IUPAC NOMENCLATURE OF ORGANIC Compounns (BD) (UPAC NOmENcLATURE OF ALKANE 4. Rule fav main cham selection :-(rod] c> oe Seh > Lowert Pasitinsile abpieh. sub) @ Select Angent cantor Carb chain 0d parsnk chain © When more then one Aagot chains ara prerent in comPpond, then select ‘ax. 0+ 4 substitvend Contanivg chem a> Pansat chain. © When no- 4 substituents ara ods Asme them fowext get 4 postin Of sw. contsuring chain will be rain Chain @ when ook of" fosihon of sub ov. ode Bame then conider alfprabekica, ord, of vam >} substifent «IUPAC NOMENCLATURE OF ORGANIC Compounns (BD) (UPAC NOmENcLATURE OF ALKANE % Rute for nobowng gf movin chen ® Give the number 4 ain from tek corner whidh har Lowest sth 46 position +t Sulos hos ® When st + positim -f Gr eed a ee sia dat Corners Jhon conser ootbebebiad 1dr fr morboang GB) @ wowle the rame ef substners alphabchok order with fosrhon © whem rare thn me AAme simple, Sub: 2x FOE thom ude dtr, tera, Ponds ck efor of swosIUPAC NOMENCLATURE OF ORGANIC Compounns, (BD) (UPAC NOmENcLATURE OF ALKANE © When more ten one Same complex Substbeks are prow thon wt (Bis For tee same compl suehinnad Tes = + Tore" Tehokis= > fe ' 6 _ on Rewde skis = S -- - ——- rakis= 9G -_ «=. ch befve name CI Camylex Sue @ @ Follsamg ovr consider in alftabehcal orden iso, New, [db,tei, febre ede} comple Sub- ann vat Cansioer in Wlphabehical srs @ sec, fat, (aii, tebe dy simple 88) bis, Hrs, fefrsks —IUPAC NOMENCLATURE (@) IUPAC NomencuaTvRe OF ALKANE ; Zhebye Phe wed net 1Stte Ep) re AA - Rewtane 2 sA 7 3 Metyphexan, NN tykhexane zi awv &» SR PRB fae Pomeothetong _ | P Pipe reg 4. vas = 288. Kemet facts AY = 2au Taino pontine % Ra, yy Rwy OF onnnme Compounns,IUPAC NOMENCLATURE OF ORGANIC comPounDs (@) [IUPAC NomencuaATURE OF ALKANE : amebyten( | dooney oan e (iméonecd = 4-(1 Dinah) _s-medifoctane (cowect) pte 24442 Poakomelep 3rbis( sme one = “one 3.0i vera BUY dec? MonaneIUPAC NOMENCLATURE OF ORGANIC Compounds a ow OAL, = 280m vchbropectene ¥ ov a _ 4 Bers p- LOAI60 Poutane ON = _— eee ~ bi _|-Chlavs peudane g wa by \ oA =Ht59 > 4 Bromg 2,2-didn pine ® Me Sees 5 5 Fes - 2 duchlor hexane PR2IDK © 3 Age > 2 Brom u-chlany 3+ charsIUPAC NOMENCLATURE OF ORGANIC Compounds ae Oe = t.Bromo92-dichlan 5: eayfpocce “os by ® LO" gt Dibroony.1- Chore. 5Cyl portare 22Di boone -3 (enliovetyheptane 2chlen’ A 5.( ye Dibr.29. ccs UrlecaeIUPAC NOMENCLATURE OF ORGANIC Compounds = 2broras 5. Chlen 4-(dsbrome mel -3- (trictleromelil) horane a Apion , yr Taher -2- reyf. set ne, Ahem %IUPAC NOMENCLATURE OF ORGANIC Compounds Common rome off Alkane ond obkyt subshivouts AlKanes alkene) n-Ailkone Ge . oe one motyt ov TS position of Sept darn “Neo alkene | 1s0 butane Tob rnd pet on tisten Ay wbstone 4 suagif ain AA 1 Posters Dv \sobedane >K New penne _ hexane 7 w crane Ld IT 450! oe hexane wtf Cie Nae = 150 and *09 applicable Uph six coakin ooIUPAC NOMENCLATURE OF ORGANIC Compounds Common rome off Alkane ond obkyt subshivouts Trey ~ AM ‘Iso octane yp wl fol > Odene no. sale Trobubome Tsvbukene Tsooctene + Octane NO = 100 -Heptine octene no =O > Sample J pels! > octsne no=70f Lehrer 7 Brchivg Teaoctone nolyCommon Tame of Alkower avd alkyl Subshivots fee Allgk Subshtents— © Wie nc-orag— m-pref (-¢-¢-c— n= bly (Cece = ni Pobyh Cate CHEER Memon © sec ahhh: —c See. Pap _ oe pop Cisef tg c-c-<-< See babgp |IUPAC NOMENCLATURE OF ORGANIC Compounds Common rome off Alkane ond obkyt subshious © Tet — cde Tod. butyf oe. Tent. Pewdef @ bselife iso preyp See Teb 7 “dt coc Tso porlyp < Cc Tse hex oo ?