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Organic Chemistry Notes (3 CH)

Organic chemistry short notes and PYQs for NEET and JEE

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63 views44 pages

Organic Chemistry Notes (3 CH)

Organic chemistry short notes and PYQs for NEET and JEE

Uploaded by

anagha a
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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a af wy Be oe 0 3 Ak 2 Pang contin a npon 0 ltr 5p © eR, Ge Bgy SETS (an=a) ee CHA cece, Bp, a ss © coy ep, Bo, Se , ke, (4d=2), (aoe) @ cen Br-cn, SBR OE oO © Rigg) STS ag a Ce aan ee oe ten? a8 So, se We AES, mo“ sae Rr Bk Gye, (Rie ; 2) a @. ts (Sem @, SS pose Ged Ou Compow sh 09,2,5:7 eS OSE os tosoe oes Se) re ‘weavrang tore Han ont ° ‘ronan occurs whth gn Mast abe C - oot an © fa, wie Bere (0) Oo & ‘SH She, me TE ofr stomonypumt stbitne by Back banding Mao -N>-Pho-Aeinp > Harel >t) — @® Ping erpnsion BFP | © Ba Covashin 0 : —(),t—,->-* as won ‘aj & IB se bind tod te 1 Se bend pe ke toad 2 Fede kG seo theo & . oO MOP of Alkane) |. Oo CRY a2. OY © [Foon omaha Haacean at) “eR aes eos) Bone SERENA cy af ‘)r ee = N(R St CE By Sy ty ~ R-& — a +e VO me ey Phot (630) Ra then oO Oey, Oe Gra cake ma pA ey © | Deaton S Satine) (8) OI % hy © 6 * * P oo -B wt LP ge on. o pies _ sie a of [PR Scene RH ~ © ree 508 cf: oO Rea «ye © tate pescforege ew — wah, o dacorinfotion © valle) cnelks) ouclho “Gok, Ose & eos coe 0 ace aoe oF oe Go cal ae |e Lt tos owe @ ested & = 2 ae TS SO oO- . o A & fees an © S 6 a ob a oy! ©G PArnn &. oz geese, Ol Sarma, echoes, O ‘ — © ajo tn ee © ES @ eB. es, oo Le Dae, Jeeatane Rew, Rey aR whoo. Be mek fe matt >a fe © Fo Gripen Progat ERE oyna ars © Fre Hdalis of Code 0 Bec Me Gey Tatton, ALG tno “ep ~ ACK, + FA, yar c® (A, WP oy MOP of Alkane 1. Which one of he flowing alkenes wil eat faster with Hy under nD hydrogenation conditions? (R= alytaubstiuent) ar eq e (caseAIPMT 2005) As an oN on 110. Phenyl magnesium bromide reacts with methanol to ge - @ scar ordre na nacomeyyy~ @ 2 ossurectoene and Mylo oe? Kook? ol oe one oC, © sre pent and Mee © rca tansleand one Chemical prpertien Alkane © [Prateyratan Mans | (Tat 2) RB 4 N-x nay 252 [thein inhaden Sp) feos | oe a ay © +h oy (ein Preis) te Re 5 J tia) (ethow) Be == OI Rob pas Pak Paras fy >> Oy ots >> 1g [ae \ tee Age fines AE Ry TR vorehe to Deeb hy sal gon hi a Vora eee oy SE eg SS ey a ney PY Ce, Ol Ay eH A oO « mee cay ye at os 4o aS ny WE Neg saranda (ony dnt) = 2 coy Sao ae fuk Cy Y= Neg ented nig 3 2 = Nee meectenneted probes (on fodiond dhtbahe, y= @ ae, BH wide pads OD nats eae mais on veegah HOGAN HOEY + Spat & eM Heys cu, eres @ Bean Oo 5 vo te dre age mer in ptt OY Rega eee Rey ali yt Soa late Ge 1 ba Kay Rebs Fy >> GU, > Bry >> Ty Tem RIN ys na ve ie Receine TPE TM Typ THIET MCE WotR ae Loe Yon & DX Bh Kt Oo nest EE > NM, BS we Se CARD a0 fae Ky RES WME OS ea stan (Ge tees] @ Tr flunsnation vet nso @ Tr Sarinakion es duck will be seuided tae b ‘4 0 “feck will be fo i ©_To chlesinaten + Dik ,Paveshons, hididabn lo [Bees for [Crgatgesy * Dead sean RODEN REY Sool #0. The alkane that ives only one mono-clor product on chlorination with Cl, Inpeesence of ditased sumight's 0 (EET (Odshs) 2019) - © 2 2t DA/ +b 3 $ Sas . 