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Kasturi Talukdar

Updated on 01st July, 2023 , 6 min read

Lewis Base Examples, Applications, Properties and Reactions

Lewis Base Examples Overview

A Lewis base is a molecule or ion that has an electron pair available for sharing. It is also known as a nucleophile. In simple words, it is a substance that can donate its electron pair to form a covalent bond with another substance, which is known as a Lewis acid. The concept of Lewis bases was introduced by Gilbert N. Lewis in 1923, and it has proven to be of great importance in the field of chemistry. In this article, we will discuss various examples of Lewis bases and their applications.

Svante Arrhenius proposed the first acid-base theory in 1884, which describes acid as a substance that contains hydrogen or produces H+ in an aqueous solution, while bases are substances that contain hydroxyl groups or produce OH- in an aqueous solution. Johannes Nicolaus Bronsted and Thomas Martin Lowry independently proposed the Bronsted-Lowry theory of acid-base in 1923, where an acid donates protons, and a base accepts protons. In the same year, Gilbert N. Lewis proposed the Lewis acid and base theory, which is widely accepted and allows for the prediction of a wider variety of acid-base reactions.

Lewis Base Examples: Background

Gilbert Lewis, an American chemist, is credited with discovering the concept of bonding electron pairs and the acid-base theory named after him. After studying at Harvard University, he taught at Berkeley College for 34 years, where he contributed significantly to the development of the chemistry program. Although his primary area of research was thermodynamics, he published his work on electrons in 1913. He is also known for his contribution to the development of the Lewis dot structures that are still used today to symbolize the structure of atoms. Lewis was a crucial figure in the development of modern-day chemistry with his discovery of electrons and their properties.

Read More About:  Father of Chemistry.

Lewis Base Examples: Definition

A Lewis base is a substance that has an electron pair available for sharing. When a Lewis base donates an electron pair, it forms a coordinate covalent bond with a Lewis acid. Lewis bases are also known as nucleophiles since they are electron-rich species that seek out positively charged atoms or molecules to bond with.

Lewis Base Examples Possess the Ability to Donate an Electron Pair

The following are Lewis base examples of entities that possess the ability to donate an electron pair:

  • Pyridine and its derivatives have the capacity to donate electrons and are therefore categorized as Lewis bases.
  • Compounds containing Oxygen, Sulphur, Selenium, and Tellurium from group 16 of the Periodic Table, exhibiting an oxidation state of -2, can function as Lewis bases. Water and ketones are some examples of such compounds.
  • Simple anions that possess an electron pair, like H- and F-, can donate electrons and hence act as Lewis bases. Additionally, some complex anions like the sulfate anion (SO42-) also have electron-pair-donating abilities.
  • π-systems that are rich in electrons, such as benzene, ethyne, and ethene, possess excellent electron-pair-donating capabilities.
  • Weak Lewis acids are accompanied by strong conjugate Lewis bases. Additionally, numerous chemical species that contain a lone pair of electrons, like CH3- and OH-, can be identified as Lewis bases owing to their electron-pair-donating capabilities.

Lewis Base Examples to Form a Covalent Bond 

Lewis bases are substances that have a lone pair of electrons, which they can donate to form a coordinate covalent bond with a Lewis acid. The following are Lewis base examples:

  1. Neutral Lewis Bases:Neutral Lewis bases are molecules that have a lone pair of electrons, making them good electron donors. Some examples of neutral Lewis bases include:
  2. Ammonia (NH3): Ammonia is a colorless gas with a pungent smell. It is widely used as a fertilizer and in the production of various chemicals.
  3. Water (H2O): Water is a transparent, tasteless, and odorless liquid. It is the most common substance on Earth and is essential for all forms of life.
  4. Carbon monoxide (CO): Carbon monoxide is a toxic gas that is produced by the incomplete combustion of fossil fuels. It is used as a reducing agent in the extraction of metals from their ores.
  5. Anionic Lewis Bases:Anionic Lewis bases are negatively charged ions that have a lone pair of electrons. Some examples of anionic Lewis bases include:
  6. Fluoride ion (F-): Fluoride ion is an anion that is commonly found in toothpaste and mouthwash. It is used to prevent tooth decay.
  7. Hydroxide ion (OH-): Hydroxide ion is an anion that is formed when water loses a proton. It is commonly found in basic solutions and is used to neutralize acids.
  8. Cyanide ion (CN-): Cyanide ion is a toxic anion that is commonly used in the mining industry to extract gold and other precious metals.
  9. Cationic Lewis Bases:Cationic Lewis bases are positively charged ions that can act as electron donors. Some examples of cationic Lewis bases include:
  10. Ammonium ion (NH4+): Ammonium ion is a cation that is formed when ammonia accepts a proton. It is commonly found in fertilizers and is essential for plant growth.
  11. Silver-ammonia complex ion (Ag (NH3)2+): This complex ion is formed when silver ions react with ammonia. It is used in photography and in the production of mirrors.
  12. Copper-ammonia complex ion (Cu (NH3)42+): This complex ion is formed when copper ions react with ammonia. It is used in electroplating and in the production of dyes and pigments.

