Alkyl and aryl halogen notes, Study notes of Inorganic Chemistry

Alkyl and Aryl Halides – Complete NEET Chemistry Notes | Reactions, Mechanisms & Important Questions These notes provide a complete and easy-to-understand explanation of the Alkyl and Aryl Halides chapter from Organic Chemistry. It covers important topics such as structure, nomenclature, methods of preparation, physical and chemical properties, SN1 and SN2 reaction mechanisms, elimination reactions, and important conversions. The notes also include NEET important reactions, previous year questions (PYQs), short tricks, and quick revision points to help students strengthen their concepts and improve exam preparation. These notes are highly useful for NEET, JEE, and Class 12 Chemistry students who want clear concepts, quick revision, and better problem-solving practice in Organic Chemistry.

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2025/2026

Available from 03/13/2026

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PRE Pl R—H + Xp 09 a x + Hx Xa > 2x Fa) ch) 6) | R-H + XR + HX | an TT R + X—X—>RK + XK _ (Bq ydichabogenation 2 alkems SYp> R—-cH= (Hy + Hx ——> R— CH— CHs x x4 R-CH = cH, + Hoy [92 ——> R-cH, cH, BY _* (Coy bilepemation of alkenes p> 64 _t = a + Wrr[coly > a a By 1S (( By suaetion ata Hox QYp R-CH= CH, + HOX——> R — CH — CHe OH x 6. (( by rwadhon of %2/10 Xp CHy =CH —CHs + Kah” ——> cH, = cH — cH, —x i) Hy = CH — CH, + NBS ———-> cH, = cH — CHy — By : > (CH iailogre Tap D> R=¢ Sty + Hx —__s e—loen, ! > Mp aap cae yx, we, f er low temp, y \ x \ fo. se ae SP re CR a @ + Kaffe its, * Halloasmabion rho B hybogem inctopic tphect. TCH CDy (Rete) | \ ~ b= 0~ ty Ba] ccly —"—> R — By + Moy — cop n i) Sea GTS, Prsfecl apn ly ef bn emake tll, sacs ty fa with nae al _ a BREA EE + me + Rte + ye R. + Ba B41 ———> R-BH + Oy. Aye + Oe ——. Aagy | o Mi R- c— o+p—_s a > _sinteltein pando RF + Nal] Aectowe ——_s pT + Nae RA + Nar] Aeflom gp oy Nae! Mae > Neel > NiO : R-BH * Naz | freitong Se Rae Noy Q Tonte ame only not Ly rdluble in aeiting lsccunne it ir covaluit. All othe cue jonie ound not aoluble. ) only. wvolost wt aohuble in organic advent, j-e — oxdlene wae yn. a _O™ “aha — ae liad a o oF ay = CH — CHy ——— CH=CH — ey — 7 wet ei CH. = cH — 2— cH “Hs ———> tra = cH— eH, — Q— ScH = CH — cH, I A crs —y —CHg-L : 7 ayes de alo as 2 t~ ae | c = . We=en — cys —_, CHa = CH — cH, — 7 — pa - Oh =o — any eelyo one en ot . oho F i ce 7 Un = CH — cH, — y CHa + |] Naz/ hedtone . \ ) > m1 a > Q—cH—cH — a —d + Naz] Realong —s fl — CH=CH, — cH, — Z / BA—CH= CH— CH, —F + Nax/ fetliwe —> Q4—cH= cH, chy— I 7 19.9 Thir sunilion Jr wed btcane or (odenalion Sy sunenrible , Jk iy difficult cto prupare iodine prroduclar, By SWARTS Reaction Rody tye tig > RF + Agel R- BA + tye ov SR "a | mp RvTY MP us pe + fa T < ovby oiler flunside in poluble im Wild} ond oftwur ort prucipitatid . oo only MF Je flowmed. ; set of th dain Ss at flciy yy 7 eMownier ome vse. wat Jt to forny uno puoduaby : uc a ct \ chek 7 Cys Cy Cy" ne gees ae TH cH=tH~ CH, - S Ha By CHy- F a s Hdd ta \ CH= iia a-T AOF @ ————> @ By cH y= cH —CH,—F £ L q Bs Nueleophilicity MM prahie — PG Er UME a= . Fn Pprotio = a> a BH Ee SO, 92 Woe palloing sontlon —» Rcd + KF/ome ——__sR fF + Kee Apsecchis. Fr