"This is SN2"

This is SN2
Substitution Nucleophilic bimolecular
This is SN2
Backside attack from the 'N' so show it some love.
This is SN2
Substitution Nucleophilic bimolecular
This is SN2
Backside attack from the 'N' so show it some love.
(Sam aka C-Unit)
Second order, uhh, rate constant, uhh
Depends on both, reactants, uhh.
You don't want none,
Halide better run.
When attack is on N inverts those, bonds.
Carbon gets some,
Nucleophile fun
Planar transition as the halide, runs.
N will, bond
Ready here it comes,
Carbons, uhh,
Only tetrahedral ones.
Less sub'd carbon, for the best reaction.
First sub'd cheers while the third says �uhhhh�
N gives a swift punt,
These nucleophiles just wanna have fun
With electrons
On its oxy-gen
Attacking carbon with lone pairs like, uhh
Substitution son, halide leaves and its done
Reaction diagram is a one hump stunt.
(Jenn aka Halide Havok)
I put N's on carbon that's how I do
Halides so scared they make a good leaving group
One transition man, carbons so changed
I have an five bond carbon on it's transition state (Ah!)
N will, bond me, halide, leave me,
Final product just how we like it, girl
Carbon start with four bonds so it end with four bonds,
Sigma bonds are the best!
They say N's so good
Always understood
To attack carbon of the compound
It if attacks proton, and forms an alkene
Somebody must be using it as base
At low Celsius, N has a blast
N attacks carbon, halides now the past
For an instant, overfilled e- stash
Timid ol' halide, why you always dash

This is SN2
Substitution nucleophilic bimolecular
This is SN2
Backside attack from the 'N' so show it some love.
This is SN2
Substitution nucleophilic bimolecular
This is SN2
Backside attack from the 'N' so show it some love.