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PN .Chandra Sir PDF
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septual Subjective\Exercise ire organic compounds. found in larger no? eater structure of foll propylidene | ety glycol ! | ithe IUPAC name of ‘tHe : u owing E& sheaTZ eth TUPAC name ob Me following compounds: wi CH, ; c#;-CH,-CH-CH=CH-CH.-cH, ow : it | CH,CH+CH, cH, \| _cu,-CH-CH-CH-cH= Sn cn, gy Hs I cH, Draw the bond line structure,61 (@ 2-Methyl-3-Repjene fi. 7> ee) \ \ ‘ompounds. ENA ae ‘ i Wej jae Rca ene | Abydos eas TUPAC name of the hdripoo and its monochloride, ill {| m the Wren a molecular weight 72 g mol"! has a 2-methyl group. t is ite the gente? Also drawn its bond-line structure? hy | (athe format? 8d Bive TUPAC systematte name of an alkane oreyeloali | | primary hydrogen atpms On EEE Deg at CLASSES 9650289829] | | jname for each : | Va il 14 | | ih {4 ] it ()[G{t, that has only secohdary hydrogen atoms, [What is wrong with the names given for these g ‘om, Pounds Prov; idwhat is the minimum number of ¢; 7 al . (aa branched alkane, bon toms in ) cycle-alkane . | Fi . | ht Give the TUPAC names of the following co: ipounds: ? ot, j 0 nergy cine Gi) CHY(COOH), Gi) CHs—cH CH,CHs 3 Select the correct alternative (ofl < trivival name of the couse 1, The ao ; v @ pyvaldehyde ~“ © a, a, or-trime 7, The common ame, 3, Common name 0 (a) Crotonic acid (c) Propi n aldehyde '@ 4. Commgn name-of the co! mn | CrotoRié acid | Prépion oS) HH 5. "Wtorrect IUPAC lowing coon is: ‘ (©) 1,3, 5-trimethyl cyclobutane | ; The correct statement is about following compound is: i OH it cw’. i, ©) word root i ot is But kK oe (b) 1 | 5-trimethyl eyclopent @) 1,3, 4-trimethyl eyclopentane ethyl cyclop @ 1, |, 4-trimethyl eyclopentane | (b) se¢ondary prefix is cyclo!) | (d) primary prefix is cyclo | {ti | li e cake (aa)WTA T ° | 7. Th freatURAC name i e following compound is: Fada | | il H |i. | CH,-CH-CH,-CHj | | {i | Ane hydroxy cyclohexane) butan-2-ol ) tk 4(2-hydroxy cyclohexalfe) butan-3-ol | (@) we. hydroxy but=1 -y))yclohexane-2-ol | Side ae hydroxy butyl) elohexan-1- | lig htt propane gk ees 2-formyl butanedial in correct IUPAC yl ae enitrile gs 3-dioxo-~ ropent & -methoxy ethanone ‘these Su, a P2*pentenoic acid \yl-2-pentenoic acid -2-pentenoic acid }-amino-4-chloro-2=m i ) tino: -3-chloro-2-met ) nohe of these i 12. | How many carbons are in simplest alkyne having two side chan is ? (a) 5 )6 (©) 7 +, @8 13. [he compound name trichloroethene is : Aig wee (b) Perclen; (c) Westrosol (4) Orlone of unsaturation pol nt in crotonic acid is - “he a ©) A.) © aa @ BB ASSES 9868505852, 9650289829 | PRAGYAN 'CHEMISTRY CL |iit | — ; JUPAC name of com ‘ l pound CH,CH,OCCHICH,CH, is 15. (a) Propyl propanoate (by \\\ | ryl butanoate \ © Propyl butanoate (4) Ethyl propanoate | 16, The IUPAC name of the compound given, teibwis K i (@) Bieyclo [3.2.1] octane (b) Hi sete [3.2.2] octane (©) Spiro [2.2] octane (@None f these i 17. The structure of spiro [3.3] heptane js ethyl) 2-methylhexane iByi-2,5-dimethylpentae i & H i i Gey ) 2fpdimeyipony! ii yi Hl A ADVANCED SERIES (@) 1, I-dimethylpropy! pouund is! i jill shethyl-1-cyelohexen-+ 61 On a Hit} @) 2-methyl-3-cyelohexenol (b) Ff | Hl ©) ‘nydroxy-3-methyl-Feyerohexen® i) AML (é) 2-hydroxyl-1-methyleyelohnen i) | 2. Which compound is tertiary alcohol? ©) al ethyl-l-hexanol | | | (a) 1-propanol @ olfany-neo i | | \ ©) 3-methyl-2-hexanol\ 24,| |In the omenclature of priority order is : (c) C=C<-CH, <-OH (first) : (first) 25.| |C,H,O, represents: @ Anacid only “A. on AY (©) Anketone only ee an ester i cthyst cr) has the 17 re % fmula : APs ., | 3-Butenoic acid (or But-3-enojc acid) is represented as : 1 thio ° ‘ f these | b (a) none o} i mi, ©) Nou © AKu j A | i op (a) -CH, <-OH < C=C (first) | correct code is: \ (@) only 2 and 4 | (b) 1,2 and 4 &) \ f and 4 \ (4) Allofthem | | PRAGYAN|CHEMISTRY CLASSE§ 9868505852, 9650289829 .ee Common name of CH,=CH-CN ig ; 1H (A)acrylonitrile (B) v AB and D a oe © allyl cyanide (D) all 31, Which ofthe following names is cone " ® ey (@) 41sopropyl-3-methyl hexane 2 2 (©) 3lsopropyl-4-methylhexane —(@) Ee rp opropyl pen 32. The correct systematic IUPAC name of th eat pessoa oH le iven compound is CH-E-CH-G-O8 CooHcooH 0 (@ 3-Carboxy-3-hydroxy b (0) 2-Hydroxy propane (©) 3-Hydroxy buta (a) 2-Bis(carbox 33. The IUPAC n ‘| 8 | 36 the correct name feb] =Ois: i \\ Nil) (a) 2-Hydroxy cyclopentanal | \ (b) 2-Formyl-I-hydroxy eyclopentane NM (©) 2-Hydroxy cyclopentane carbaldehyde i i (@) Cyclopentane-2-ol-1-al 1 CH,-CH, \ M\ 37. The name for eS structure HC Con _CHY ig Fo (@) Cyclo hexanoyl chloride (b) Cyelohexane carbony (d) Charo cycloheryL meter | | (©) I-Chlaro cyclohexanal SES A chloride yWAD Wa Ley RY CLASS ETO eer 1, PDas -CH,-COOH || ly id @) 2-Allctoxy ethanoic add (c) 3-Methoxyformyl erhanoic act | ®) 2 -Mnoxyarbony ei jeacid (€) 2-Methoxyformyl acetic aeid | il bon :00H CH, j39.| [The Tupac name of cH IHCHCH— CH—COOH js : ) 2, 435- Hexane tricarbonyli acid he correct IUPAC name i above compoord is : E> : 1 2d acid S (b) 3SMethyl-3-pente | Me OS \ le a Me * TUPAC name ofthe structure is : li] Me k 2,4,5- Triethy1-3-nonene (b) 5,6-Diethyl-3-methyl-4-decene |, viethyl-3-octene ! (4) 3-Ethyl-S-methy!