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dc.contributor.authorNjue, Wilson M
dc.date.accessioned2013-09-26T07:22:05Z
dc.date.available2013-09-26T07:22:05Z
dc.date.issued1980
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/56736
dc.description.abstractIn the leactiol1 of arylacetic acids with alkaline sodium hyp och Lorit e it has been shown t.hat the nature of the products depends Oil the substit.uents on the ring. Hhen electron atlac- ling groups arc present. the products arc the next. lower aldehyde and/or carboxylic. acid: the type of product. being det.ermined by the experirnen t aL cond i t i.ons , Whp.n electron releasing groups are present the ring is activated towards substitution by electrop~iJic chlorine to give ch10ro- and dichloro derivatives. In phenylacetic acid itself, contrary to a previous report, we have shown that both oxidat.ion/cleu:rhoxylation and chlorine substitution of the ring pay take place. PYlidyl acetic acids behave in a similar fashion t.o benze~e deriva t ive s bearing e l ec t r on T",itbd~~±-ng groups.en
dc.language.isoenen
dc.titleSome Further Fractions Of Arylacetic Acids And Related Compounds With Sodium Hypochloriteen
dc.typeThesisen
local.publisherDepartment of Chemistryen


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