Interactions | Reactions | Processes
Classified as: Substitution: Concerted
Second order nucleophilic and radical substitution reactions are concerted.
For more information look in the Chemogenesis webbook section substitution, transfer, abstraction, displacement (STAD).RCOOH |
+ |
CH2N2 |
+ |
N2 |
+ |
[N3]– |
+ |
Cl– |
+ |
CH3COOH |
+ |
+ |
HCl |
CH3I |
+ |
[OH]– |
CH3OH |
+ |
I– |
CH3I |
+ |
(CH3)3N |
[(CH3)4N]+ |
+ |
I– |
[(CH3)4N]+ |
+ |
[OH]– |
CH3OH |
+ |
(CH3)3N |
[(CH3)4N]+ |
+ |
H2S |
[CH3–SH2]+ |
+ |
(CH3)3N |
(CH3)2CHBr |
+ |
CH3CH2O– |
+ |
CH3CH2OH |
CH3–CH=CH2 |
+ |
+ |
Br– |
+ |
CH3CH2OH |
+ |
[OH]– |
+ |
(CH3)3N |
CH2ClCH2Cl |
+ |
2 |
PhS(CH2)2SPh |
+ |
2 |
Cl– |
(CH3)2CHBr |
+ |
+ |
Br– |
+ |
CH3I |
+ |
I– |
+ |
Br2 |
+ |
[Et3O]+[BF4]– |
+ |
+ |
+ |
Li+ |
+ |
[BF4]– |
+ |
+ |
CH3CH2I |
+ |
+ |
Li+ |
+ |
I– |
CH3I |
+ |
[SCN]– |
N≡C–S–CH3 |
RCOCl |
+ |
[SCN]– |
CH3I |
+ |
[NO2]– |
CH3–NO2 |
CH3I |
+ |
+ |
R–I |
+ |
NaCN |
R–CN |
+ |
NaI |
R2NH |
+ |
HNO2 |
R2N–NO |
[R–S]– |
+ |
N≡C–Cl |
R–S–C≡N |
+ |
Cl– |
RMgX |
+ |
N≡C–Cl |
R–CN |
+ |
Cl– |
RMgX |
+ |
I–C≡N |
R–I |
+ |
[CN]– |
ZrC |
+ |
3 |
Pt |
ZrPt3 |
+ |
C |
+ |
AlCl3 |
+ |
[AlCl4]– |
+ |
AlCl3 |
+ |
[AlCl4]– |
© Mark R. Leach 1999 –
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