-3-heptene | Il - 0 has the IUPAC name : C eck SevWrngeN CHEMISTRY C LASSE IT EEE Eee TPE LEP)ntanone (0-2-carbethoxy eyclopentanone Hl = 45. a has the IUPAC name ; (a) 3,4-Dimethyl-l-penten-3-ol (b) tenant (©) 2,3-Dimethyl-4-penten-3 i 01 (d) Ni eof the aboye > Hy The IUPAC name of 46. he typ : of ) sp% sp? | lar formula C\HN| arbon atom is given by \ Wi @ 24) \ panos and tertiary alkancls possible " yay ) a, 1 @ 2%a,2 | / Lb is :! | it Wh I Ss, S possibe withthetholestl f (b) 24 Topen-l-amine € (a) amine 51, Which name is correct: , dienal | 1 © mS Ef oO 2 < _— Qa =z il @ “MethyL N-2thyethahanhy a | oN Ethyl i 3-8 foacie i ‘a pe : BOTodobieyeto 2.21) heptane Wot ech yen CH 98685i F previous Years Questions (t| 1 Underlined carbon is sp hybridised in [AIEEE 79 (1) CH,CH=CH, @ CH,CH,-NH, | (3) CH,CONH, (4) CH,CH,CN \\ Which of the following compound has wrot, IUPAC name? (1) CH,CH,-CH,COO-CH,CH, (Ethyl pitancate) @ CH3 aia -CH2 -CHO CHg (3: walt —cH—cH— G) CHG cH, OH CH, (4) Cs GH E—cHe—cH, CH, 0 3, The IUPAC name o} q) isopropyl met ues tie mo) 2. Ndthy!-3-butana (3) 441 net y Voce 2-but 4, The eegeh al “a h (a) aierone! @) dio ow 5. Which one of the fo (1) Acetone (2) cl yhexane 1 \\ ‘| oe 7. The IUPAC name of the compound is ell iyi (1) 6-bromo-2-chlorocyclohexene (2) 3 Hiorho- \.chloroeyelchexene | (3) 1-bromo-3-chlorocyclohexene (4) 2-1 we -6- shorceelo = | 8 The TUPAC name of “VI is \\' tA re (1) 1, I-diethyl-2,2-dimethylpentane (2) 4,4-dimethyl-s, s.dietl peruar (3) 5, 5-diethyl-4, 4-dimethylpentane (4) 3-ethyl-4, 4-dimethylheptane | . a | il PRAGYAN CHEMISTRY| CLASSES | « CY Ye TT EPP LE EEE. a = Tljority for the functional Btoups Ee) ADVANCED-SERIES | The TUPAC name ofthe compousd | | 1) 2-Bpoxy propane és | |@) 1, 2-Oxo propane || Ee peor ony Fo, nclature is TAlERy ri [The correct decreasing ord i of P compounds i in the IUPAC '(1) -COOH, -SO,H, -CON a H,, CHO NH, -6 HO |(2) -SO,H, -COOH, ~ -CONH,» a —C _S0,H, -CONH, (3) -CHO, -COOH, A i |(@ -CONH,, CHO, south itane is: jeegrace mae | | @ 2,2edimethylbutane ethy pro 2 (3) 2:methylbutane | "The IUPAC name CH YH WV ‘C=C-CH,CH, () ¢ ten — ® Cc) hepte! ‘The hydrocarbon th severp|carbon ato! -digpenthyl-3-pentene jimethy|-4-pentene H-CH(CH,), is: 3-Methylbut-I-ene (d) 1-lsopropyl ethylene correct IUPAC Compound is : (urs) | i ul aos CH, cael rc : 5 3 6 ethyl 8-methy! deo ene (b) 5,6-diethyl-3-methyl dec-4-ene (c) oe yi-S-ethyl-3-1 id (d) 2,4,5-triethyl-3-ene i Piet C name of OHCCIE H-CH-CH-CHECH, is: orl CH,CH,CH,CH, | a) 5jVinyloct-3-en-1-al (b) 4-Butylhexa-2,5-dien-1-al nyloct-5-en-8-al (d) 3-Butyihexa-1, 4-dien-8-al reer Ts CHEMISTRY CLASSES 9868505852, 9650289829() 2-Cy4no-4-hydroxy bromo ber @ 64 . The i ma choos? san-2-aldehyde @ a {yl iso butyraldehyde a ound with molecular formula C,H\},, acon wy atoms. The compound is : 0 Q omMm () 4-Bromo-3-cyt heno} (b) 2-bromo-5-hy« oily @ © Chloropheny! keto: 1fTUPAC name of tht ehh ter@utanol and, butanol and b ‘ert-butanol and 1, 1-difhethylethan-l-ol (@ isobutyl alcohol and 2-methylpropan-I-o v Ne / | | 0) alcohols with molécular formula (IT-JEE 2014] EET) ADVANCED SERIES
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