Practicing Success

Target Exam

CUET

Subject

Chemistry

Chapter

Organic: Alcohols, Phenols and Ethers

Question:

What is the solvent nature of ethers?

Options:

They are bad solvents

They are excellent solvents

They are average solvents

They cannot act as solvents

Correct Answer:

They are excellent solvents

Explanation:

The correct answer is option 2. They are excellent solvents.

Let us delve into why ethers are considered excellent solvents by looking at their chemical properties and behavior as solvents:

Polarity and Solubility

Moderate Polarity:

Ethers have an oxygen atom bound to two alkyl or aryl groups. The oxygen is more electronegative than carbon, creating a dipole moment. However, ethers are less polar compared to alcohols or water. This moderate polarity allows ethers to dissolve a variety of substances, including many organic compounds.

Solvent Capabilities:

Ethers can dissolve both polar and non-polar substances, which makes them versatile solvents. They are particularly good at dissolving organic compounds that do not dissolve well in water. For example, diethyl ether can dissolve hydrocarbons, esters, and other organic compounds that are less soluble in water.

Non-Reactivity

Inertness:

Ethers are relatively chemically inert under normal conditions. This means they do not easily react with many chemicals, which is advantageous when using them as solvents in reactions. They do not participate in many chemical reactions themselves, which helps prevent unwanted side reactions.

Hydrogen Bonding

Limited Hydrogen Bonding:

Ethers can engage in hydrogen bonding with substances that have hydrogen bond donors (such as alcohols), though they do not form hydrogen bonds as strongly as alcohols or water. This limited hydrogen bonding ability still contributes to their effectiveness as solvents for compounds that do not have strong hydrogen bonding interactions.

Boiling Points

Moderate Boiling Points:

Ethers generally have lower boiling points compared to alcohols and many other organic solvents. This is due to the lack of strong intermolecular hydrogen bonding in ethers. Their relatively low boiling points make them useful as solvents in reactions where a lower boiling point is desirable. For example, diethyl ether boils at around 34.6°C, and tetrahydrofuran (THF) boils at around 66°C.

Practical Examples

Diethyl Ether: Historically used as a common solvent in laboratories for extractions and reactions. Its low boiling point and ability to dissolve many organic compounds made it a staple solvent.

Tetrahydrofuran (THF): A versatile solvent used in various organic synthesis processes and industrial applications. THF has a higher boiling point and can dissolve a wide range of polar and non-polar substances.

Summary

Ethers are considered excellent solvents because:

They dissolve a broad range of organic compounds, including those that are not soluble in water. They are chemically inert and do not react with many chemicals, reducing the risk of side reactions. Their moderate polarity and boiling points make them useful in various chemical processes.

Therefore, ethers are valued in chemistry for their solvent properties and practical utility in many laboratory and industrial applications.