
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 |
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CH2N2 |
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N2 |
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+ |
[N3]– |
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Cl– |
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CH3COOH |
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+ |
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HCl |
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CH3I |
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[OH]– |
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CH3OH |
+ |
I– |
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CH3I |
+ |
(CH3)3N |
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[(CH3)4N]+ |
+ |
I– |
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[(CH3)4N]+ |
+ |
[OH]– |
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CH3OH |
+ |
(CH3)3N |
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[(CH3)4N]+ |
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H2S |
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[CH3–SH2]+ |
+ |
(CH3)3N |
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(CH3)2CHBr |
+ |
CH3CH2O– |
+ |
CH3CH2OH |
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CH3–CH=CH2 |
+ |
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+ |
Br– |
+ |
CH3CH2OH |
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+ |
[OH]– |
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+ |
(CH3)3N |
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CH2ClCH2Cl |
+ |
2 |
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PhS(CH2)2SPh |
+ |
2 |
Cl– |
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(CH3)2CHBr |
+ |
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+ |
Br– |
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CH3I |
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I– |
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+ |
Br2 |
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+ |
[Et3O]+[BF4]– |
+ |
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+ |
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+ |
Li+ |
+ |
[BF4]– |
+ |
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+ |
CH3CH2I |
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Li+ |
+ |
I– |
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CH3I |
+ |
[SCN]– |
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N≡C–S–CH3 |
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RCOCl |
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[SCN]– |
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CH3I |
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[NO2]– |
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CH3–NO2 |
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CH3I |
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R–I |
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NaCN |
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R–CN |
+ |
NaI |
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R2NH |
+ |
HNO2 |
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R2N–NO |
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[R–S]– |
+ |
N≡C–Cl |
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R–S–C≡N |
+ |
Cl– |
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RMgX |
+ |
N≡C–Cl |
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R–CN |
+ |
Cl– |
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RMgX |
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I–C≡N |
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R–I |
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[CN]– |
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ZrC |
+ |
3 |
Pt |
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ZrPt3 |
+ |
C |
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AlCl3 |
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[AlCl4]– |
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AlCl3 |
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[AlCl4]– |
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© Mark R. Leach 1999 –
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