1. The document reports the results of several experiments involving the functional group analysis of organic compounds using different reagents. Observations such as color changes or precipitate formations are recorded.
2. Based on the observations, inferences are made about the presence of functional groups like alcohols, aldehydes, acids, bases, etc. in the compounds. The positive tests confirm the presence of the functional groups.
3. A total of 10 experiments are described involving reagents like bromine water, sodium nitroprusside, Tollens' reagent, etc. to detect different functional groups like alcohols, aldehydes, acids, amines in organic samples.
1. The document reports the results of several experiments involving the functional group analysis of organic compounds using different reagents. Observations such as color changes or precipitate formations are recorded.
2. Based on the observations, inferences are made about the presence of functional groups like alcohols, aldehydes, acids, bases, etc. in the compounds. The positive tests confirm the presence of the functional groups.
3. A total of 10 experiments are described involving reagents like bromine water, sodium nitroprusside, Tollens' reagent, etc. to detect different functional groups like alcohols, aldehydes, acids, amines in organic samples.
1. The document reports the results of several experiments involving the functional group analysis of organic compounds using different reagents. Observations such as color changes or precipitate formations are recorded.
2. Based on the observations, inferences are made about the presence of functional groups like alcohols, aldehydes, acids, bases, etc. in the compounds. The positive tests confirm the presence of the functional groups.
3. A total of 10 experiments are described involving reagents like bromine water, sodium nitroprusside, Tollens' reagent, etc. to detect different functional groups like alcohols, aldehydes, acids, amines in organic samples.
S.NO EXPERIMENT OBSERVATION INFERENCE ALM: do outLct Kncaonal Gsoup UKuUA iUA orgauc CompOun d LLsEk7 un &aaur ao on: BrO mint w atun LSO, wn PJu&uNe ak wnsaLYauo A dd a u drops o RAdclLS h bown colo us congirmA was dLoLowusL cOm O u n dd ) Bayns RiagANE A d d a fuw dops o4t RAE colo wn was cold oiuc EMn Oy 0o cco lowussd is cOirmLd U i w n compound TLSC fon olco hol S: EStUT Addt d m acoe acue A U u y Oao w a conc obsuwed Duou is naicatid and a ( oliops Of HS, compoun a GaJ7 mua Ct Ammoum Nioat pink Jud cotouurraaon lcoAAwC Atew arrops Oy cwu PJusn a o um mONntm u r u Kiagint w as ob U u L d congmud is addua co m l of 9iun compo wnt and 6 hak w . 1D 2,4-DN TLSC An arargi CTH Stallun psuunu of co76o) Addua 2 , 4 - ONP aD K P u i p i t a t i s obcainnat anet shaks JLctid Spitit 2) 2) Fahiine s TiSC Addic quot voumus A JudciSh 6Jrown A d 6s prucpLtot was obcainna U o u p d S Lekrmael O4 FLhiings an SoCuon bo conpouno and wosmuLcl DATE EX. NO: S.NO EXPERIMENT OBSERVATION INFERENCE 3) TolLnsTSC, Addic To l n [ Jua9nT w_ mirroa was RUSna a alduiy aic in 9 i u n Comooun d obuusd on Twals TO up i s co nrmia aan d wonmud i n a hott watu7 bathb isso W O. 5ml or o.59 pink, JLd an Nagunrapru ce Ot aldÁgeac. J u U 0mpound in o o w T ouon was oLp L e _ c o g rmial O4 I mi 0f SckiKbS UaaNs 06toinca was addiot in) Tase on kusnLS 2,4- DNP TLSC. O A Hddud 2,4- DNP An OnangL Cystailinn Aruun can6ony_ ivn compound i n puapitau wosformLa roup s inclicoa Juapua spirie anc is Shakn 2) So dium Niroprustdu D Adud a kew dops R Coloun ocon wa ob&uwLdl o So dium bropJusLdL to C h 8 i o n compound and add Nao H druop u&L 3) m- Oinibro bunau ust Vi o uet cOLO wr anon wa Addid N- diiobs B Oon d diuu So uuuo n ot obcaino NaoHCO Ou compOunc (IV) S E ton canbory ic acid 1) iouuS TSt BCuu L m u s aU7nS S ubston i s acictuc AddOL a m O o buu tmus Soua0n i n naC ChA compOunod 2) ESCn SC J uy o oLowT was uSLn a canbouc Addi a [ml og lOAO aciel i s iLicobLa an d fcu vsps f conc. C mpouno DATE EX. NO S.NO EXPERIMENT OBSERVATION INFERENCE 3) SoticLm&iccnbon ac s l Addio a u ainch of| SoduLm aicos bon C C obtoind CRL compouna Lnicallo (V LLst o a AminLs LiCus LSC: Aallda w cUrops Rid i o n u s UTnS b u u J L Su6&ta JTed u c m u s C0 iu b asi c un n cutw CO Mpound 2) Sowbiigy TusC Addid ol, H J Substanu dissousJ Subsonu is baSi in n acUu aiuun ompouna 3) A20 ay LsC ssou OLun An an angi duL was CompOun d in 2m/ of coC. H c Obtoins amin i s cDirmue ie cnd adc Cawmag ond cool ie i n NaN O vi Tcso tan Phunolss I) icmus TLstt: Adodiot o e w duOps B e ioms bou s ud 6 o ubion ws b uu uamus So uuuon aciaio in naber Comp Ound 2.) Narur al Fed LS C, Addsd a uw drop s of AUioG CoUo oiadon weusPusnu aA PALnouC aL O btainLd SubsOna. RisuE: I n c a o n at aoup B a i n com poeunot zoun and uporua
Recent Advances in Analytical Spectroscopy: Proceedings of the 9th International Conference on Atomic Spectroscopy and 22nd Colloquium Spectroscopicum Internationale, Tokyo, Japan, 4-8 September 1981