the electronegative selenium atom in 105 to the aluminum-coordinated acetal carbon, may require a high reaction temperature [103], The cycloaddition with cyclopentadiene preferentially gave the kinetically favorable endo isomer. [Pg.71]

The electronegativity of aluminum is 1.61 and that of silver is 1.93. Which of these two metals is the stronger reducing agent ... [Pg.153]

The metallic impurities present in an impure metal can be broadly divided into two groups those nobler (less electronegative) and those less noble or baser (more electronegative) as compared to the metal to be purified. Purification with respect to these two classes of impurities occurs due to the chemical and the electrochemical reactions that take place at the anode and at the cathode. At the anode, the impurities which are baser than the metal to be purified would go into solution by chemical displacement and by electrochemical reactions whereas the nobler impurities would remain behind as sludges. At the cathode, the baser impurities would not get electrolytically deposited because of the unfavorable electrode potential and the concentration of these impurities would build up in the electrolyte. If, however, the baser impurities enter the cell via the electrolyte or from the construction materials of the cell, there would be no accumulation or build up because these would readily co-deposit at the cathode and contaminate the metal. It is for this reason that it is extremely important to select the electrolyte and the construction materials of the cell carefully. In actual practice, some of the baser impurities do get transferred to the cathode due to chemical reactions. As an example, let the case of the electrorefining of vanadium in a molten electrolyte composed of sodium chloride-potassium chloride-vanadium dichloride be considered. Aluminum and iron are typically considered as baser and nobler impurities in the metal. When the impure metal is brought into contact with the molten electrolyte, the following reaction occurs... [Pg.716]

Metals more electronegative than magnesium, like beryllium, zinc, cadmium and mercury, form useful reagents for specific purposes, but the metals themselves are not sufficiently active to form organic derivatives under normal laboratory conditions and are unwanted in the environment since they are toxic. Aluminum compounds are useful for industrial purposes, but their use in the laboratory is insignificant in comparison with Grignard reagents. [Pg.103]


See other pages where Aluminum electronegativity is mentioned: [Pg.507]    [Pg.298]    [Pg.149]    [Pg.258]    [Pg.67]    [Pg.741]    [Pg.148]    [Pg.353]    [Pg.367]    [Pg.10]    [Pg.4]    [Pg.22]    [Pg.24]    [Pg.31]    [Pg.40]    [Pg.41]    [Pg.44]    [Pg.55]    [Pg.249]    [Pg.158]    [Pg.348]    [Pg.136]    [Pg.361]    [Pg.363]    [Pg.118]    [Pg.47]    [Pg.556]    [Pg.122]    [Pg.146]    [Pg.422]    [Pg.70]    [Pg.42]    [Pg.125]    [Pg.141]    [Pg.142]    [Pg.249]    [Pg.274]    [Pg.43]    [Pg.63]    [Pg.87]    [Pg.111]    [Pg.239]   
See also in sourсe #XX -- [ Pg.54 , Pg.55 ]




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