Lewis Base Examples: Applications

Lewis bases have many important applications in chemistry, particularly in the fields of catalysis, synthesis, and materials science. Here are some examples of their applications:

  1. Metal Coordination and Complexation: Many Lewis bases, especially those with multiple donor atoms, can coordinate with metals and form stable complexes. These complexes have important applications in catalysis, especially in asymmetric catalysis, where chiral Lewis bases are used to modify the selectivity and activity of metallic catalysts.
  2. Chelating Agents: Certain Lewis bases, such as ethylenediamine and diethylenetriamine, can form multiple bonds with a single metal ion, a property known as chelation. This property makes them useful as chelating agents, which are widely used in various industrial and agricultural applications, such as water treatment, mineral extraction, and crop protection.
  3. Lewis Base Catalysis: In addition to modifying the properties of metal catalysts, Lewis bases can also act as catalysts. For example, Lewis base catalysis has been used in the synthesis of many important organic compounds, such as pharmaceuticals and natural products.
  4. Molecular Recognition and Binding: Many Lewis bases have the ability to recognize and selectively bind to certain molecules, such as metal ions or organic molecules. This property makes them useful in various applications, such as sensors, drug delivery, and molecular separation.
  5. Polymerization: Lewis bases have also been used in polymerization reactions, where they act as initiators or co-catalysts. For example, Lewis bases such as triethylaluminium have been used in the Ziegler-Natta polymerization of olefins to produce high-quality polymers with well-defined structures.

Read more about Formal Charge Formula and Electrophilic Substitute Reaction

Lewis Base Examples in Daily Life Applications

Lewis Base

Application in Everyday Life

Ammonia

Household cleaning products such as window and floor cleaners

Water

Used as a solvent, coolant, and reactant in many chemical reactions

Oxygen

Essential for respiration in living organisms

Carbonate ions

Used in antacid medications to neutralize stomach acid

Hydroxide ions

Used in drain cleaners and oven cleaners

Nitrate ions

Used in fertilizers for plants

Acetate ions

Used in food additives and flavorings

Sulfur dioxide

Used in the production of paper and in preserving wine

Ethylene glycol

Used as a coolant in car engines

Chloride ions

Used as a disinfectant in swimming pools

Carbon dioxide

Used in carbonated drinks and in fire extinguishers

Lewis Base Examples: Chemical Reactions between Lewis Acids and Bases 

  1. Lewis acids accept a pair of electrons from Lewis bases.
  2. The reaction results in the formation of a coordinate covalent bond between the acid and base.
  3. The Lewis acid gains a negative charge, and the Lewis base gains a positive charge.
  4. The Lewis acid acts as an electron acceptor, while the Lewis base acts as an electron donor.
  5. The acid-base interaction leads to the formation of a complex ion, which is stabilized by electrostatic forces of attraction.
  6. The strength of the Lewis acid-base interaction depends on the electronegativity and size of the atoms involved.
  7. The reaction is reversible, and the complex ion can dissociate to reform the Lewis acid and base.
  8. Lewis acids and bases can catalyze a variety of chemical reactions, including organic synthesis and polymerization reactions.

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Frequently Asked Questions

A Lewis base is a chemical species that has a lone pair of electrons and can donate these electrons to a Lewis acid to form a coordinate covalent bond.

Examples of Lewis bases include ammonia (NH3), water (H2O), pyridine (C5H5N), and fluoride ion (F-).

Lewis acids and bases involve the transfer of electrons, while Bronsted-Lowry acids and bases involve the transfer of protons.

A chelating agent is a multidentate Lewis base that can form multiple coordinate covalent bonds with a Lewis acid. Ethylenediamine (en) and diethylenetriamine (dien) are examples of chelating agents.

The Lewis symbol for a Lewis base is the chemical symbol for the element or molecule, followed by a pair of dots to represent the lone pair of electrons.

A Lewis base bonds with a Lewis acid by donating its lone pair of electrons to an empty orbital on the Lewis acid, forming a coordinate covalent bond.

Lewis bases are generally polar compounds with high electron density and high boiling points. They can also form hydrogen bonds and have the ability to solvate cations.

Lewis bases are used as ligands in organometallic chemistry, as reagents in organic synthesis, and as catalysts in various chemical reactions.

Yes, Lewis bases can act as nucleophiles by donating a pair of electrons to an electrophilic center in a chemical reaction.

While all nucleophiles are Lewis bases, not all Lewis bases are nucleophiles. Nucleophiles are specifically defined as chemical species that can donate an electron pair to an electrophilic center, while Lewis bases have a more general definition of donating a pair of electrons to a Lewis acid.

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