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Theses/Dissertations

Chemistry

University of New Mexico

1950

Articles 1 - 9 of 9

Full-Text Articles in Physical Sciences and Mathematics

The Kinetics Of The Exchange Between Sn(Ii) And Sn(Iv) In Absolute Alcohol, E. Gerald Meyer Nov 1950

The Kinetics Of The Exchange Between Sn(Ii) And Sn(Iv) In Absolute Alcohol, E. Gerald Meyer

Chemistry and Chemical Biology ETDs

In the present work use was made of the radiochemical exchange reaction to study the kinetics of the reaction

SnCl2 + Sn*Cl4 = Sn*Cl2 + SnCl4

in an absolute alcohol medium. A rate equation was established as a function of concentration and temperature, and some predictions were made regarding the mechanism.


Some Reactions Of 4-Chlorocinnoline, F. H. Kruse Oct 1950

Some Reactions Of 4-Chlorocinnoline, F. H. Kruse

Chemistry and Chemical Biology ETDs

This problem involves the preparation of 4-chlorocinnoline by the method of Borshe and Herbert and Busch and Rast,, and the study of further replacement reactions of the chlorine atom in the 4-position. The problem can be subdivided into two sections: (1) the preparation of the 4-cinnolyl Grignard reagent and the corresponding lithium compound and (2) the study of some condensation reactions of 4-chlorocinnoline.


An Analytical Study Of Berberine, W. Riley Mcgaughran Aug 1950

An Analytical Study Of Berberine, W. Riley Mcgaughran

Chemistry and Chemical Biology ETDs

Berberine, an alkaloid, has unique pharmacological properties as well as unusual chemical and physical characteristics. This compound has been used for many years as a remedy for eye diseases. In contrast to most alkaloids, berberine hydroxide is more soluble than its salts. Its chemical structure has been established, but a correlations of many of its properties and its structures has not been made.

The purpose of this work was to undertake an analytical study of berberine, hoping to collect data which would make possible the correlation of certain properties of the compound with its structure. The study was planned to …


A Study Of The Use Of The Dicyanatodipyridine (Ii) Complex For The Determination Of Cyanate, Jean Mcclelland May 1950

A Study Of The Use Of The Dicyanatodipyridine (Ii) Complex For The Determination Of Cyanate, Jean Mcclelland

Chemistry and Chemical Biology ETDs

Treadwell states in his text, Analytical Chemistry, Volume II, that "the only method for examining cyanates consists in determining the amount of carbon and nitrogen present by combustion." A review of the available literature shows that, although this is not literally true, a procedure for this quantitative determination of small amounts of cyanates in the presence of interfering substances is lacking.

A survey of the literature yielded few references for instrumental methods for the quantitative determination of cyanates. Ripan-Tilici published a method for the determination of cyanates poteniometrically, but attempts to duplicate her work have failed. Madame Tilici, in …


The Syntheses And Ultraviolet Absorption Spectra Of 2-Imidazolines, 2-Imidazolidones And Imidazolidines, Robert J. Ferm May 1950

The Syntheses And Ultraviolet Absorption Spectra Of 2-Imidazolines, 2-Imidazolidones And Imidazolidines, Robert J. Ferm

Chemistry and Chemical Biology ETDs

The first method used to prepare 2-imidazolines was through the reaction of aromatic aldehydes with ammonia. Amarin, which is known as 2,4,5-triphenyl-2-imidazoline, was the first compound reported to be prepared in this manner. This type of reaction has since been widely studied 2,3,4,5,6 in connection with the preparation of 2,4,5-triarylimidazolines. Furfural and ammonia have also been reported to react in a similar manner. Amarin has also been obtained from the reaction of a mixture of benzil, ammonia, and benzaldehyde.


The Preparation And Properties Of Aromatic Ditellurides, Roger Sanftner May 1950

The Preparation And Properties Of Aromatic Ditellurides, Roger Sanftner

Chemistry and Chemical Biology ETDs

All attempts to arrive at a conclusion as to the structure of the ditellurides by chemical means were unsuccessful. It was found that the ditelluride either failed to enter into reaction, or it reacted with the elimination of tellrium. It is thought, however, that a spectrophotometric analysis of the bromine addition would furnish some information concerning the ditelluride structure.


The Chelation Of Praseodymium As A Function Of Ph Using Thenolytrifluoroacetone, Thomas K. Keenan May 1950

The Chelation Of Praseodymium As A Function Of Ph Using Thenolytrifluoroacetone, Thomas K. Keenan

Chemistry and Chemical Biology ETDs

The rare earth elements, including elements 57 through 71, provide many diverse series of studies through their chemical reactions. In as much as these elements are all in Group III of the periodic table, they are markedly similar in their properties. The separation, insulation and purification of the various rare earths from one another has long been a problem of great interest to the chemist.


A Study Of The Intermediary Products Formed During The Life Of A Copper Cyanide Plating Bath, Matthew E. Carlisle May 1950

A Study Of The Intermediary Products Formed During The Life Of A Copper Cyanide Plating Bath, Matthew E. Carlisle

Chemistry and Chemical Biology ETDs

Four aims of a study of cyanide baths were:

1. To study the intermediate products formed during the operation of plating and stripping baths under various conditions.

2. To identify these intermediate products or complexes and to determine whether or not they caused the failure of the bath.

3. To consider the conditions that caused a bath to fail, and to be able thereby to increase the life of the bath.

4. To develop a fast, accurate method for controlling the baths, preferably by means of the cyanide content.


The Use Of Ethyl 4,4-Dimethyl-1-Isopropyl-2-Imidazolinyl-2-Acetate In The Synthesis Of Some 2-Imidazolines, Jacob Shapira May 1950

The Use Of Ethyl 4,4-Dimethyl-1-Isopropyl-2-Imidazolinyl-2-Acetate In The Synthesis Of Some 2-Imidazolines, Jacob Shapira

Chemistry and Chemical Biology ETDs

One equivalent of N-(2-aminoisobutyl)-isopropyl-amine (I) was allowed to react with diethyl malonate to produce ethyl 4,4-dimethyl-1-isopropyl-2-imidazolinyl-2-acetate (II) in various yields which depended mainly on the temperature, time allowed for the reaction, and the method of isolation from the reaction mixture.