Important Organic II Reactions Flashcards

Printer Friendly

This set contains a plethora of important reactions covered in Organic Chemistry II as listed in chapters 15 - 24 of "Organic Chemistry" by David Klein.

Terms : Hide Images

1563208156	Preparation of Dienes from Allylic Halides Synthesis: 1) t-BuOK	0
1563208157	Preparation of Dienes from Dihalides Synthesis: 1) t-BuOK	1
1563208158	Diene Electrophilic Addition with HBr Synthesis: 1) HBr	2
1563208159	Diene Electrophilic Addition with Br2 Synthesis: 1) Br2	3
1563208160	Diels-Alder Reactions (1)	4
1563208161	Diels-Alder Retro Reactions (1)	5
1563208162	Diels-Alder Reactions (2)	6
1563208163	Diels-Alder Reactions (3)	7
1563208164	Diels-Alder Reactions (4)	8
1563208165	Diels-Alder Reactions (5)	9
1563208166	Electrocyclic Reactions (1)	10
1563208167	Electrocyclic Reactions (2)	11
1563208168	Electrocyclic Reactions (3) Synthesis: 1) Heat	12
1563208169	Electrocyclic Reactions (4) Synthesis: 1) hv	13
1563208170	Electrocyclic Reactions (5) Synthesis: 1) hv	14
1563208172	Electrocyclic Reactions (6) Synthesis: 1) Heat	15
1563208173	Sigmatropic Rearrangement (Cope) Synthesis: 1) Heat	16
1563208174	Sigmatropic Rearrangement (Claisen) Synthesis: 1) Heat	17
1563679689	Benzylic Position Oxidation Synthesis: 1) Na2Cr2O7, H2SO4, H2O 1) KMnO4, H2O, Heat 2) H3O+	18
1563679690	Benzylic Position Free-Radical Bromination Synthesis: 1) NBS, Heat	19
1563679691	Benzylic Position Elimination (E1) Synthesis: 1) Concentrated H2SO4	20
1563679692	Benzylic Position Elimination (E2) Synthesis: 1) NaOEt	21
1563679693	Benzylic Position Substitution (SN1) Synthesis: 1) H2O	22
1563679694	Benzylic Position Substitution (SN2) Synthesis: 1) NaOH	23
1563679695	Benzylic Catalytic Hydrogenation Synthesis: 1) Ni, 100 atm, 150° C	24
1563679696	Birch Reduction (1,2) Synthesis: 1) Na, CH3OH, NH3	25
1563679697	Birch Reduction (2,3) Synthesis: 1) Na, CH3OH, NH3	26
1563216499	Electrophilic Aromatic Substitutions (Br) Synthesis: 1) Br2, AlBR3	27
1563216500	Electrophilic Aromatic Substitutions (Cl) Synthesis: 1) Cl2, AlCl3	28
1563216501	Electrophilic Aromatic Substitutions (NO2) Synthesis: 1) HNO3, H2SO4	29
1563216502	Electrophilic Aromatic Substitutions (SO3H) Synthesis: 1) Fuming H2SO4	30
1563216503	Removing Electrophilic Aromatic Substitution (SO3H) Synthesis: 1) Dilute H2SO4	31
1563216504	Electrophilic Aromatic Substitutions (CH3) Synthesis: 1) CH3Cl, AlCl3	32
1563216505	Electrophilic Aromatic Substitutions (COCH2CH3) Synthesis: 1) ClCOCH2CH3, AlCl3	33
1563216506	Electrophilic Aromatic Substitutions (NH2) Synthesis: 1) Fe or Zn, HCl	34
1563216507	Electrophilic Aromatic Substitutions (CBr3) Synthesis: 1) Xs NBS	35
1563216508	Electrophilic Aromatic Substitutions (COOH) Synthesis: 1) KMnO4, NaOH, Heat 2) H3O+	36
1563216509	Electrophilic Aromatic Substitutions (CH2CH2CH3) Synthesis: 1) Zn(Hg), HCl, Heat	37
1563216510	Nucleophilic Aromatic Substitutions Synthesis: 1) NaOH, 70° C 2) H3O+	38
1563216511	Aromatic Elimination-Addition (OH) Synthesis: 1) NaOH, 350° C 2) H3O+	39
1563216512	Aromatic Elimination-Addition (NH2) Synthesis: 1) NaNH2, NH3 (l) 2) H3O+	40
1563220782	Hydrate Formation Synthesis: 1) [H+], H2O	41
1563220783	Acetal Formation Synthesis: 1) [H+], ROH, -H2O	42
1563220784	Cyclic Acetal Formation Synthesis: 1) [H+], HOCH2CH2OH, -H2O	43
1563220785	Cyclic Thioacetal Formation Synthesis: 1) [H+], HSCH2CH2SH, -H2O	44
1563220786	Imine Formation Synthesis: 1) [H+], RNH2, -H2O	45
1563220787	Enamine Formation Synthesis: 1) [H+], R2NH, -H2O	46
1563220788	Oxime Formation Synthesis: 1) [H+], NH2OH, -H2O	47
1563220789	Hydrazone Formation Synthesis: 1) [H+], NH2NH2, -H2O	48
1563220790	Reduction of a Ketone Synthesis: 1) LAH 2) H2O	49
1563220791	Grignard Reaction Synthesis: 1) RMgBr 2) H2O	50
1563220792	Cyanohydrin Formation Synthesis: 1) HCN, KCN	51
1563220793	Wittig Reaction Synthesis: 1) H2C=PPh3	52
1563220794	Baeyer-Villiger Oxidation Synthesis: 1) RCO3H	53
1563220795	Desulfurization Synthesis: 1) Raney Ni	54
1563220796	Wolf-Kishner Reduction Synthesis: 1) NaOH, H2O, Heat	55