Rotatory Power of optically active Benzoic Esters containing Ionisable ortho-substituents.
dc.contributor.author
Hill, John M.
en
dc.date.accessioned
2012-12-06T13:53:17Z
dc.date.available
2012-12-06T13:53:17Z
dc.date.issued
1931
dc.description.abstract
Among the many and varied fields of present
day chemistry, that of optical activity occupies a not unimportant position. The rotatory powers of the alkali and
ammonium salts of d-sec-βoctyl hydrogen phthalate
have been studied in alcoholic and aqueous solution.
The rotations of the salts were found to be in the order
H > Li > NH4 > Na > K > Rb. It has been concluded that the variation
of the molecular rotation of the salts with concentration may be explained by assuming changes in the degree of dissociation of the electrolytes and a
deforming influence of the cations on the optically active anions. The effect of the addition of inorganic salts
of various valence types to 0.2 M aqueous solutions of d-sec-β-octyl sodium phthalate has been investigated. The series for the depressive influence of the
alkali and ammonium chlorides on the rotatory power
of the optically active electrolyte is Cs+> Rb+> K+> Na+> NH4+> Li+. The corresponding series for the divalent chlorides is Ba++> Sr++> Ca++> Mg++. It is concluded that the observed effects may be
attributed mainly to a deforming influence of the positive ion on the optically active negative ion,
the explanation involving a consideration of the
ionic radii. It is worthy of comment that the above
results have been obtained by use of a carboxylic
acid containing no hydroxyl group.
en
dc.identifier.uri
http://hdl.handle.net/1842/6532
dc.language.iso
en
dc.publisher
The University of Edinburgh
en
dc.subject
optically active electrolyte
en
dc.subject
rotatory power
en
dc.title
Rotatory Power of optically active Benzoic Esters containing Ionisable ortho-substituents.
en
dc.type
Thesis or Dissertation
en
dc.type.qualificationlevel
Doctoral
en
dc.type.qualificationname
PhD Doctor of Philosophy
en
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