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dc.contributor.authorBradley, Lynn M.
dc.contributor.authorHunt, David A.
dc.contributor.authorFitzgerald, Patricia
dc.date.accessioned2018-04-07T16:14:27Z
dc.date.available2018-04-07T16:14:27Z
dc.date.issued1999
dc.identifier.citationFitzgerald, P.; Bradley, L.M.; Hunt, D.A. “Metalation Reaction of 3,5-Dichloro-N-ethylbenzamide,” The College of New Jersey Journal of Student Scholarship, April 1999.en_US
dc.identifier.urihttp://www.tcnj.edu/documents-large/joss/Journal_1999.pdf
dc.description.abstractThe metalation reaction of 3,5-dichloro-Nethylbenzamide was compared with that of 3,5-dichloro-N,N-diethylbenzamide in order to study the effects of regioselectivity and sterics of the functional groups. This is a continuation of the research performed by Demas and Bradley, 1998. The substituted 3,5-dichloro-N-ethylbenzamide was synthesized by reacting the benzamide with a base, sec-butyllithium, followed by the addition of an electrophile, benzyl bromide. All the products were characterized by thin-layer chromatography (TLC), Varian Gemini 300MHz Proton Nuclear Magnetic Resonance (IHNMR), and Perkin Elmer 2000 Fourier Transform Infrared Spectrometer (IR).en_US
dc.description.sponsorshipCollege of New Jersey (Ewing, N.J.). Office of Academic Affairsen_US
dc.language.isoen_USen_US
dc.publisherThe College of New Jerseyen_US
dc.titleMetalation Reaction of 3,5-Dichloro-N-ethylbenzamideen_US
dc.typeArticleen_US
dc.typeTexten_US
prism.publicationNameThe College of New Jersey Journal of Student Scholarship
prism.volume2
prism.publicationDate1999
prism.startingPage77
prism.endingPage82
dc.identifier.handlehttps://dr.tcnj.edu/handle/2900/2234


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