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The Sn2 substitution, nucleophilic, bimolecular reaction

The abbreviation Sn2 conveys the information sub-stitution-nucleophilic-bimolecular . The reaction is essentially the displacement of one group, a leaving group, by another group, a nucleophile. It is a bimolecular reaction, since kinetic data indicate that two species are involved in the rate-determining step  [Pg.183]

Differences in electronegativities (see Section 2.7) between carbon and the leaving group atom lead to bond polarity. This confers a partial positive charge on the carbon and facilitates attack of the nucleophile. As the nucleophile electrons are used to make a new bond to the carbon, electrons must be transferred away to a suitable acceptor in order to maintain carbon s octet. The suitable acceptor is the electronegative leaving group. [Pg.183]

Essentials of Organic Chemistry Paul M De wick 2006 John Wiley Sons, Ltd [Pg.183]

The rate of an Sn2 reaction depends upon several variables. These are  [Pg.184]


See other pages where The Sn2 substitution, nucleophilic, bimolecular reaction is mentioned: [Pg.183]    [Pg.185]    [Pg.189]   


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Bimolecular nucleophilic

Bimolecular nucleophilic substitution

Bimolecular reactions substitution

Nucleophiles bimolecular substitution

Nucleophiles substitution reactions

Nucleophilic substitution reactions nucleophiles

SN2-nucleophiles

Sn2 nucleophilic substitution reaction

Sn2 nucleophilicity

Sn2 reactions nucleophiles

Sn2 substitution

Sn2 substitution reactions

Substitution bimolecular

Substitution reactions nucleophile

Substitution reactions nucleophilic

Substitution reactions nucleophilic, bimolecular

The Nucleophile

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