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Functional group nomenclature in organic compounds

Learn about the nomenclature rules for functional groups in organic compounds. Understand how to name alkanes, alkenes, alcohols, and more.

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Functional group nomenclature in organic compounds

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  1. izLrqrdÙkkZ %&MkW ;ksxsUnz dqekj dksBkjhO;k[;krk&jlk;u'kkldh; mR—"V mPprj ek/;fed fo|ky;ek/kouxj & mTtSu

  2. fØ;kRed lewg,oaIUPAC ukedj.k ds fu;e

  3. bl v/;k; dk v/;;u djus ds i’pkr~ fo|kFkhZ %&1- fØ;kRed lewg dks ifj“kf"kr dj ldsxsaA2- dkcZfud ;kSfxdks esa fØ;kRed lewg dh igpku Kkr dj ldsxsaA3- dkcZfud ;kSfxdks ds IUPAC ukedj.k ds fu;e tku ldsxsaA4- dkcZfud ;kSfxdks ds lw= ns[kdj IUPAC uke fy[k ldsxsA5- IUPAC uke ds vk/kkj ij ;kSfxdks dk lw= fy[k ldsxsa

  4. fØ;kRed lewgifjHkk"kk %& dkcZfud ;kSfxd esa v.kq dk og Hkkx tks ;kSfxd ds jklk;fud xq.kkssa dks fu/kkZfjr djrk gS] fØ;kRed lewg (Functional group) dgykrk gSAtSls %& C2H5OH ,fFky ,YdksgkWy es &OH fØ;kRed lewg gSA

  5. lkj.kh Ø- dkcZfud ;kSfxd dk uke lw= lw= fØ;kRed lewg 8 ,flVkby DyksjkbM CH3COCl – COCl &,flM gSykbM 9 ,flVkekbM CH3CONH2 – CONH2 &,ekbM 10 ,lhfVd ,ugkbMªªªkbM CH3– CO CH3– CO – CO – CO &,ugkbMªkbM >O >O 11 ,fFky ,ehu C2H5NH2 – NH2 &,ehuks 12 ukbVªks esFksu C2H5NO2 – NO2 &ukbVªks 13 essfFky lk;ukbM CH3CN – CN &lk;ukbM 14 esfFky vkblks lk;ukbM CH3NC – NC &vkblkslk;ukbM fØ;kRed lewg ds ckn 'ks"k cps lewg dks ,fYdy lewg dgrs gSaA

  6. IUPAC ukedj.k iz.kkyh & lu~ 1982 esa ftusok esa vUrjk"Vªh; dkUQzsal esa dkcZfud ;kSfxdksa ds ukedj.k ds fy;s ,d iz.kkyh fodflr gqbZ ftls International Union Of Pure and Applied Chemistry dgrs gS] laf{kIr esa ;g IUPAC iz.kkyh dgykrh gSA1- ,Ydsu dk ukedj.k ;s lar`Ir gkbMksdkcZu gksrs gS budk lkekU; lw= CnH2n+2 gksrk gS IUPAC i)fr ds vuqlkj buds uke ds vUr esa ,su (ane) yxkrs gSA fu;e bl izdkj gS%& A yEch dkcZu J`a[kyk dk p;u djuk & dkcZfud ;kSfxdks ,Ydsu esa yach dkcZu J`a[kyk dk p;u djds dkcZu ijek.kq dks la[;k ds vuq:i eq[; bdkbZ dk ukedj.k djds vUr esa vuq:Ik ane yxknsrs gSA

  7. CH3 - CH-CH2-CH2-CH2-CH3 CH2 CH3 dkcZu J`a[kyk iwoZyXu vuqyXuC1 esFk ,suC2 ,sFk ,suC3 izksi ,suC4 C;wV ,su C5 isaV ,su C6 gsDl ,sumnkgj.k %& bl lw= esa yEch J~a[kyk 7 dkcZu ijek.kqvksa dh gSA

  8. B yEch J`a[kyk esa dkcZu ijek.kqvksas dk vdau & dkcZu J`a[kyk esa dkcZu ijek.kqvksa dk vdau ml vksj ls djrs gS ftl vkSj ls izfrLFkkih lewg fudV gksrk gSA mnkgj.k .CH3 CH3 - CH- CH2 - CH2 - CH3 12 3 4 5 .CH3 CH3 - CH- CH2 - CH2 - CH3 54 3 2 1 ¼ 2& esfFky isUVsu ½ lgh uke ¼ 4& esfFky isUVsu ½ xyr uke

  9. Cvdksa dk ;ksx U;wure gks&dkcZu J`a[kyk esa ;fn ,d ls vf/kd izfrLFkk;h lewg gks rks vadu ml vksj ls djrs gS ft/kj ls vadks dk ;ksx U;wure gksaA .CH3 CH3 CH3 - C- CH2 - CH2 – C- CH3 5 4 3 2 1 6 CH2 CH3 7 CH3 .CH3 CH3 CH3 - C- CH2 - CH2 – C- CH3 3 4 5 6 7 2 CH2 CH3 1 CH3 izfrLFkk;h lewg dk ;ksx 2 $ 2 $ 5 $ 5 ¾ 14 3 $ 3 $ 6 $ 6 ¾ 18 lgh uke xyr uke 2]2]5]5& VsVªkesfFky gsIVsu 3]3]6]6& VsVªkesfFky gsIVsu

