— Most Organic Nowe Readion List {— © Finkelstein Reaction t- (formotion yf Allyl todides) RX +NoE — > R-I +NaXx X= ch, By @ Swarts Reaction 3- ( Bemottion a} abkyt fluoxide ) CH Br AGF —> CH3F + Ag Br ® ema Reaction + (formation of Aryl halide ) x Cs N or Sate Cr (Aryl habs) 7°? diazontum x=U, Br Galt ® Wurtz Reaction 2 CFemation 4 alkane) 2R-X +2Nq — 2 R-R 42Nax alkaw © Warde ~Fittig Reaction — (formelion of alkyLarene) x ether R Oo +Na +R-X Due cr +Nax abkyt-arerne Fitting Rendtion ¢ (rman gf doo aryl group are Joined jecthen ) Diy ether. ig Y Oe + 2Na = mee SO + 2NaX DiphenydKolbe!s Reactions. (Formation ¢ sabigghic acid) OH Na os Naol oe Coe cr Ors dy Ht (Sabrgyhic acid) Retmer- Tiemann Reaction? — (founeion J Sabicylaldelyd) IH OW Cyscrssns or" cy HF (Saligyoldlehyde) Williamson Synthesis >- (Rosmotion qd symmetateal and unsymmetrateal ether) RX + pi Na ——> p-o-f +Nax Friedel —Crafts Reackion 2 (Pormatin af Mkyl aed Acyd — benzen) Qi + cue on fs Cre rae) aad i Arhyole Cr? -c- sa oO + CHR i AL, Cacyd benzen) Rosermund. Reaction ° (Rorwation 4 Benzaldehyde ) ° vag He ae ce pd- B08, CHO (Benzaldehyde)® Stephen Reattion 2 — ( Forretion FI allehyd) 7 RecN +SnU,+HU ——> RCHENA BS gcro (aldehyde) @ Edad Reaction > (femation a} Benzatdelyd) CH ¢ cH (OC-OHY, CS 4 CxO, Uy, Co Ma or” _ bat, ( Benzaldehsde) Gattertman ~ Koch Readtion’- ( rmahion gf Bevzaldehyd,) 4 co, HW ure ‘@ Anhyd AlCls cute ee ) © Wolff ~ Kishner reduction Reaittion © (Formetion of alkane) chs, a cH. Neus NINH —e Kor /ethy-len ghyca oy » Ma DENN chy’ chy ph . chy ( Propane) Chemmencen reduction Reastion ?- (enrection g) akan) R . Noe oaths \n +HLO R ar@ Abdel Corderstion Reauto 2 (formation af fehydrny abdebyel andl Kefoves) ail Naoly OCH. CHO CHa pinche on . oa 2 CHU — eh, abn, eae OH @® Cannizzaro Reaction &- (Formetion of methanal , Beweyl allehal ) 4 ' \ eae Fae teen Kot Aa cto + exazemek w ¥ methanol 1H Coole Polassiums Fomade = 4 4 ton. NaoH —2 > ce = 4 7 Cowon a > Ae Berzye alcolal Sockium benzoate @ Kolbe ellechodysis Reachn & (Aanttion gf alkane) R-CooNa Seal ond ens R-H + Na, co, (alkane ) @ _ — Helk-Vobhard -Zekinsky Reaction? ( formation ef v—halo- ; Carboy de r gucn,cooy 2%. / Red P oe okt f Gi oaeaee R GH — Coot X (X= talacorbagybic x=,RBr aed JHoffmann Bromamialy deprodahion Reochion §- CRrmition gf prtinary ames J o Re tS Ni Bq HA Nosh ——> Q-NH, +Na, Co +2NoBy 42H, 0 (amuive )