Sintesis Monolauroil Gliserol Secara Selektif Melalui Bahan Antara Solketal

dc.contributor.advisor	Brahmana, Hemat R.
dc.contributor.advisor	Silalahi, Jansen
dc.contributor.advisor	Ginting, Mimpin
dc.contributor.author	Meliala, Immanuel
dc.date.accessioned	2022-11-30T06:34:09Z
dc.date.available	2022-11-30T06:34:09Z
dc.date.issued	1998
dc.identifier.uri	https://repositori.usu.ac.id/handle/123456789/67911
dc.description.abstract	The formation reaction of monolauroyl glycerol has been formed by acetylation of solketal (2,2-dimethyl-1,3-dioxolan-4-methanol) that followed by transesterification with methyl lauric to form lauroyl solketal, then followed by deketalization with HCI 1 N in methanol to form the monoglyceride and result of reaction rendement was 37,31%, based on solketal used. The formation of solketal as a five member ring compound of dioxolan through ketalization of glycerol, has been confirmed by spectral data of FT - IR, 1H - NMR .a nd 13C - NMR.	en_US
dc.language.iso	id	en_US
dc.publisher	Universitas Sumatera Utara	en_US
dc.title	Sintesis Monolauroil Gliserol Secara Selektif Melalui Bahan Antara Solketal	en_US
dc.type	Thesis	en_US
dc.identifier.nim	NIM963106008
dc.identifier.nidn	NIDN8938330021
dc.identifier.nidn	NIDN8909140022
dc.identifier.kodeprodi	KODEPRODI47101#KIMIA
dc.description.pages	97 Halaman	en_US
dc.description.type	Tesis Magister	en_US