Recall from chapter 6 that, in many ways, the proton transfer process in a Brønsted-Lowry acid-base reaction can be thought of as simply a special kind of nucleophilic substitution reaction, one in which the electrophile is a hydrogen rather than a carbon.
In both reaction types, we are looking at very similar players: an electron-rich species (the nucleophile/base) attacks an electron-poor species (the electrophile/proton), driving off the leaving group/conjugate base.
In the next few sections, we are going to be discussing some general aspects of nucleophilic substitution reactions, and in doing so it will simplify things greatly if we can use some abbreviations and generalizations before we dive into real examples.
Instead of showing a specific nucleophile like hydroxide, we will simply refer to the nucleophilic reactant as ‘Nu’. In a similar fashion, we will call the leaving group ‘X’. We will see as we study actual reactions that leaving groups are sometimes negatively charged, sometimes neutral, and sometimes positively charged. We will also see some examples of nucleophiles that are negatively charged and some that are neutral. Therefore, in this general picture we will not include a charge designation on the ‘X’ or ‘Nu’ species. In the same way, we will see later that nucleophiles and leaving groups are sometimes protonated and sometimes not, so for now, for the sake of simplicity, we will not include protons on ‘Nu’ or ‘X’. We will generalize the three other groups bonded on the electrophilic central carbon as R1, R2, and R3: these symbols could represent hydrogens as well as alkyl groups. Finally, in order to keep figures from becoming too crowded, we will use in most cases the line structure convention in which the central, electrophilic carbon is not drawn out as a ‘C’.
Here, then, is the generalized picture of a concerted (single-step) nucleophilic substitution reaction. Note that this representation does not include the charges that would be present on Nu and X.
- 8.1: Introduction to the nucleophilic substitution reaction. Authored by: Tim Soderbergu00a0(University of Minnesota, Morris). Located at: https://chem.libretexts.org/Textbook_Maps/Organic_Chemistry/Book%3A_Organic_Chemistry_with_a_Biological_Emphasis_(Soderberg)/Chapter_08%3A_Nucleophilic_substitution_reactions_I/8.1%3A_Introduction_to_the_nucleophilic_substitution_reaction. License: CC BY-NC-SA: Attribution-NonCommercial-ShareAlike