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Substitution Reactions

By James Ashenhurst

The SN2 Mechanism

Last updated: March 22nd, 2019

Having gone through the two different types of substitution reactions, and talked about nucleophiles and electrophiles, we’re finally in a position to reveal the mechanism for one of the most important reactions in organic chemistry.

It’s called the SN2 reaction, and it’s going to be super useful for us going forward.

Let’s look at the data first.

1. The Reaction Proceeds With Inversion of Configuration

When we start with a molecule with a chiral center, such as (S)-2-bromobutane, this class of reaction results in inversion of stereochemistry. Note how we start with (S)-2-bromobutane and end up with (R)-2-methylbutanenitrile. 

2. The Rate Law Is Second Order Overall

Note how the rate of the reaction is dependent on both the concentration of the nucleophile and that of the substrate. In other words, it’s a second-order reaction.

3. The Reaction Rate Is Fastest For Small Alkyl Halides

Finally, note how changes in the substitution pattern of the alkyl halide results in dramatic changes in the rate of the reaction.* “Smaller” alkyl halides like methyl bromide are fast, while more highly substituted tertiary alkyl bromide doesn’t proceed at all.

Taking all this data into consideration, we refer to this reaction as the SN2 mechanism. What does SN2 stand for?

  • Substitution
  • Nucleophilic
  • molecules in the rate determining step

So how does it work?

The SN2 Mechanism Proceeds Through A Concerted Backside Attack Of The Nucleophile Upon The Alkyl Halide

The best explanation we have for what happens in this reaction is that it proceeds through what organic chemists refer to as a backside attack.  The nucleophile approaches the alkyl halide 180° from the C-Br bond, and as the C-(nucleophile) bond forms, the C-(leaving group) bond breaks.** At the transition state of the reaction, there are partial C-(nucleophile) and C-(leaving group) bonds (denoted by dashed lines). Note the geometry too – instead of tetrahedral, it’s trigonal bipyramidal. This is 5-coordinate carbon – if only for a femtosecond or two.

And in an analogy you’ll no doubt hear many times, then,  like an umbrella in a strong wind, the three groups flip over as the leaving group leaves, resulting in inversion of configuration. Note that inversion happens at carbons without stereocenters too – it’s just that we can’t observe it because there’s no way to detect the change in configuration.

This umbrella metaphor for the backside attack mechanism is so fundamental and well known in organic chemistry that you can tweet about it and people will know exactly what you mean.

In the next post, we’ll show some more examples of this reaction and explain why it’s one of the most useful reactions in chemistry.

P.S. You may remember that Freda also took this awesome picture of an ozonolysis reaction.

Next Post: Why The SN2 Is Powerful

*Numbers are approximate. Source – Smith, M. and March, J. L. “March’s Advanced Organic Chemistry” 5th ed.

** backside attack, because the nucleophile donates a pair of electrons into the most accessible empty orbital, which is the antibonding (σ*) orbital of the C-(leaving group) bond, which resides at 180° to the bond. Donation of a pair of electrons into the antibonding orbital results in cleavage of the bond. It’s kind of like an “eject button” in that way.

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Comment section

11 thoughts on “The SN2 Mechanism

  1. Primary halides which have an unsaturated group attached to the carbon react
    much faster than bromomethane in SN2 reactions.

  2. Thank u so much for your website you make everything so easy to understand and this website is literally saving my life rn for my exam

  3. Hi James,

    Great post. Just want to clarify, would there be any positive charge on the carbon in the transition state as shown in the mechanism ?


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