mort wucloophilis CHa By CHF they el We Lam aloo ue Ket] DME te saplack b12r falc kaa] DMP fon T but Hun iv ro mining of Kx] DMF. A { \ sith R-OW + KX—__s ng. HX leaning, atu HO i-e poutuadl psup ener home good Loan) aa) 7 TONING group Jy oH whith Jy mat good. Poucen ty With Rox to x Aa tht sanction, ro "fawidevd suastinn Lars kry HgP0 Pe R- OH ——=» py : - SKI + HsPo R-on 4, NR CH2-OH \ieeemaameai CH. aa 4 He Po 7 R-oH KEENE 8 — cHcOH = H O 20) eton/es vn —* . NR H a FOR PRIMARY ALCOHOLS ra RCH, — oH pe oy og ey D0 R Cbx j +r 0 aa : Koy, Be NL —_—_—_—————_—— ee Oe pny yes x —"t, ———== x Aj 2 < w rar Rake < [ror] [Hx] Tt iv ubstitilion nucleophile bimolecular (sna) Ml prumanay dbeohols undies nucleophile aubestation by SNo wiehonlen . Ts te inlotmedicls wo Stosromarmtsh . Rate 7 duudly proportional to vovadi Ts. Mant droridel ideal toon scent ae under Hal svaition ok ne faotist sali Seeen & Tati, abroddy do wat wndungn dab meclominy peimasuy wedge fat. 1 tow “woah oul ya Poe bocmeling, mn p vaxbon T, cvonding 9 Te T Hemer suite wanpenii fo aleolol appt to be primo bat deo nat unduigo tr widow . q HA Og tHe CH3 Hp, CHa CHeOH ——> CHyCHa CHa CH. OH, /*—> CHgtha CHatty—x Pigg tH on CH Ai: (Sore > tate nat undango SNo Wochamirny (( Se Paste aalvent > HL 7 4H > Hel > He Beaune HT far arongert vid 2 1° formed be ational wuelooriibe { Molvent. Prilie- im pouatue MECHANISM FOR 2&3 ALCOHOLS = ‘Ae & x ) Ro € OH + MX SS ete a> Be RT Ry—c— Ro Rs Ro x Thuy, wndurgo log SNy wuchowuiny lxcaung conbouition Jr wart. stable im 9 4% cleohal ovorall odo. \teitbuay y Stomdany > Pula | | a cats + 7__,-¢ 2 ¢ —+ © 4 aH x | (cimincition) ELimivelion ater ot higly Timpurolure Addition ocew ot Low Simprrotioe Jubstitatin oceutr of Cony. Fomyporaluse AW = ahs T as at luigh Soinp , bh aq -NavH (basic nating). Aimilay lo 09. kono Kon. ecm Ome “Oe a 7 ; oACle ae nF * ellng ge asasd +NlaoH ~ WuRTz Reaction QR —XK+ No—sRR ©. R-AK +e —S PO + KO (tuduchion) 1@ RM +e x-—R—-R + xe (aubiti bitin ) Pool from alkanoty. Rul? + R-x——9ReR, _ SF \ . ZINS. ; (Pp BLAYLATION a ples - fal 7 CH= CH ——_, Reon CH=CH + NaNH,—>CH=c! Nats CH= C-CHy+ atm CH= C Nat + cHycHek——>cH=c— CH CHs oO NaS CO xgt + 2¢Hscl—>ecHg—c Sc — Cth, REACTION WITH NacN] Ken Reehaek 6 Nae > RH, SHaCHeX + NacN—scHycH, CN Y ASenaseal Gent oe ECHANISM _ x gd . = v8) 9 FA NH—> RC. in, ate VS CH3CHs ——» Auechnie arid a Hove’ —cHg — CHa — cooH —7 cg th, ant CH =a, BY—CHa— chy — By 28 CN cH cHa—CN VHe4 = QI CHytHs ——> HyN CH, CHa CH cH y— NH HOC — CHy—CH,— Coon _ Hal Nem cng CHy—en tals yy — oy, CHy— Ni CHy~— CooH OQ- a Prom aedtie arid Rome oP — N= 0 ——>R—cH,— 0 —N=0 >) O° ta Abvomaey nudivophitt CHy CHB + Nanoy ———_s, cHgeH, OND (ctoyl vious) nia cHy-ONO co. OO an Os REACTION WITH Agnes ° 0 co) R — chy <—in7 ——> Roch —N =O—> R- cH — P7 No en sino \ 0? x *t ("otkena R-O Not + Riayat a Re CHe — Ry . : The prupantibion of otherury from foodiumn obkeatle by sansfuim vith primary obkyt walide fr called vailliamoon's axyn-thur 6 el anata trp cs OHA” Chg cris oh CH 0 Cy CHs + CH=CH, + CHa CH CH, 07 Not + Clgcl ———9 cH cH, OCH, (lig product) Hemeg , Avesnd method should be ured. 7 @ CHa CH) O CHy CH, CHe CHs CHO Ni tip MAO NOt eWgcHs CH2cl ——> cHycH, o CHs CHa OHS + CHZCH,0H + CH=CH OY; med CH3CH2CH20” Nat cl tp + CHycHacl > CHyCH2 CHO CH, CH + CHSCs CHaOH + CHECH, “ p=E i i ' eS CH3CH, O—C — cH, mmo | ots CH, CH4—c — O7 Rat CP cu, 1 OT Nat + CHa CH > SHg—C — OCH, CHy > CHs CHs CH ons ~ CHs CHLO Ni \ ie : WP cts M,0 Na i d —, CH, CH, OH +CHa=e —CHs . Hore onli iF retuod qhovtel be une, ESF csc 0 ZS ~ ea —s ~ O-C . 