Show simple item record

dc.contributor.authorNumbers, Annie Huttonen
dc.date.accessioned2018-01-31T11:34:09Z
dc.date.available2018-01-31T11:34:09Z
dc.date.issued1926en
dc.identifier.urihttp://hdl.handle.net/1842/27132
dc.description.abstractThe 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.abstractThe 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.publisherThe University of Edinburghen
dc.relation.isreferencedbyAlready catalogueden
dc.subjectAnnexe Thesis Digitisation Project 2017 Block 16en
dc.titleThe Influence of substituents on the optical rotatory power of organic compounds: the isomeric methoxy and nitro-benzoic esters of active secondary β-octyl alcoholen
dc.typeThesis or Dissertationen
dc.type.qualificationlevelen
dc.type.qualificationnamePhD Doctor of Philosophyen


Files in this item

This item appears in the following Collection(s)

Show simple item record