Login-Verarbeitung ...

Trial ends in Request Full Access Tell Your Colleague About Jove

6.13: SN1 Reaction: Stereochemistry

JoVE Core
Organic Chemistry

Ein Abonnement für JoVE ist erforderlich, um diesen Inhalt ansehen zu können. Melden Sie sich an oder starten Sie Ihre kostenlose Testversion.

SN1 Reaction: Stereochemistry

6.13: SN1 Reaction: Stereochemistry

This lesson provides an in-depth discussion of the stereochemical outcomes in an SN1 reaction.

In the first step of an SN1 reaction, the bond between the electrophilic carbon and the leaving group ionizes to generate the carbocation intermediate. The second step of the mechanism is the nucleophilic attack.

In the formed carbocation, the positively charged carbon is sp2 hybridized with a trigonal planar geometry. As all the three substituents lie on the same plane, a plane of symmetry for the carbocation is formed, making it achiral. Thus, a nucleophile can approach this symmetrical carbocation from either side with equal likelihood and rate.

The frontside attack leads to the retention of configuration, while a backside attack yields to an inversion of configuration in the product. However, in an achiral substrate, with either mode of attack, no difference in the product’s configuration is observed; in a chiral substrate, an optically inactive racemic mixture is expected.

Nevertheless, an enantiomeric excess with a predominantly inverted product is often observed because complete racemization cannot be achieved due to the ionization step. Upon ionization, the ions remain loosely associated, forming an intimate ion pair. During this period, the anion shields the carbocation from the frontside attack until they diffuse apart. Thus, the nucleophile is more prone to attack the unhindered backside resulting in products with an inversion of configuration. Once fully dissociated, both sides of the carbocation are available for substitution, and a racemic mixture of products is obtained. Thus, overall a net excess of inverted product is observed in an SN1 reaction.


SN1 Reaction Stereochemistry Electrophilic Carbon Leaving Group Carbocation Intermediate Nucleophilic Attack Sp2 Hybridized Trigonal Planar Geometry Achiral Plane Of Symmetry Frontside Attack Retention Of Configuration Backside Attack Inversion Of Configuration Optically Inactive Racemic Mixture Enantiomeric Excess

Get cutting-edge science videos from JoVE sent straight to your inbox every month.

Waiting X
Simple Hit Counter