Magnesium displacement

The clay minerals carried by rivers into the ocean represent a net annual addition of 5.2 X 10 mEq of cation exchange capacity. Most of these exchange sites are occupied by calcivun. Within a few weeks to months following introduction into seawater, sodium, potassium, and magnesium displace most of the calcium. As shown in Table 21.7, this uptake removes a significant fraction of the river input of sodium, magnesium, and potassium. 

Magnesium displaces copper from a dilute solution of cop-per(II) sulfate the pure copper will settle out of the solution. 

The rivers also carry clay minerals into the ocean. The cation exchange capacity corresponds to 5.2 10 meq y. This may be compared with the river input of cations of 41 10 meq y (1.302 meq 1 from Table 2 in a flow of 10 m s ). In the ocean the sodium, potassium, and magnesium displace calcium in the clay minerals by ion exchange. 

Adsorption by Clays. — Owing to the possibility of chemical reactions between the clay and the adsorbed substances, the phenomena here are much more complicated than is ordinarily the case with many colloidal systems. According to Sullivan changes between the radicals are often involved. For instance when acid or neutral salts are adsorbed, sodium, potassium, and magnesium from the clay may be released or dissolved, while an equivalent amoimt of the adsorbed basic radical remains with the clay. The addition of alkaline solution is still more complicated. Not only may there be free alkali but basic solutions may be formed because of the hydrolysis of salts of a strong base and a weak acid, e.g., carbonates and phosphates. Three different reactions are now possible. First, the free alkali may react with the colloidal silica. Second, the silicate radical from the clay may form insoluble salts with the adsorbed base. Third, the sodium, potassium, or magnesium displaced from the clay may form soluble carbonates and phosphates, and these salts in turn be adsorbed by the clay constituents. These reactions are of great importance in the study of the fertilization of the soil. It has been claimed that the addition of lime not only neutralizes the undesirable acids, but also renders the potassium of the clay available for the plant. 

Relative intensities and displacement of the various lines in the Kq X-ray spectrum of magnesium relative to the Kd.s line (adapted by permission of Physical Electronics Corp. from Ref. [21])... 

Chloro-5,6-diphenyl-as-triazine readily undergoes methoxy-de-chlorination at 25° (< 12 hr) with methanolic methoxide and at 65° (4.5 hr) in non-basified methanol. The chloro group is also displaced by hydrazine (80°, 1 hr), ammonia (140°, 6 hr), and phenyl-magnesium bromide (70°, 12 hr), the latter forming the triphenyl compound 315.3-Chloro-6-phenyl-as-triazine is unstable to cold water or alkali and to hot alcohol or aqueous potassium carbonate. ... 

An interesting appetite suppressant very distantly related to hexahydroamphetamines is somanta-dine (24). The reported synthesis starts with conversion of 1-adamantanecarboxylic acid (20) via the usual steps to the ester, reduction to the alcohol, transformation to the bromide (21), conversion of the latter to a Grignard reagent with magnesium metal, and transformation to tertiary alcohol 22 by reaction with acetone. Displacement to the fomiamide (23) and hydrolysis to the tertiary amine (24) completes the preparation of somantadine [6]. 

An ester of alanine with an arylaliphatic alcohol has shown promise as a non-tricyclic antidepressant. It may be speculated that the hindered milieu of the ester linkage protects the compound from hydrolysis by endogenous esterases. The preparation starts by reaction of pheny-lacctate 83 with methyl magnesium iodide to give tertiary carbinol 84. Acylation with 2-bromo-]>ropionyl bromide leads to ester 85 displacement of halogen with ammonia leads to alaproclate ( 6) [211. 

When metals are arranged in the order of their standard electrode potentials, the so-called electrochemical series of the metals is obtained. The greater the negative value of the potential, the greater is the tendency of the metal to pass into the ionic state. A metal will normally displace any other metal below it in the series from solutions of its salts. Thus magnesium, aluminium, zinc, or iron will displace copper from solutions of its salts lead will displace copper, mercury, or silver copper will displace silver. 

An interesting application is the titration of calcium. In the direct titration of calcium ions, solochrome black gives a poor end point if magnesium is present, it is displaced from its EDTA complex by calcium and an improved end point results (compare Section 10.51). 

Mixtures of manganese, magnesium, and zinc can be similarly analysed. The first EDTA end point gives the sum of the three ions. Fluoride ion is added and the EDTA liberated from the magnesium-EDTA complex is titrated with manganese ion as detailed above. Following the second end point cyanide ion is added to displace zinc from its EDTA chelate and to form the stable cyanozincate complex [Zn(CN)4]2- the liberated EDTA (equivalent to the zinc) is titrated with standard manganese-ion solution. 

Two absorbents are required, one for water vapour, the other for carbon dioxide. The absorbents for water vapour which are generally employed are (a) anhydrous calcium chloride (14-20 mesh), (b) anhydrous calcium sulphate ( Drierite or Anhydrocel ), and (c) anhydrous magnesium perchlorate ( Anhydrone ). Both (b) and (c) are preferable to (a) (c) absorbs about 50 per cent of its weight of water, but is expensive. Anhydrous calcium chloride usually contains a little free lime, which will absorb carbon dioxide also it is essential to saturate the U-tube containing calcium chloride with dry carbon dioxide for several hours and then to displace the carbon dioxide by a current of pure dry air before use. 

Alkyl, aryl, and allyl derivatives of boron can be prepared directly from the corresponding halides, BF3, and magnesium metal. This process presumably involves in situ generation of a Grignard reagent, which then displaces fluoride from boron.2... 

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