This is important throughout organic chemistry, but will be especially important when trying to determine the products of elimination

and substitution (E1, E2, SN1, SN2)reactions. There are generally three trends to remember when discussing how nucleophilic a
reactant is:
1) Size - Generally, the more linear and/or smaller the nucleophile, the more nucleophilic it will be. This is because it can
react at more sites and will not be sterically hindered if it is smaller or linear.
2) Electronegativity- The more electronegative an atom is, the less nucleophilic it will be. This is because more
electronegative atoms will hold electron density closer, and therefore will be less likely to let that electron density
participate in a reaction. We see this in calculations and experiments that show nucleophilicity decreases as you get closer
to fluorine on the periodic table (C > N > O > F)
3) Polarizability- The more polarizable an atom is, the more nucleophilic it will be. Polarizability is defined as the ability to
distort the electron cloud of an atom, which allows it interact with a reaction site more easily. Generally, polarizability
increases as you travel down a column of the periodic table (I > Br > Cl > F)
Below is a table of relative nucleophilic strength. This is relative because nucleophilic strength is also dependant on other factors in
the reaction, such as solvent.

VERY
Good
HS-, I-, RSnucleoph
iles
Good
nucleoph Br-, HO-, RO-, CN-, N3iles
Fair
nucleoph
NH3, Cl-, F-, RCO2iles
Weak
nucleoph
H2O, ROH
iles
VERY
weak
RCO2H
nucleoph
iles
As shown above, as a general rule, the anion of a reactant will be a better nucleophile than the neutral form. (i.e. RCO2- is a better
nucleophile than RCO2H)