0 brie berdice (mop) Ve > eh @ mde Oops > Sey ea eg oh. Jin Ps oa onkeiehe © bby aie. cremeyy Cy-ocm, ~p Geen “ (ge) Phere ena oy Wim Cryo ee (ae 0 Lott pnex a yep Frum gp chai Ret ei Gad ea)” Rew + RecnscuR uk | on 4 @ Rx EE Pe — RR °ck GH ae @ roe B-Ro oS _R— Recheck 7 eam {Sod 9 aaa Coen LS “ne (oe &. \ y aa Paso 2 ~ (mop) © [Deaton of Alabs) |(Rowoval 0) (Ev) © cae WyPa,8 oe @ kayo & Majer pd: - St others, Ber Reon SHEEP —- Ag) fae Reon HEE oie BES |S it.” eS Reams 2 Majer dug. Sh alFOn) > fakes 0 ai cae “lo eu Sy Oe eatin Af! - Che at Af eG ape eter wee ey aaa A Soe oP bf Pike ; oO 28 ste (ea?) Chemical properties of Aken Gy ou’) Nhge tlnntad Cae Seba Ninian eek ee 88 olny (prance RE) © Hydwaeaton Pen (Ahead, Sort) Roney | Cecile Addibon Ren + Bracke © in he > Omratt add? CL meek nebora tatake & Shon and foo) ene EAR wis cheat ® © @ hick dour nut contenn G be AR, So cap vie Nen-clasical & was, (Raat es wean Mh) ow.2 © man! aE (Sasatin Sandoranu. Rom) nwa © Prony, Eronfn EAR Oo EAR vio closvead © Oo ee & oe | ot "e Be oF re By y Ge ® lek, Yash oie renin a © k% 2 8 om omo ge Pac g ce ies Re sani nathete€DC , atOHOTT Oia le Ey nan ST e cara, cm Vey Movkonikey Pals 5B adds whee mane Hon oltre +R addy Where tess Hn athens Waster, Hovieihr Rae) (Yoyshov) © catchy such tot sable © fom, qu. Where Markos Bake ofpeie Oo pon Ge MOF orn, He, a OQ Bom KG Youre XK sh © Wydnobageahon (Fédihon 4 x) (a2) OMe) Rena Reneeey MX mat Relat? aah torte °f pesille) Met Rel BHD @. *- of Robe Lo ‘ ¥ om a “a ty view 2 vam tan me ON “hs rfint hoe, © | Aaa® 45) ie prema q peronds | (ane ute e tide Ryu en pay] Pale toe © wife © Ro + uber @ Renker, + we — ae @ Koma. + ler © Bae > bby os Tobhar 5H) & Pe AG BAe oy Ee - Le ow fer ei YY Add” of Hox in conysohd deve Agia Ob PDS eelc © Kinehed a Woes Ago N conbnlled Rrodud (KP) - » Radic aibvea 2 Meine 1 mate % Produc ucuded Maine 14 al contalled Prudud (TeP) © Prsd Cotobjud ideation (Aad 449) are oO ewe HE Baa fare) Fay Tn Mee Hysuyce HORE ey oNe Reale. RG, Wats eect if (mn ® Oh om foryeranation- Dertwurabie) | (Bax 4% (mle tide. 2raemoume Rafe Se © Heo [RyProrahorcrcdohor) | (eu age) (HR wet), oO Seals ee DHYoAAGME Oo a Petey) QI] Chao Sa bene, CS tale tik Pe neko . Se we pe BNE we ye atm CES hes Bam bn ECO mit cale = MO a, BNSC AD Rem, Rent Ratt, Chesser HESS sayeenpe se eh Sao, OF nee, na hy a dba — a eevee oe C4 Ch Bg ‘ Parag Be re aN Bo ej “ye Ceaeegg bales Oe op DP, Bo By © [brgoten | (ope wir dat) Normal fad (@Eey er eed (#P evn) « Seer ee nbow i 0 Poe Te ae ES Has PS ° fersr oud © wErooe perf aud! , Ue o. ounceus | Oy vd ome ae oa! aye Sud oe frroune aus _ oe 6 a 6 6 Set pbale. 