Dissociation constants of organic bases in aqueous solution [by] D.D. Perrin. Supplement. by Douglas Dalzell Perrin

Cover of: Dissociation constants of organic bases in aqueous solution [by] D.D. Perrin. | Douglas Dalzell Perrin

Published by Butterworths in London .

Written in English

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Subjects:

  • Chemistry, Organic -- Tables, etc.,
  • Dissociation,
  • Electrochemistry

Edition Notes

Book details

Other titlesPure and applied chemistry. Supplement
Classifications
LC ClassificationsQD273 P35 1965 SUPPL.
The Physical Object
Pagination[various pagings]
ID Numbers
Open LibraryOL18509732M

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Ionisation Constants of Inorganic Acids and Bases in Aqueous Solution, Second Edition provides a compilation of tables that summarize relevant data recorded in the literature up to the end of for the ionization constants of inorganic acids and bases in aqueous solution.

This book includes references to acidity functions for strong acids. Get this from a library. Dissociation constants of organic bases in aqueous solution. [D D Perrin]. diSSociation conStantS of organic acidS and BaSeS This table lists the dissociation (ionization) constants of over organic acids, bases, and amphoteric compounds.

All data apply to dilute aqueous solutions and are presented as values of pK a, which is defined as the negative of the logarithm of the equi-librium constant K a for the reaction. Get this from a library.

Dissociation constants of organic bases in aqueous solution. [D D Perrin; International Union of Pure and Applied Chemistry;]. Dissociation constants of inorganic acids and bases in aqueous solution, [Perrin, D. D] on *FREE* shipping on qualifying offers.

Dissociation constants of inorganic acids and bases in aqueous solutionCited by: Dissociation Constants of Organic Bases in Aqueous Solution by D. Perrin (Author) ISBN Format: Paperback. Buy Dissociation Constants of Organic Bases in Aqueous Solution: by Perrin, D. (ISBN: ) from Amazon's Book Store.

Everyday low Author: D. Perrin. Perrin, D.D. () Dissociation Constants of Organic Bases in Aqueous Solution. Butterworths, London. has been cited by the following article: TITLE: Interaction of Iron(III)-5,10,15,Tetrakis (4-Sulfonatophenyl) Porphyrin with Chloroquine, Quinine and Quinidine.

Author of Purification of laboratory chemicals, Organic complexing reagents, Dissociation constants of inorganic acids and bases in aqueous solution, pKa prediction for organic acids and bases, Organic ligands, Ionisation constants of inorganic acids and bases in aqueous solution, Purificaation of laboratory chemicals, Organic complexing reagents.

Perrin, D. (Douglas Dalzell), Title Dissociation constants of organic bases in aqueous solution [by] D. Perrin. Format Book Published London, Butterworths, Description vii,xli p.

26 cm. Other titles Pure and applied chemistry. Supplement. Notes. rows  Dissociation Constants Of Organic Acids And Bases: This table lists the acid-base. Ionization constants of inorganic acids and bases in aqueous solution, second edition.

Author: Perrin, D. Subject: Journal of Chemical Education, Vol. 60 No.5, May pA, Book and Media Reviews Created Date: 8/6/ AMCited by: 5. INORGANIC ACIDS AND BASES IN AQUEOUS SOLUTION D.

PERRIN and also separately as a book*. The Table of organic bases, by the present author, was published in as a supplement to Pure and Applied Chemistry4 For convenience, the dissociation constants of inorganic acids and bases t D. Perrin. Dissociation Constants of Organic File Size: 2MB. Dissociation constants of organic bases in aqueous solution by Perrin, D.

D.,Butterworths edition, in EnglishCited by: Dissociation constants of organic bases in aqueous solution: supplement Douglas Dalzell Perrin, International Union of Pure and Applied Chemistry.

Commission on Electroanalytical Chemistry Snippet view - Perrin, D D. DISSOCIATION CONSTANTS OF INORGANIC ACIDS AND BASES IN AQUEOUS y unknown/Code not available: N. p., Web. doi/pac DISSOCIATION CONSTANTS OF INORGANIC ACIDS AND BASES IN AQUEOUS SOLUTIOND. Perrin, M. Koithoff, Président (u.

A, P. Zuman, Secrétaire (g. (france and D. Perrin}, title = {DISSOCIATION CONSTANTS OF INORGANIC ACIDS AND BASES IN AQUEOUS SOLUTION}, year = {}} Share. OpenURL. Abstract. I How to use the Table II. Perrin has written: 'Ionisation constants of inorganic acids and bases in aqueous solution' -- subject(s): Bases (Chemistry), Dissociation, Inorganic acids, Tables 'Dissociation constants of.

2,5-dimethylaniline is a primary arylamine that is aniline in which the hydrogens at the 2- and 5-positions are replaced by methyl groups.

It is used in the manufacture of dyes and other chemicals. It is a dimethylaniline and a primary arylamine. IUPAC pKa Compilations Converted to Substructure Searchable Databases. Aqueous Solution, by D. Perrin.

Acid 1 Dissociation Constants of Organic Bases in. The dissociation constants of the conjugate acids of 14 amines (diethylethanolamine, monoethanolamine, n-butyldiethanolamine, t-butyldiethanolamine, n,n. An acid dissociation constant, K a, (also known as acidity constant, or acid-ionization constant) is a quantitative measure of the strength of an acid in is the equilibrium constant for a chemical reaction ↽ − − ⇀ − + + known as dissociation in the context of acid–base chemical species HA is an acid that dissociates into A −, the conjugate base of the.

