| dc.contributor.author | Numbers, Annie Hutton | en |
| dc.date.accessioned | 2018-01-31T11:34:09Z | |
| dc.date.available | 2018-01-31T11:34:09Z | |
| dc.date.issued | 1926 | en |
| dc.identifier.uri | http://hdl.handle.net/1842/27132 | |
| dc.description.abstract | The investigation of a number of optically activeoctyl esters of 0-, m-, and p- substituted benzoicacids reveals a regularity in the influence of substituents in the ortho-position. | en |
| dc.description.abstract | The m-directive or positive nitro and carboxyl groups increase the rotation of octyl benzoate, whereas the o- and p~ directive or negative methoxy and chloro groups decrease the rotation. Further, the relative influence of these groups with respect to hydrogen is in agreement with their relative influence
on the rotation of menthyl benzoate and with the irrelative influence on the substitution of benzene. | en |
| dc.publisher | The University of Edinburgh | en |
| dc.relation.isreferencedby | Already catalogued | en |
| dc.subject | Annexe Thesis Digitisation Project 2017 Block 16 | en |
| dc.title | The Influence of substituents on the optical rotatory power of organic compounds: the isomeric methoxy and nitro-benzoic esters of active secondary β-octyl alcohol | en |
| dc.type | Thesis or Dissertation | en |
| dc.type.qualificationlevel | | en |
| dc.type.qualificationname | PhD Doctor of Philosophy | en |