26 Bensireus © (@) perBenaic oud oe @ * bite rvcllon, ersicaud pebeui aud (weton) © [Creates] — oy masse oO & as 4d . cele ae Kop ~w oe "See sore? omen? Som eta or Sen as PAIS Rog! ew { re ole oa Regoors wer o Sots” "0 Bc snctnnnansityentnaactsee (EET 2016, P-) ‘The structure’ is ne aa @ eben, om ewef | euemon) | axsenon) . wo 7 ee #0. HyC= Hew Sem e+ A; A redominany is Sas tn Maton tices A we arb ape poke f ° ——— chy _ @ &4-01-01-cm9 by Cee “[e @ ox or-er-os Phe 40. Which of the following compounds with molecular formuls, Cy yes O acetone on ozonolysis? on My - Seen A © reise yy © cropentane ea dy @ ‘so 2.0tbromide @ 2100 propane © sviromice © rytont/ 1¥Q. Reaction of HBr with propene inthe presence of erode gives 0 (CBSE AtPMT 2008), #Q. When 23-dimethy-2-butanl is heated with cone 0, the ao) obtained is es ae Ceasar 95) SAYS Wag © 2-neyt stone on rr) @ cis and rans somers of 23-cimetyt2-butene va © 2221p 2 tine @ *-c1,-010 @ -o4-04,-5/ 4Q. The alkene R- C4 iy reacts realy with BH, and formed the product 8 ‘which on oxidation with laine 0, produces 0D (case tr 1995) - — Oo covey 8S — oe #0. Produtsf the folowing reaction = ye (CBSE AIPMT 2005) @ 1.010 -cx,1,cH0 a a @ «14.00 -cr,cocn, e@ exo -noocer.en, @ «10001 <0, possiblalkene is om @» mo / Q. In the reaction with HCL an alkene reacts in accordance with the Markownikoy's rule to give a product I-chlor-I-methyleyeohexane. The eor5 oO (case arpa 2015) os 0 Gnd 0086, wo) 1 Elimination of bromine from 2-bromobutane results in the formation of Ln) int 2008 @ prdoinanty ug / Joos ae we Ge © ivoire ofan 2 ete © drcsoinanty 2a © srcninny hte 1 One mole of a symmetrical alkene on ozonolysis gives two moles of alee having a molecular mass of4u, The alkenes 5 {ave 2010 @ vee A @ tue ZS “an 10. ozonolysis of an organic compound produces acetone and a) |mequimolr mistre Wentify rom thefellowingcompounds @ Hence @ 20 @ 212. pemeng A @ 2neiptryemene ateee 2 10, Which compound would pve S-eto-2-methy! hexanal upon ozonolysis? Oo UWEEMain 2015) ot Ge MOP of Alkyne oO D Fam Carbide. Cate tahgo > REC Yat Mae Ugo cot ot 2G, ang co wd. t Cahy Ghy @& [Debgdadalapnaton] {Fre meer) eo TAD batons “PE "1 Bree Bere Prope, He = me UR © bee ier Cag, “ Le eee ' fe 5 det ae Of MOP of Alkyne Oo Chemical paket of Atay boat oO © (Pedic Nobuce bce 28 se! th RPie FH 0 (Se rate nlaasrinn OI oe ie Prkscec, lg cen mie tp i pau ty a aay ne _ Pre Free, bee id > Ate Rg thet (tenon eae Tee Re am eet Oo “ Staessen veer 2019) @ ¥,Po/cinng / @ wm0 He-cec—cH, >< ot @ ver.H0 ote @ nessa, 1 Which of the folowing reagents al beable to dstnguish Between AD (case atPMT 2012) og #9. when acetylene is passed through dil, H,S0, in presence of MSO, oO «compound formed is (CBSE APM 1999) oa @ cH ch fetter noes Coon © cuncte 216» Oaziorn-% 0 ioe eng rectos wiye22 stoner? iaieee 2007 Ae Yar a @Henchanawe, AL ay im 0 0, 2-Hexyne gives trans 2-Hevene on treatment with- em @ P2550, @ uw, @ vm. {WeEMain 2012) ea! 1#Q. The malor organic compound formed bythe reaction of ‘with silver powder is? -ricloroethane they t Ubema, yt Uber, 4 1 , 10. Which one of the fellowing carbonyl compounds CnnDe prepared oO ‘dition of water onan aliyne in the presence of HgSD, 3 H,$0,? [attee 2008), © sncecy Mit. AD MOP of Aromatic Hydrocarbon Cc © Any Br o mite Gin we. GY +L