The
SN1 reaction is an
organic reaction in
chemistry. "S
N" stands for
substitution nucleophilic and the "1" represents the fact that the
rate-determining step[?] take place on the first order, that is it happens with only one
molecule. Increasing or decreasing the
concentration of that kind of molecule in a
closed system[?] changes the rate of the reaction in a
direct relationship[?].
The SN1 reaction takes place in two steps:
- Changing the carbon centre:
- Formation of a carbocation: due to the separates of leaving group (molecule A) from the carbon.
- Nucleophilic attack[?]: a nucleophile (molecule B) joins onto the carbon.
- Deprotonation: Removal of a proton on the protonated nucleophile by a molecule (sometimes the same species as A) in the solvent, usually protic.
An example reaction:
- C(CH3)3Br --> C(CH3)3+ + Br-
- C(CH3)3+ + OH- --> C(CH3)3OH
This gives the overall reaction:
- C(CH3)3Br + OH- --> C(CH3)3OH + Br-
SN1 occurs where the central carbon atom is surrounded by bulky groups. The rate depends only on the concentration of the substrate.
- rate = k[RX]
Nucleophilicity is irrelevant in the determining step's rate, in which only the substrate is crucial.
Because the intermediate cation, R+, is planar, an optically active[?] substrate gives a racemic mixture because nucleophilic attack[?] can occur from either side.
- Diagrams (http://www.chemhelper.com/sn1.html): Frostburg State University
- Excercise (http://www.usm.maine.edu/~newton/Chy251_253/Lectures/Sn1/Sn1FS.html): the University of Maine