Izomeria compusilor organici

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ReacŃii ce includ compuşi optic activi • reacŃii ce au loc la atomul de carbon chiral • reacŃii ce nu au loc la atomul de carbon chiral • reacŃii ce generează un nou atom de carbon chiral
ReacŃii ce au loc la atomul de carbon chiral Inversia configuraŃiei(SN2) H O H 3C H C 2H 5 O O S O (R)-2-butil tosilat C2H5 Racemizarea Racemizarea(SN1) H3C CH(CH 3) 2 C RetenŃia configuraŃiei Br (R) CH 3 H3CH 2C O H C OH+Cl S Cl -HCl H3C C 2H 5 Cl H3CH 2C S H H 3C C O HO CH 3 H C 2H 5 + (S)-(+)-2-butanol a H 3C C O lent Br - O CH(CH 3) 2 O S O CH 3CH 2OH CH3CH 2OH b CH 2CH Cl 3 H C + S O H3C b a CH 3 OCH 2CH 3 C2H C 5 CH(CH H 3) 2 3C (S) (inversie) C2H5 H3C CH(CH 3) 2 C Br (R) (retentie) H3CH 2C rapid O H C Cl -SO2 H3C
Page 1 and 2: Izomeria zomeria compusilor organic
Page 3 and 4: Stereoizomeria Izomeria de conforma
Page 5 and 6: ConformaŃiile butanului H H 3C ϕ=
Page 7 and 8: Izomeria de configuraŃie Izomeria
Page 9 and 10: Nomenclatura E-Z pentru izomerii ge
Page 11 and 12: Izomeria geometrică a H CH 3 H cic
Page 13 and 14: Activitatea optică Activitatea op
Page 15 and 16: Chiralitatea chiralitatea- proprie
Page 17 and 18: C 2 H A H B C2 HB HA H CH3 H3C H H3
Page 19 and 20: H C * COOH CH 3 OH acid lactic b a
Page 21 and 22: H Formulele de reprezentare a enant
Page 23 and 24: ConfiguraŃia relativă după conve
Page 25 and 26: Conventia RS in cazul formulelor Fi
Page 27 and 28: Izomeria optică la compuşii cu do
Page 29 and 30: I III II IV CHO CHO CHO CHO H OH H
Page 31 and 32: AMESTEC RACEMIC, FORMA MEZO Racemi
Page 33: Prochiralitate protoni H CH3 H dias
Page 37 and 38: ReacŃii ce generează un nou centr
Page 39 and 40: HO (S)-2-butanol (R)-2-butanol Rezo
Page 41 and 42: CLASIFICAREA COMPUŞILOR ORGANICI

Izomeria compusilor organici

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