Substitution reaction

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SN1 Reaction Mechanism
SN2 reaction mechanism
General Scheme for Base Catalyzed Nucleophilc Acyl Substitution
Electrophilic aromatic substitution
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Substitution reaction is a fundamental concept in organic chemistry involving the replacement of an atom or a group of atoms in a molecule with another atom or group of atoms. Substitution reactions are ubiquitous in organic synthesis and are critical for the creation of a vast array of chemical compounds, ranging from pharmaceuticals to polymers.

Types of Substitution Reactions[edit | edit source]

Substitution reactions can be broadly classified into two main types based on the nature of the attacking species: nucleophilic substitution and electrophilic substitution.

Nucleophilic Substitution (S_N)[edit | edit source]

In a nucleophilic substitution reaction, a nucleophile, which is a species rich in electrons, attacks an electron-deficient carbon atom, leading to the replacement of a leaving group (usually a halogen or a similar electronegative group). Nucleophilic substitution reactions can be further divided into two mechanisms: S_N1 and S_N2.

S_N1 Reaction[edit | edit source]

The S_N1 mechanism involves two steps: the formation of a carbocation intermediate by the departure of the leaving group, followed by the attack of the nucleophile. S_N1 reactions are unimolecular, involving a first-order rate equation, and are favored in tertiary and some secondary alkyl halides.

S_N2 Reaction[edit | edit source]

The S_N2 mechanism is a one-step process where the nucleophile attacks the substrate at the same time as the leaving group departs. This reaction involves a backside attack, leading to an inversion of configuration at the carbon center. S_N2 reactions are bimolecular, with a second-order rate equation, and are favored in primary and some secondary alkyl halides.

Electrophilic Substitution (S_E)[edit | edit source]

In an electrophilic substitution reaction, an electrophile, which is a species deficient in electrons, attacks an electron-rich site on the molecule, typically in aromatic systems. This type of reaction is prevalent in the chemistry of benzene and its derivatives, where the electrophile replaces a hydrogen atom on the aromatic ring.

Mechanism and Factors Influencing Substitution Reactions[edit | edit source]

The mechanism of substitution reactions depends on various factors, including the nature of the substrate, the leaving group, the nucleophile or electrophile, and the solvent. The rate of the reaction can be influenced by the strength and stability of the nucleophile or electrophile, the leaving group's ability to leave, and the solvent's ability to stabilize the transition state or intermediates.

Applications[edit | edit source]

Substitution reactions are widely used in the synthesis of a variety of chemical products, including pharmaceuticals, agrochemicals, and materials. They are essential for the modification of molecular structures, the introduction of functional groups, and the construction of complex molecules in organic synthesis.

See Also[edit | edit source]

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