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I TUPAC name of the compound, 1H; aS - C—O is cH, (@)_3,3,3-Trimethyipropanal (b)_ 1,1,-Trimethyl T 412 ipropanal (©) 3,3-Dimethyibutanal (d)_1,1-Dimethylbutanal. 2, The IUPAC name of the compound, CH,-CH, ~ GH CONH, is CH, (@) 2-Ethylbutanamide —(b) 2-Methylbutanamide (©) 1-Amino-2-methylpropane (@) None of these. 3. The TUPAC name of the compound having the structure, HC-(H- CH, CH- CHC) is CH, OH (@) 1-Chloro-4-methythexan-2-al (®) I-Chloro-4-ethylpentan-2-ol ) 1-Chloro-4-methylhexan-2-ol ) 1-Chloro-2-hydroxy-4-methylhexane. TUPAC name of the compound, cH, CH, - (CH,),- CH- C- CH, - CH, is CH, (CH,),CH, (a) 3,4-Dimethyl-3-n-propyinonane (b) 4-Ethyl-4,5-dimethyldecane (c)_ 6,7-Dimethyl-7-n-propyinonane (d) 6,7-Dimethyl-7-ethyldecane. TUPAC name of (C;H,),CHCH,OH is (a) 2-Ethylbutan-1-ol (b) 2-Methyipentan-1-ol (©) 2-Ethylpentan-l-ol (d)_3-Ethylbutan-1-ol. TUPAC name of (CH,);N — C3H; is (a) Dimethylethylamine (b) Dimethylaminometha (c) Dimethylaminoethane (d)_N,N-dimethylethanamine. ‘The TUPAC name of the compound, CHE 6- CHC CH is CH, (a) 2-Methylpent-l-en-4-yne (b)4-Methylpent-4-en-1-yne (c) 2-Methylpent-2-en-4-yne (@)_4-Methylpent-1-yne-4-en. © scanned with OKEN Scanner stu cori is G@) CHLCHCH.CH.cL («cH CHCHECT (©) CHLCHLCHCICH, — «) (CHC Ct 9. TUPAC name of cic, ¢-N, a, (2) Mey --amincpropane (0) Buay2-smine (©) 2Metytaminopeopane (8) None othe above ‘THe IUPAC name fe, on, exycnioncy,-F-08 + ony @) 1 1-Dimeshytutane 12-0 () 2Methylpensne- 2d () #Metyipentane 24! (@)_1.33-Trimetopropane-t 3. 11, TUPAC name ofthe compound, Gig oN NN (8) 1.23-THianopropane @) 3Gyanopentine I Sdinitie (@) 1.23-Cjanopropane (©) Proparesricarbylamine 12, TUPAC name ofthe compound, CH= fH=CH, = C= g a (2) 4Bthylpetan 2-01 (@) 2hylpenan2-01 18 umcomear Yo (2) SMatylhesanol” (0) 2-Meshyheano (©) 2Methyhen-ca-l-l (8) 4Methypent-en-l- sa ne Con 3 ee Brae as 15 ae ant Se 7 @ scum (©) ¢Metiylhex-2-1 () }Metiyexan ZL i we a 1 The compound wit cacao «3 sts cnt? A {i cue-€-€-€-€ us is ot reported i Ny, hs te ue ast Stele (3 Seay methylene © Sopenenare 3 toeane cts CR enpoind () Aliosticmpas Sound (0) Eye ogy, name the loin ound is iu rurac CHCl (©) 2Phenybutane () 2-Cyeloherpbuane (6) 3Phenybatane () }Cjelaheributane b Inthestrture, cH, e-cil-cry -¢ cH, ieee by, Oy thenuner ae (a Overy wo sada on tei () Peri ne ody wd ory {© One pay one onda one ey md weary (© Be pinay, one secondary, en ti ey The sre repeeting erst congo 0 Qo BSS Get, cH=cH~ @ cu=cu—~ cH= cH a = c=0 Scu=cn © scanned with OKEN Scanner esr of nae Cnty enn of hloo-2.2mehybuane is EiretcH vec NCH CL esse ae oreeeeteeten, whch is amaeoatename for methyl propyinetian aber (@) Buune (e) mene @ Powe wich the followings heerxyelic arma species? »U oO Ke “GD ‘y 3 Th IUPAC mame of ar, c= on (0) 2Choo--mthypropane 1») -Choro-2-metylropane {c) 2Chor-2metylpeapane (a) 2-Chor-2-matslbaane 17, The TUPAC name fo, i cayguenecn, ie on On (©) 14-Dinayfbvane13-t (0) &Mepeiane 24k (©) 2Matypentane 24d (3) 13.3eimetyleopene| ti 2. Which merlin TUPAC int cect? (0) Renee (o) Tent 2yne (©) Hexd-yne {@) Nene ofthe. 2%. The crete of CH C= C= CH= CHO * i bw (@)2 Dimetyletane | (2), Teimetyietane (©) foerprepyimtiane —_(@)2-Mslropane. 73. CHCHCH,CHCH = CH)CH.CHCH is (a) SEthnytheptane (0). -Propthex-t-ene {0 dEthengiherane (0) 3-Fthyeaythetane 14. The TUPAC name of CHOCH i G) Methyl eit ether (O) Ethyl meth cher {2 Mathenyethane (8) Ethoxymeans 7S, The IUPAC name of acraldehyde is (2) Prop-2en-Lal (0) Propensaldehye (©) Buvden-tal {€)Propenal “16. The TUPAC name of (CHS):CHCHLCHC is (2) 1-Chloropentane (8) 1-Chloro-3-methsoutane {¢) 2-Methyl3-chloropopane (4) None of the above. 71. Team of cH =GH + cHo NH, (a) 1-Aminoprop-2-2al (0) }Aminoprop-2-enal (©) -Amino-2-formyletiene (4) S-Amino-1-ox e rot nomenclature (TUPAC) for the fttwin a 2. 1 a the 0 lowing represents the nich te aon =P st ener ett— CH?

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