OLY, re on ey oops ° Oso 6 Ge 5 @ & Am MO, E+ tnt (Dempreane) . ® & weone, ) ‘ & HPF mene 7 Theeen Reg me caine ot a J; fy BEM rent GL +H | pay xe o ge a S we “eh sake = a O oO oe See. on = a) ia f Sem ~ 6 *. te OG, py °é € a eh * Elechwpbilic Suanherun Pon (Dulbs-Daler in) Ol 2 - ee Gps Gorn Ch ay. 1 &) BY (hetepnhien o. oe, ST EE Sia, CR pom oe) mae EEL (supe) (Gren op) Tw) a ) we (Freda cap Whe) 2 og SIO a. D wernt at PT eee. we CO re & 2 oO z Set. er Oo “B Le Ries) gBe aren ® Seige So . 5 of’ om parabens ieg) x Ce ee Qe “Sy % 5 sas iy P13) zy x Gummo ld, Cote) or (taae (tothe ead 1, Inthe following reaction H,C- C= CHP 6, the numberof im (6) bond preset in the product Ais Ox @: @« @» oO (NET (odisha) 2019) 40. Which of the following compounds will not undergoes Friedel-Crafts reaction easy? (weer 2013) @ corene @ vee @ Bivctengae~ @ Picne 0 410. Some metadirecting substituents in aromatic substitution are given. OJ ‘one s most deactivating? (weer 2013) @ cen @ -s0 @ -01 O-ny = eos arwr 2009) @ vwe/ @ corcrerzene @© rersptcnonse @ viene 40. Benzene reacts with m-propy! chloride inthe presence of anhydrous AC to we (case arn 1993) @ 2p birodencene 0 @ ero versene @ serexion @© sw-ropp very 0. The reactions to toluene with hin presence of FeCl gives predominantly AIEEE 2007) 0 @ vemyicrorie @ vero coate © ort -crorrse @ 2-ssirtuene 14Q Identify Ain the given chemical reaction. on THEE Mains (26-Feb Shift -2)2021] m Neos « oe eo oo 0 Looe Soni eo eo” 10. For above chemical reactions, identity the corect statement from the 0 following . WeE-Mains (20-July Shit -1)2023]_ 2 Ko. » 10804 Tso). too) Qtr aa? Soa Kerd'w) @ comport servo aan compound '§3Ct © concurs do an compoun is dlarbomic act © compound nd compound are dls @ sr compoun x andcompount re dicarborie acids 'Q. The major product in the following reaction oO {HEE Mains (26-Jun Sit-2)2022 0H9}0K0,H0 a ors i ezr< e> 0. The major product (Pin the reaction 0 Ue ans (20 un su t2022} mw “Benne pmcons a Ree : Choose the correct option forthe following reactions. oO TJEE-Mains(26-Juty-Shina}2022] Off Ro @ ‘20 aetxn arty ation roti: ) sMaoto profits tonto pay © ‘a ath an arora rods @ 2 svertonitov and san Maroy produc 0 4. Identify the correct statement or he below given transformation 110. When enthano is heated with cone H,S0, aga i produced. The compouné go oe cs a ‘ RoR opts fea op oaegea * {1 Mans (uy S-12022) formed when Gio usb teal ico lee sess aon af eG By SAH Ag ag Beyer: eg reagent. {UEE-Mains(25uy Shit-2y20221_ cS) ce ea cS) WN @ ormaisenyte @ A-crjcrcr=c, 8 cascr,ch = cy, Syeet products e Oy EE cyte formic cd t os @ 4-cr,04,04 «crc, B-crcH,aH =, Homann products Orn’ Lie rol on @ A-cihc1,cH,cH1=cH, IE CH, Haman rosy © woe ethan cd © 4-c1a,c1,01- cH, 8-cxcr,cH- cen, saya prods OW) srrooucnow 0 TOPICS to be covered 5 Shon seeps) a Sued Paya ah > Claaieaton of Halostane and Haloarone yen ROX ie Bites > anle Organi Chomlety (oven, lectropil,Nuciophile Leaving Group) setter et OE > Chemical Properties of Haloalkane (SN, SN E>, E,) ate. n@ =" ‘t Thholuottons > Method of