7 \ Peoticas 7 aa lis CHACH.O-Nat io - ( y) (1 CH,ONat +. |] —— > NR sf / Vv S + - Not CHs = + conf d = ©) cHy—6 — cy : ts a i's SSP How prapane Dee . i on cH, ie “s ts 3 = CH + Ha (ococy —> cHs—g — CH. = Hs ashy’ cH, ° 3 : CHy—F— CH, + Phono ——> one Sits fo) CHs ~~ HO—CHy CHy chy cHy~el a 7 Q . arid . “sor _ REAC TON r KsH OC W R-cHy-A + gy ~———> h-cha— SH + Rx : (ncn) Poe lxomelai Twetane of g canbon sulle of sumtin ducnsanor aw Ts Te umstable dugto cHondi amd lucomoy difhiodt to form. — _ CHa — CO — CHo-X CHs-X CHa CHE X D> CHy i CHa —% S 4 i, Pa CHs cH, VS 2 Rate of. ssactiom CHs 4 = a cHEc «cu,— aA > CH=CH & CHa el cH — CH > CHa ch Rae of si Sw rose Sy I bot c= e i withanancing quoup Cund, Lemet tha 5 . carbon dis mask e- deficient” +0 z” Glock, He mart e defi cheut cascbon. Hence Subla of Snip sandhion t. ia} H 2° saan Th CH CH, CHo¢] HO™ 255 » i accagh a“ hl ee . (12ke out) ni Most vrovding Ts unatable AN a7" (veowded) CHa =CH — cH, — cll = 4 Sr recovers (Wall) Low tenella Ts sslalively Aboble (Pale) Ts Nou able er condi H H eas Homo 4 (ca ean Ho. oe nal | i , é i H” “Sy r H > 3 Anoitt e» lam aon : CHa, CH CHp— oh CH, =CH— cH, ~ cf cHEe — en, cH ) ) ; bond tremeth artes , weak bend beak onnily 20 st of JD tow bso Pit bond adfocunt Sabo nda, nop uid omd P orbital 4 coxbery unde na- SNo Lntoruct (delocalise) which Alabiliae tw Ts formed Ses (CH =cclgel > Cla =CH—cHy—e] > CHa CH, CH, ol (oe ‘le ie L Ly = Cy Cr" a Z chads on em debiciont Gy Bond aowath | ya = nj weak tab » 0 in ety do bunk. — GP Lhoy 39 ahuudvg dt I te planar. vo wand vconding Jy 2 (EY) jaunt double bond To canton vandungating. sip sancbion Henet s0fle mort or TS bs atahle. Sooo timo word thaw it. RSF cUatt OX AD, CHO CH whom wok dy HO,eyonred . CHaCH,O how “I affock “ASF Thom chem Wit o Newt prisy iw adfous fanaa alig SN Sbclion um pte rod on Ome hhemee Ts de de. aa gtd a—t> a oe H a ? an , a o a SY < GD lon” he — : f ao yor jm ~~ wo ~ = S y SNF Tp uate of sunsticn on leant obit, trom it ehouty 7 arredtllhat on SN2 Houalion phovs g oatal Mech y R-I > R-BH S Rea > RF : T” Jr lady Rooning qacoup amd c# bond in atrongort ond boner olifhioult 45 - cn a aaeee? Nuon = Se Ad b Hy CH, cH ch ,, CH= CH~ cf Ai . Roe ] Hel SO) OF Mat » Tad sell of founion of hitoymudiate fr indopndat of cone of wueQoophilie anol depundy only, on tone of sanctanbr. ae ea ) Tete oubetibahcn nuDeophibie wnimo) ; Yon py intend sede ak se a eamnanone cx _ Pasial Rect ston oxewr , Sy Rag ~ CHs-% —s eH® + xO > “Heth X —> chai® + x0 fH peak CH, — cH — ‘ i) x > 4 + x0 ~ a! a sree | ° Rake of saaéhioy 7 sso ao — oh, -c@ + 50 Or mort stable carbocation ia farmed, y Stable the frlormediate lomey the beat z Sagutra| De ee Ma CHs-CH=cH — el » CHa CHa CH el » Ha=CH— cH, 35251 SHe ney SNa & Si Sadho gy ea) Cou) Ts difforenbiak yuo Soe vont ne Comeept that the oH =e (5 CH= CH —cH, — oy + CH= CH—oH,— of —_ ots 1 th ( Hy CH, —O = cH , ee Howst it Joy squally fost om snp.