Edinburgh Research Archive

Influence of substitution in the benzene ring on optical activity : menthyl esters of di-methylamino, amino, and hydroxy benzoic acids and the octyl phthalates

dc.contributor.author
MacGillivray, William Eoghan.
en
dc.date.accessioned
2018-01-31T11:47:25Z
dc.date.available
2018-01-31T11:47:25Z
dc.date.issued
1928
dc.description.abstract
en
dc.description.abstract
1. The theory of General Polarity has been applied to the effect of ionisable complexes on the rotatory power of optically active benzoates and holds for ortho,di-methylamino, hydroxy and carboxy esters.
en
dc.description.abstract
2. The ortho amino ester is a notable exception, which has been explained in view of recent work by Sidgwick on co-ordination compounds, and confirmed by evidence of boiling points and solubilities.
en
dc.description.abstract
3. The exceptionally high value for the union-ised ortho hydroxy ester has also been explained by Sidgwick's work.
en
dc.description.abstract
4. The meta and para compounds are unaffected by ionisation except in the case of the hydroxy compounds,the changes in which are governed by the general polar effect.
en
dc.description.abstract
5. The concentration of the solution has a very marked effect on the rotatory power of the ionised Sodium sec-β-octyl phthalate. A very rapid drop in rotation accompanied by an inversion in sign taking place as the concentration rises. No satisfactory explanation can be advanced to account for this peculiarity.
en
dc.identifier.uri
http://hdl.handle.net/1842/28478
dc.publisher
The University of Edinburgh
en
dc.relation.ispartof
Annexe Thesis Digitisation Project 2017 Block 16
en
dc.relation.isreferencedby
Already catalogued
en
dc.title
Influence of substitution in the benzene ring on optical activity : menthyl esters of di-methylamino, amino, and hydroxy benzoic acids and the octyl phthalates
en
dc.type
Thesis or Dissertation
en
dc.type.qualificationlevel
en
dc.type.qualificationname
PhD Doctor of Philosophy
en

Files

Original bundle

Now showing 1 - 1 of 1
Name:
MacGillivrayWE_1928redux.pdf
Size:
8.79 MB
Format:
Adobe Portable Document Format

This item appears in the following Collection(s)