Preparation of Haloalkane: oye ie Chas, One, CMT, b tenet Prete eten tigre nan > chemical Properties of Haloarene (ER, SNEA, SNA) fine pom > Physical Properties of Haoakae and Haloaroe > important Pothaiogen compounds > vas Clasifcation of Haloakanes and Haloaenes | Nabe 4 cx bond 0 c 1 Gand tans ones ee Ort eg ten ea Balas Neine teats Casco Oey | _SPbypudasd iF vcd br Rae ey S ath net te ae Sut, Tt St Meee BPR? BSP Shatin tec Boa OH ne te Se? tr end Shh RL CR Br RUCRE Basic Organic Chemistry Subst + Reged Stet Poder Shue Non-pulos seer (ue0) Pulor Soest (440) fae ect 0 ” olan pre Sek rs) oat 9, toning fey (Flos) CVG Pera, Koos de Polov ajwhe Ser (085) O © (me © che e-o% mange Capa fee) © em G-O (Brehune) ‘a o cq @ cw, $-% 50) bell al © oye Sega Oo od OD whe (one 1s) ees 8 Boat Oy i— an (Huth) ae WP Pra (tenn pe pneh) Role of solvent | ( #'+ disselw bre) Oi @) Polow obmhe Schant (pease), © (an flec =P} hehe ise BeB ten gecey + Cohen is ble bad onion hut 7 wnsaisle HB 6 KS) Fs soe © [Res broke Sima] (hyo) BE rac cet ene tn orth oe ae GA) &) eet CY & are ere a Resor Rampant ne Ae, OO fsa ch 0 e Re Spa acne pe ane wR ETRE an. | Se Sekt CORTE. fe Mma. |” cayaibhtaa ere ee meet oon wialnmaa AP Oca acer eh Owns dene ng wp E40 es ress (rms) © Rw omchony © [Re loan) 0 © [Renae BONS Mo Rio | Bo KBr = @ Sy Bons DMP cazh oR, o70e Except | Uses, Re cecare® (gear i) Nypereaa se eS © Re. __ | eee 0 Shae tndond 4 Sprar wich Weaver thy sicher sale compe, Spo She ion [ark Bo Kae oR enn 2 SHA +B se ag Beak ae cS — ens FERRE cngte +S —ersriee Potente Bh, Ba, pencer Pee cent to 9 6 ES 1 Cn “OR oP Sy & Qe ak cot Ky Quy @ caren +e > Opn ND (ongfotren) Brnfils (Meech) ee) ° t . oS bw Hie . a sable (ogy _ opty 0 For (8 CL) Be theineeasing order of aceophicty would be (2007) os @ cea 0D UEE-Mains (26-Jun-hin-2y2022], 0, The correct onder of nucleophilic is @ ow ® 18> 00 e@ ‘SH > nor O Chemical properties of Haloalkanes| ae ogontn Race tony Se m aie on Gene an 1S.) ary (50,99, Sen) Nucleophilic substitution Reaction (NSR) (Sy) 0 ou (nda st) De Cens) © SH (man St rome SR. REG wate") '5N, Reaction] (Unimolecular Nucleophiic substitution Reaction) L a baxeh(e-Aee) «ied ot Meat y a a, fat AC * Coavedeabes SH Beri] | 53 Tf ale ap nme 0 © Mp2 Fase emer Seems) oni | Ras gins Aenea ster @ Padua = Re @ Reo — Ok aa Sees Sere © Rab ysvy oe LEI ers te et on om ai 9 Bt con | Hee if sand oto a ‘a es oo knen Shab DP gine Sgr fa 5 WDE LOH | | D Fosametle coo 4H, 3 3e% 2 Ge netiamy | "f 4 "% ip Ren wek : : 2 Bods rdog Ba | | @ eaercend | Tapa pee 0 Am Ay Oto & hie Or Or ° é & a feo op ae cm Oe) Oy 2 40, InanSt reaction on cial centrestherels @ (100% rcenzaton @ (ernie an ton ngs pari cetion @ 100% retetion @ 100% inversion 0D 0. Which ofthe flowing undergoes nucleophile substton excusvely by SI pecan? {200s} @ rman race 6% @ wopropyictionde -y 8 @ cieviemene OS Ge @ resin Toru DA pny 10, Theoneismost eacve towards Sy 0 1, The increasing order of the reactivity of the fllowing halides for the Sy aoa, reocon Wee Main 20171 @® cucucige gk or ® wns CAGHEH, HOHE wHCO-CHLE & ee @ cucwce @ <0 <0 “ig 4 om © crane p Pp @ oo fa ee @ cue 92, °F eon a » © spe Rade Sng < bgp ts rf@q &_, Size © Sheu Shp | Tee ery Ons & mea ee Drarereerrme trys were ene ier © feta 100 Trvnior © Rats «CRAIC Pe © 07, wer ©) Tew rte vay es) 7 ay @ Ra gq oy 9 & obtade fp 0 Upp im On biRa as Oe rat hy Trier pabek(erT (2) Sete crea o8 Rak ny scapes paaPao pe GC) Fewenatle cad! fits le anced CA) a ees OAK o 3 PAS 4] = “A OH oboe 1D Ugh Ned Sang ee e “© a ea” e. @ Su Se Se Gere nC ites te | o Dd RY nfiiieca ow ® = a oO os en 0 © Unmelerdoy 84 Sa fr Binalecdoy Re Ot Pan @ Ph gor © Peary © Seps 2 @ Sept Dei qema wg ire 2D Rabe 198. Saad BA © Slow Sept © Siw Sipe ory hq TeDaeaOroyr aby curd iy seater @ we @ tae ; a © Ron ~ © Ron K oe eet ee OTF ato Ps some © Poh k(ed © Pah encores eae ‘9 pan Sigh " een @ 0:2 wer Rls Bree, ere’ Reds RookesRUser © Stas = © sates Oh aceremeeee | etiaiomaa! © Rds a © Rusia To (/) aha! east Se es GE ce wowace ansaninace doesnot gve sw eaton — OY] © Reve 0(0r9 ® Rew CEI] Rokk foes fovea + Bus to otha tbe Pay vs wah pistes “Rg. *y. © oan © +x 'SN, Rescon no ven by Folowingsubela Ola EY © oe x = Crelles) oO © roger RAR, A (en) Cy © ofa og © haem x a © etn (109) = (ens) t © aby A (Estes) * X o@t SA tena A (ere) sberaie 3 ay a | ee x * md CP ps x x © Rercneyen foe, (ey) eet A (01) @ ©, e Cre OR VY (ens) Mh. 7 (9) on i oe x x @ reHx- nor nowe @ teix-n,dx-nor-~ © seen ncH.x @ sore ncr-nonx n {AIEEE 2007} 0 #0. Theincorect statement repardingchiaty 6 [weer 2002) @ cic mice shows 0 opti tation. @ sss rections 1:1 mie ttt nates. ‘The product obiained by S42 reaction of haloalkane having chirality at the reactive site shows inversion of coniguration. Q emtoner seperate mir imapsone oes ==, OI a Gia tee ° the ef Se cen pare Ho he) Caged Sp oa, a a, © Rn gq Px wt Manis — |G) Re Rx vie yun R hi a xn Coan) (rape he Cpreprcagint Myeto 0 Gieguanien pe] CO Ren: Ge MB. ow sytye Contain) 3 Je Re sak ony Ae Row 2px Ayig®. Ro-R 42haXL 3 S Er Ren Gq ae Ry | gD e, onic © Pen oe 04 kom Re Gay 228 Oo #2 inans,2 substitution rection ofthe type — Br + C1- Ew — C1 + Br ‘Which one of he lowing asthe highest reacty rate? OGDinw @ Be v 0. which ofthe folowing isleat reactive na miceophie substitution reaction oe @ ee @Qe-c10 cen © cena @ cH. -ceH,01 syns Q 10 Terao ove no om@t ve on eee fal "Q Tetay all halides ae practically inert to substitution by 5,2 mechanism tome tase 2008 Oy @® sarary @ vsisay @ svendne / @ vorcve ter Sy 10. 1n5,2 reactions the correct order of reactivity forthe following compounds? (HE, CH,CHC (CH) CHC and (CH),CCs (VBE Main 2014) © c10,0-0,0-01,010c19,00 ® coxj,c1a- axorc>-cH40> 04,00 © cxe-ccxc10-cxcna>ceH00 © c1a-crava> cmnororiorneg~ Elimination Reaction of Alky! Halide | 0 Cy) & (Elie? Urea) a (Ele Biraulecates) 0 Deryatchaogenston Rescion) (Ey Pon ) (Revaat Hx) (ABP ie Fz) frat gre) Un) ee Tak aa Peel Sand ¥€LTS OSM EB hha” ote @ peeren fp 15 abe Be, Sra! Sake, © &, v We Dh, O Founis oxgeing %~ © Seepage © ok (clover po) (shang bot) © Lyle cbopmetecacdem (Hinthe tabpic ha) ® Seok 5S (mayen) & om