Dissociation Constants of Organic Bases in Aqueous Solution. Perrin, D. Theory of Simple Liquids. Hansen, Jean Pierre; McDonald, Ian R. Low-Energy Neutron Physics. The Book of Alchemy: Learn the Secrets of the Alchemists to Transform Mind, Body and Soul. Melville, Francis. Ralph J. Fessenden and Joan S.

Fessenden, Organic Chemistry, Second Edition B. Lawrence Fox A D. Perrin (Compiler) lonizatlon Constants of Inorganic Acids and Bases in A Aqueous Solution, Second Edition New Volumes in Continuing Series A Titles of Interest A Volume GO Number 5 May AAuthor: B. Lawrence Fox.

[ 22 ] D.D. Perrin, Dissociation Constants of Organic Bases in Aqueous Solution, Butterworths, Lon- don, [23] This book comprises a huge catalogue of analytical methods, 83% of which are pre and out of a total of references only 27 are from on- wards. The basic premise of the text appears to be that chemists can pick up Cited by:   Pure and Applied Chemistry The Scientific Journal of IUPAC.

by Burrows, Hugh / Stohner, Jürgen Dissociation contants of inorganic acids and bases in aqueous solution; Dissociation contants of inorganic acids and bases in aqueous solution. European Journal of Organic Chemistry,VolumeNum Page DOI: Cited by: Dissociation Constants of Inorganic Acids and Bases in Aqueous Solution (International Union of Pure and Applied Chemistry) Perrin, D.

Published by Butterworth &. Pseudoephedrine is a member of the class of the class of phenylethanolamines that is (1S)(methylamino)phenylethanol in which the pro-S hydrogen at position 2 is replaced by a methyl group.

It has a role as a sympathomimetic agent, an anti-asthmatic drug, a bronchodilator agent, a vasoconstrictor agent, a central nervous system drug, a nasal decongestant, a. Perrin, Boyd Dempsey, E. Serjeant (auth.) Many chemists and biochemists require to know the ionization constants of organic acids and bases.

This is evident from the Science Citation Index which lists The Determination of Ionization Constants by A. Albert and E. Serjeant () as one of the most widely quoted books in the chemical. Perrin, D.D. Dissociation Constants of Organic Bases in Aqueous Solution; Butterworths: London, UK, [ Google Scholar ] Knjasev, V.

Beiträge zur reaktionskinetischen Untersuchung der säureinduzierten by: 3. All data apply to dilute aqueous solutions and are presented in the form of pKa, which is the negative of the logarithm of the acid dissociation constant Ka.

References 1. Perrin, D. D., Dissociation Constants of Organic Bases in Aqueous Solution, Butterworths, London, ; Supplement, 2. Acids and bases are ubiquitous in chemistry.

Our understanding of them, however, is dominated by their behaviour in water. Transfer to non-aqueous solvents leads to profound changes in acid-base strengths and to the rates and equilibria of many processes: for example, synthetic reactions involving acids, bases and nucleophiles; isolation of pharmaceutical actives through salt.

Introduction to pKaData Limited 1. The conversion of IUPAC's compilations of pKas of organic acids and bases into substructure-searchable data Tony Slater pKaData Limited EuroCUP III Toledo April 2. Dissociation curves of proteins have been extensively used as an analytical tool to provide useful information on the nature and number of the ionic groups in a protein.

Changes in the ionic behavior of these groups have been related to structural and functional features of a large number of biologically important by: 6. Abstract. The survey is dedicated to the critical analysis of different experimental methods of determining the dissociation constants (K a) of organic acids in ages and disadvantages of the contemporary methods of rapid analysis used in Cited by: 8.

Organic electrochemistry: an introduction and a guide. Request This. Title Organic electrochemistry: an introduction and a guide / edited by Henning Lund, Manuel M.

Baizer. Format Book Dissociation constants of organic bases in aqueous solution. Perrin, D. (Douglas Dalzell), Acid dissociation constant explained.

An acid dissociation constant, K a, (also known as acidity constant, or acid-ionization constant) is a quantitative measure of the strength of an acid in is the equilibrium constant for a chemical reaction.

HA => A^- + H^+. known as dissociation in the context of acid–base chemical species HA is an acid that. The Effects of the Medium on Acid and Base Strength - Acids and Bases - Introduction - This book explains the theories and examples of organic chemistry, providing the most comprehensive resource about organic chemistry available.

Readers are guided on planning and execution of multi-step synthetic reactions, with detailed descriptions of all the reactions. Books received Science in Building. By E. Adams, pp.

London: Hutchinson, 18s. Science in Russian Culture. A history to By Alexander Vucinich. A one-pot preparation of pyridyl isothiocyanates (ITCs) from their corresponding amines has been developed.

This method involves aqueous iron(III) chloride-mediated desulfurization of a dithiocarbamate salt that is generated in situ by treatment of an amine with carbon disulfide in the present of DABCO or sodium hydride.

The choice of base is of decisive importance for the Cited by: 5. Based on a comparison of its pK a () (Perrin, ) with that of aniline (pK a = ), it is anticipated that 3,5-dimethylaniline may bind more strongly to clays than to organic matter in soils.

Data on the persistence of 3,5-dimethylaniline in the .Lewis Basicity and Affinity Scales Data and Measurement (e.g. D.D. Perrin, Dissociation Constants of Organic Bases in Aqueous Solution, Butterworths, London,and supplement, ) are therefore extremely useful in analytical, organic and inorganic chemistry and in biochemistry.

Tables of pK BH+ in aqueous solution have been.Book Publishing Center SCIRP also provides a publishing service such as books, conference proceedings, monographs, biographies, thesis as a book and papers in a book, covering multiple areas of expertise. Without limitations on the language or length, many authors greatly approve of our fast and efficient publishing services.

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