  10. D izfrLFkk;h lewgksa dks vaxzsth o.kZekyk ds Øe esa fy[kuk &;fn dkcZu J`a[kyk esa ,d ls vf/kd izfrLFkk;h lewg gks rks mUgs vaxzsth o.kZekyk ds Øe esa fy[krs gSA mnkgj.k 1 2 3 4 5 CH3& CH & CH & CH & CH3 CH3 CH2 CH3 CH3 3& ,fFky 2]4]& Mk; esfFky isUVsu

  11. vH;kl iz’u 1- fuEu ;kSfxdks dk IUPAC uke fyf[k;s CH3 CH3- C- CH3 CH3 Answer :- CH3- C- CH3 esa dkcZu J`a[kyk 3 ijek.kqvksa dh gSA dkcZu 2 ij 2 CH3 lewg gSa] CH3 CH3- C- CH3 CH3 vr% lgh uke 2]2 & MkbZ esfFky izzksisu gSA 1 2 3

  12. 1 2 3 4 1 2 3 4 ,Ydhu ,oa ,Ydkbu dk ukedj.k &,Ydhu ,oa ,Ydkbu valr`Ir gkbMksdkcZu gS] ,Ydhu dk lkekU; lw= CnH2n ,oa ,Ydkbu dk lkekU; lw= CnH2n-2 gksrk gSA,Ydhu ds ukedj.k ds fy;s laxr ,Ydsu ds uke ds vUr esa –ane gVkdj –ene yxkrs gSA mnkgj.k CH3CH = CH- CH3 2&C;wVhu ¼ C;wV + bZu ½,Ydkbu ds ukedj.k ds fy;s laxr ,Ydsu ds uke ds vUr esa –ane gVkdj –ene yxkrs gSAmnkgj.kCH3-C= C-CH32&C;wVhu ¼ C;wV + vkbu ½

  13. vH;kl iz’u 1- fuEu ;ksfxd dk IUPAC uke fyf[k;s CH = C- CH- CH2 - CH3 Answer :- bl ;kSfxd dk lgh uke 1& isUVkbu gSA 1 2 3 4 5

  14. 3 ,fYdy gSykbM dk ukedj.k &,fYdy gSykbM ds ukedj.k ds fy;s ,Ydsu ds vkxs gsykstu ewyd dk fy[krs gSaA tSls&CH3CH2CH2Clblesa 3 dkcZu dh J`a[kyk gS vr% ewy ,Ydsu izksisu gqvk vr% bldk IUPAC uke 1- Dyksjks izksisu gksxkA 3 2 1

  15. ANSWER CH2-CH2-CH2-CH2 Cl Br 1&czkseks] 3& Dyksjks C;wVsu 4 3 2 1 vH;kl iz’u CH2-CH2-CH2-CH2 Cl Brdk IUPAC uke D;k gSA

  16. 4- Mkbgsykstu O;qRiUu dk ukedj.k& tSls & ,fFkyhu czksekbM CH2BrCH2Br 1]2 Mkbczkseks ,Fksu5- Vªkb gSykstu O;qRiUu dk ukedj.k & tSls & DyksjksQkeZCHCl3 1]1]1 Vªk; Dyksjks esFksu 1 2

  17. 6- eksuks gkbgfMªd ,sYdksgy dk ukedj.k&,Ydksgy ds IUPAC ukedj.k esa laxr ,Ydsu ds uke ds vUr esa e dks gVkdj vkWy (ol) yxk nsrs gSaA tSls & Alkane + Ol = Alkanol ,fFky ,Ydksgy & CH3CH2OH & ,Fksuky C;wfVy ,Ydksgy & CH3CH2CH2OH & C;wVsu&1&vky7- Mkb gkbfMªd ,sYdksgy dk ukedj.k &IUPAC ukedj.k ds le; ,Ydsu esa vuqyXu Mkbvky (diol) tksM+rs gSaA lk/kkj.k uke IUPAC ukeCH2OH Xyk;dky ,Fksu 1]2 MkbvkWyCH2OH 1 2

  18. 8- Vªkb gkbgfMªd ,sYdksgy dk ukedj.k&IUPAC ukedj.k ds le; ,Ydsu esa vuqyXu Vªkbvky (Triol) tksM+rs gSaA lk/kkj.k uke IUPAC ukeCH2OH fXyljky izksisuu 1]2]3 VªkbvkWyCHOH CH2OH 1 2 3

  19. 9- bZFkj dk ukedj.k &IUPAC i)fr ds vuqlkj bZFkj dks ,Ydsu dk ,YdkWDlh O;qRiUu ekurs gSaSR- O – R ,YdkWDlh ,Ydsulk/kkj.k uke IUPAC ukeCH3 – O – CH3 Mkb esfFky bZFkj esFkkWDlh esFksuCH3 – O – C2H5 ,fFky esfFky bZFkj esFkkWDlh ,Fksu

