Ion exchange and solvent extraction of metal complexes (Marcus, Y

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b00k reviews from those in the expanded version. The answer8 to the numerical problems are given. An adequate index is included. The passage on potentiomet,ric titrations has been moved from the materid on electrochemical methods t,o the chapter on oxidation-reduot,ion methods. In conjunction wit,h this move a "figure" error ocn~rred. A glass membrane electrode is shown instead of the stated satomted calomel electrode. The parent, edition was somewhat of a departure from a traditional quantitative analysis text-both by the types and depth of matter included. The authors in their desire to produce a. less rigorous text have accomplished their goal; however, in so doing have created a text, that has last much of its earlier citement" or advantages. Both texts are adequate for s. one-semester quantitative analysis course, with the expanded version still not suitable for a separate tev instrumental-type eourse. With this last point in mind a11d the difference in price being only a few dollsrs, the reviewer prefers the parent edition. The tional subject matter providesmuch better of the material and allows the instructor greater versatility in planning his course.

Ion Exchonge ond Solvent Extrodion of Metmi complexes

Y. Alarczu, and A . S. Kertes, Hebrew Univemity of Jerusalem, Israel. Interscience Publishers (a division of John Wiley & Sons, Inc.), New York, 1969. ix + 1037 pp. Figs. and tables. 16 x 23.5 em. $44.9.5.

A rigorous and detailed examination of the thermodynamics of metal complex formation provides the leitmotif for this massive, mholal.ly contribution of two Israeli seientifit,~in which the complementary techniques of solvent extraction and ion exchange are described. Marcus and Kert,es, themselves active researchers in these fields, provide a firm foundation for the thermodynamic aspects ,of t.he two important separation techniques in the first quarter of their hook where, in three chapters, the t,hermodynamics of aqueous and non-aqueous eleotrolgte solutions are presented. Thorny prohlemn snch as the quantitative consideration of concentrated and mixed electrolyte aqlleous salutiona as well as mixed solvent and aggregation (including micelle formation) in organic solvents are presented and dealt with in a competent, "present state of the art" approach. The mathematical appamtufi for dealing with complex formation equilibria with particr~lar emphasis on the delicate decisions required to distinguish hebween true complex formatiall and J. M. PAPPENHAGEN"lreachemu~" activity effectsis presented. Kenym College After a chapter dealing with ion exGambier,Ohio changers, ttheir swelling and sorption

equilibria, as well a5 exchange phenomeua occurring in concentrated solutions and mired solvents, there follows twin chapters dealing with the many ramifications of the use of cation and anion exchange to determine the equilibrium constants of metal complex formation. The use of solvent extraction in stndying metal complex equilibria receives a similar treatment. The authors organize extraction systems inio the following categories and devote a chapter to each: Extraction by (1) compound formation (chelates, acidic organophosphorus compounds, salts of earboxylic and sulfonic phosacids), (2) solvation (carbon-r phorus-bonded oxygen-donor solvents, (3) ion-pair formation (use of quaternary ammonium, phosphonium, and xrsoninm salts), and (4) syuergism (mixed ligand systems). The hook is well organized and each of the twelve chapters has a detailed summary of the viewpoint and the content of the text material. There are occasional examplea of the need far better integration of the material in various sections of the hook. For example, after a, fourpage exposition on the nature and use of the solubility parameter the aothars repudiate the validity of its u w with "polar" substances. Later in the text, however, solubility parameter considerations are freely employed. Again, in the section on dithisone they espouse the outmoded and incorrect Fischer stmcture of primary chelates (involving only nitrogen-metal bonding) despite their

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all age8 in areas of the biochemical ssiences have undoubtedly experienced t,he frustrations of restudying quantitative citations of Irving's work, f t u n which the aspects of our subject matter by returning cutxmt formulation (with N- and S-metal to undergraduate bext books. We may bonding) stems. Yet in n brief discussion have forgotten how to determine the of tho formation of zinc dithiaon%teelseantilog of 3.6020, t,he yalne of R, ionic where, they refer to the bonding of metal strength equations, the concept of ento sulfur as m e of the primary steps. tropy, the specific activity of pure carbonPerhaps it is not, entirely fair to expect, 14, or the graphics of competitive and nona 1037-page hook to be a treatise rather competitive inhibition of enzyme activity. than a monograph. I t is after all a iribute These and many other aspects of the l o the imporlance of these fields and to the quantitative treatment of biochemical intense, widespread interest they generate data are outlined in this relatively small i t , the scientific community to note ahat, book. even the almost three t,hausand references The thirteen chapters are organized into employed here could be augmented by an three sections. The first contains chapequal mtmber before tho topics could be tera on logarithms, algebraic equations, considered to be exhaustively treated. I t stat,istical methods, and stoichiometrical is n book that will he well-worn by d l the problems. All bhose quantitative aspects research groups working in these fields. normally expected in s biochemistry I t is deplorable that their publishers laboratory manual, including treatments practieallv guarantee that gmdoate stxof thermodynamics and enzyme kinetics denbs, whom the nulhors consider an imare found in the second part. Spectroportant segmeut of their audience, will be photometly and radiochemistry are predeprived of pemonal copies of this book. sented in the find section. Each chapter concludes wit,h t,wo sets of questions for H ~ R FREI~KR Y bhe student, with detailed solutions given University of Arizona for the first set only. This is 8.11 obvious Tucson bonus, as it allows t,he book to he osed as a Quantitative Problems in the text as well as areference book. Biochemical Sciences The authors think of this book as a companion text, covering subject matter Rez Montgomery and Charles A . Swenson, that. is supplemental to t,hat presented in both of University of Iowa, Iowa. City. beginning graduate level courses. Most W. H. Freeman and Co., Sen Francisco, d of the material h, this book s h o ~ ~ lhave 1969. xiii 308pp. Figs. and tables. been treated in undergraduate courses in 15.5 X 23.5 em. Softhonnd. $2.95. mathematics, physics, or analytical and physical chemistry, so from this viewpoint, Graduate and postgraduate students of

book reviews

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it is a reference and remedial study book. In either case, the unique variety of quantitative tools discussed and the effective and precise methods of presentation make the book a very vduable addition to any biochemically oriented laboratory or c l a w room bookshelf.

W. BERNLOHR ROBERT Universitg of Minnesota Minneapolis Problems in Organic Reaction Mechanisms

F . 31'. Menger, Emory University, Atlanta, Georgia. Appleton-Century121 pp Crafts, New Yark, 1969. vii Figs. and tables. 18.5 X 25.5 cm. Softbound $2.95.

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This inexpensive book consists of fifty-five reactions involving a great variety of types for which the stndent is to wo1.k out suitable mechanisms. Few of the problems can be solved simply by inspection. The student can check his answers against the answers provided. Far the first twenty answers detailed remarks are given while for the last thirtyfive, the mechanisms are presented without comment. In addition, a lit,erature reference from which the reaction and/or reaction meehsnism wits taken is given for each problem. This book is not. designed for the beginning organic stndent to use as he progresses throogh his fin1 organic course.

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