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dc.contributor.author이도자-
dc.creator이도자-
dc.date.accessioned2016-08-26T11:08:23Z-
dc.date.available2016-08-26T11:08:23Z-
dc.date.issued1969-
dc.identifier.otherOAK-000000057974-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/202658-
dc.identifier.urihttp://dcollection.ewha.ac.kr/jsp/common/DcLoOrgPer.jsp?sItemId=000000057974-
dc.description.abstractThe experiment was intended to use β-Naphthol which was known as antiseptic sterilizer and try some coupling reactions with diazonium salts of several primary aromatic amine compounds. In these reachions, azo compounds were not appeared as same color, for example semicarbazide was appeared as white or yellow. But generally, their colors were between orange and dark red. Some resiniferous substances being occured in β-Naphthoxy acetic acid, an experimentalist could not obtain satisfactory result. Generally, all of azo compound formations were coincided with theory and yield was good, too.-
dc.description.tableofcontents目次 = 1 Ⅰ. Abstract = 2 Ⅱ. 序論 = 3 Ⅲ. 實驗 = 5 1. 芳香族 第一級 Amine의 合成 = 5 (1) P-Iodoaniline = 5 (2) Anthranilic acid = 6 (3) Sulfanilic acid = 8 2. 芳香族 第一級 Amine의 Diagotigation = 9 3. 芳香族 第一級 Amine의 Diago化 物質과 β-Naphthol과의 Coupling = 9 Ⅳ. 結果 및 考察 = 12 Ⅴ. 結論 = 16 參考文獻 = 18-
dc.formatapplication/pdf-
dc.format.extent580372 bytes-
dc.languagekor-
dc.publisher이화여자대학교 대학원-
dc.titleNaphthalene 誘導體와 Diazo 化合物과의 Coupling 反應에 관한 硏究-
dc.typeMaster's Thesis-
dc.format.page19 p.-
dc.identifier.thesisdegreeMaster-
dc.identifier.major대학원 약학과-
dc.date.awarded1969. 2-
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