aro Aa Ge o Age hose ava lain AS +4 (wasp) (apn (raffomee) @ ro) mee YT fo Be See, fs egies © np atm enc | ME fe (marlon & ateeseens oh (wre 140. Thetimination reaction of2-Bromo pentane tofrm pent-2 ene is [NEET 2022} (A) Fhmination reaction c= (8) (@) Follows Zatsev rule () Dekvdrobalogenatin reaction * (0) Detycration reaction \p W000 ® ® v.00 @ ao @ O.O.0 0 -=D> 0 0. Reactivity order of halides for dehytrohalognation 2002} @ wterasn-nert @ vrrwer-arng/ @ brr-aon-teonr @ Bekok BroR- 0, Elimination of bromine from 2-bromabutane results inthe formation of— O cased) @ pron -bens 6 ae @ ‘equimolar mixture of 1 and 2-butene = Cast fan © rein teye ® Pretominanty 1-butene (eens) (Pm 479 (fe) (Pa) Seow Og vafeatens DeeK + Nets nee 2 * Satae® Toy, © S41 64} Lt Otay th *eih) SE cae i. &O 072, m2 © hor (sryrohaapeatonReaten) (€, Matron) (Ea) (Ret sae) 0 a eset A AP eA Ay *b. DE a i oe eee [as J spy . forhar & ie BAS ws a, ne Kem ) oGas Ged = Dayaotonqtenmecion (Fre Rn) (Femeigne) A Fave, SOF 1 Bh, ae BL Sy A Cond? fo fen “Ri | © pow tot Sota Bar Sy © ogee (my! * Mee dg wail be dood ys DY EADY Me estan me 4 thes "TS ced Ne on e iG KR, sees E US onsew se RR fe Ak An ye oyt My, E Reaction Jou epg Sihahasis —> SMe gine ee Att Bakes Comparison between S,/ S./6IE, © yom — Alang SH @ Rem - + 554, (Re ag {og an syn 22, neem Ay > mers San fated pce et ln nr] eS MS) [iyo tor moe Roce} Or jan scmliesgenpane \ K rine > S6, (Besag) +E, [Soagbetat p) 0 Se 0 @ Ron a feesay state] My 10.2 - Srompentane is heated wih plassum eben neta The mar prod cael 1199 eles NN ah @ 2 soopeniane ¥ — @ Petes -1 we, @ ee / (ots © wre? * FEE i A CSSA Yao AY o Ola Mitel ne cre? @ (hana cannes nd on ein @ tno 2s mtrstan sl) watery ~ © osetia) nd) are sweatin eons @ ssrs0n 2) an) ato recto 0 Consider the reaction sequence given blow: ‘Which ofthe aiowing statements is rue O [WEEMain Online 2020) Pet ea! eran ne! None (Changing the concentration of base wil haven effect on reaction (A) Doubling the concentration of base wil double the rate ofboth the reactions Changing the concentration of base wil have na effect on reaction (8) 8, Bat nave no effect on reaction (8) MQ, Inthe given reaction 3-Brome-22-dimethy butane SAO 4 Product Als ‘ete 0D WEE Mains (20-Jly Shit “ as @ 2 ir0733-amevyt butane @ 20 22-tmeiytbaang// * sue « @ 28200:32 eto. Reaction with Metal © [Wows Be Rix we RR Gwe e “Tova Tes oa Oo Geto Rage) Reap (Opis Cnt) Rx Mo Reg Bye Bee Daye = con ow a oa re #0. Which ofthe folowing kane cannot be madein god yell by Wars ection? "0 romo--chloroyeabutane when treated with tw equivalents of Nain he eg ew eon eg A >s en ® e q Q ee = = Oo TWOP of Haloakane oO —— on a Fear yeovkan, Frere Blaha Feves Aly? habe CY wgeon ia fate Hip 1 Photohalogenation of Alkane Ren RGAE ROr how BO YX 7 Baw er CAS YS py & mo Ot 0. Which branched chain isomer ofthe hydrocarbon with molecular mass 724" _ivesonly one isomer of mono substituted aly halide 7 @ ereane A @ wevresane eae a “os bo%, ee m 2012] @ ier inotcinide o ey opens 8,

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