  20. 10- eksuks dkcksZfDlfyd vEy dk ukedj.k&IUPAC i)fr ds vuqlkj ,Ydsu ds uke ds vUr esa e gVkdj vksbd vEy(Oic Acid) yxk nsrs gSaA tSls lk/kkj.k uke IUPAC ukeHCOOH QkWsfed vEy esFksuksbd vEyCH3COOH ,lhfVd vEy ,sFksuksbd vEy

  21. 11- ,YMhgkbM dk ukedj.k &IUPAC i)fr ds vuqlkj laxr ,Ydsu ds e dks gVkdj al ¼vy½ yxk nsrs gSaSaA Alkane + al = AlkanaltSls lk/kkj.k uke IUPAC ukeHCHO QkWsesZYMhgkbM vEy esFksuyCH3CHO ,lhVsYMhgkbM ,sFksuy

  22. 12- dhVksu dk ukedj.k&IUPAC i)fr ds vuqlkj laxr ,Ydsu ds e dks gVkdj one ¼vksu½ yxk nsrs gSaSaAAlkane + one = AlkanonetSls lk/kkj.k uke IUPAC ukeCH3COCH3 ,lhVksu 2& izksisuksuCH3COCH2CH3 ,fFky esfFky dhVksu 2& C;wVsuksu1

  23. 13- ,YMhgkbM dk ukedj.k &IUPAC i)fr ds vuqlkj vEy DyksjkbM ds ukedj.k ds fy;s laxr vEy esa ic Acid ds LFkku ij yl Choride yxk nsrs gSaSaA Alkanoic Acid + yl ChloridetSls lk/kkj.k uke IUPAC ukeCH3COCl ,lhVkby DyksjkbM ,Fksuksby DyksjkbM

  24. 14- ,flM ,ugkbMªkbM dk ukedj.k&IUPAC i)fr ds vuqlkj laxr vEy ds IUPAC uke esa ls vEy 'kCn ds LFkku ij ,ugkbMªkbM yxk nsrs gSaSaAAlkanoic Acid + Anhydride = Alkanoic AnhydridetSls lk/kkj.k uke IUPAC ukeCH3CO CO ,lhfVd ,ugkMªkbM ,Fksuksbd ,ugkbMªkbMCH3CO

  25. 15- ,flM ,ekbM dk ukedj.k &IUPAC i)fr ds vuqlkj laxr vEy ds IUPAC uke es ls oic Acid ds LFkku ij ,ekbM yxk nsrs gSaSaAAlkanoic Acid + Amide = Alkanamide tSls lk/kkj.k uke IUPAC ukeCH3CONH2 ,slsVsekbV ,FksusekbMCH3CH2CONH2izksfivku ,sekbM izksisuSekbM

  26. 16- ,LVj dk ukedj.k&blesa ,d ,fYdy lewg rFkk 'ks“k bdkbZ laxr vEy ds vuqyXu ls bd gVkdj ,V (ate) yxk nsrs gSaA Alkyl Alkanoic Acid + ate tSls lk/kkj.k uke IUPAC ukeCH3COOCH3 esfFky ,slhVsV esfFky esFksuks,VCH3COOC2H5,fFky ,slhVsV ,sfFky ,sFksuks,V

  27. 17- ,flM dk ukedj.k &IUPAC ukedj.k ds fy, ,ehuks 'kCn ,Ydsu ds vkxs yxk nsrs gSaSaA tSls lk/kkj.k uke IUPAC ukeCH3NH2 esfFky ,ehu ,ehuks esFksuC2H5NH2,fFky ,ehu ,ehuks ,sFksu

  28. 18- ukbVªks ;kSfxd dk ukedj.k&IUPAC ukedj.k ds fy, ukbVªks ,Ydsu iz;qä djrs gSaAC2H5NO2ukbVªks ,sFksu

  29. vH;kl iz’ufuEu ;kSfxdks ds lw= fyf[k;s &¼1½ 1]3 C;wVkMkbu ¼2½ 2& Dyksjks izksisu ¼3½ isUV &1& bZu&4&vkbu ¼4½ esFksuksbd vEy ¼5½ ,FksuyAnswer1. CH2=CH-CH=CH22. CH2-CH-CH2 Cl3. CH=C-CH2-CH=CH24. HCOOH5. CH3CH2OH

  30. vH;kl iz’ufuEu ;kSfxdks ds lw= fyf[k;s &¼1½ ,FkkWDlh ,Fksu ¼2½ 2& ,ehukss izksisu ¼3½ 2&ukbVªks C;wVsu ¼4½ izksisuekbM¼5½ 2&izksisuksuAnswer1. C2H5 - O – C2H5 5. CH3COCH3 2. CH3-CH-CH3 NH23. CH3 - CH – CH2 – CH3 NO24. CH3CH3CONH2

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