Santos, Aone Digerinant VF AT COher 3.\) 1. Sheu by means of A schemas, diagren how Hinsbergs test Hy yeraahodes Pimovy , secondary, cock tehory Aasiwas. Apel 24, 20% Wat, 3° amnes tT Peaeresrgony\ chords 4 excess S%je NACH gow Ov loner Fortrounen pst HOA |reidwe 45% HA CS eee | err Q i Solution 12 amine 2 awming D amine - Is the Masbergs ted Always appraabre ee Compounds Containing, oun Canine Gyo? Ses ace he, Mnwera's Fest vs based Gn the sule Sncumety formedion ak he, reacted Amne with benzene. Afonyt londks Secor up Shoes meteor or Saggerenticdneg parry, secondony od TECHN) Aimints. a Mee gst | stmus acd test — ceachen between omnes and witwis aad, wos used We has 4 vey mak woy 4 Aish ngurstong ber. 9) a5 & 3° asmwgs lov Is ao Longer Counc our Wecanse Wee PRALCK WG YF amns YS A peep coucmoqjen." Referens: 4 Onomapet Feo we | orauec ¢eayslom’: Intreosa.cdl. wmlOrganic Chemistry Laboratory Mar Name: _Claace sentos Date Performed: A ps! 5,201 Groupmate: yen Alpesh, Vian Ton Section: wee EXPERIMENT 15, HINSBERG’S METHOD FOR CHARACTERIZING PRIMARY, SECONDARY AND TERTIARY AMINES. Experimental Results A. Reaction with Hinsberg’s reagent Observation Amine Structure T + CcHsSO2CI +x’s NaOH ayer for earnen nets red Aniline een layer dissolw . lager foreonon, i ve Diethylamine res enn N “n er formasion, Triethylamine aN vy ' Mv > ookernic on Solubility Studies Layer Amine HO 5% HCI Aniline “nselvole \ecaluvle Diethylamine Gluble asolviste Triethylamine jocluble aivble Organic Chemistry Group ¢ Institute of Chemistry © University of the Philippines Diliman