Problem 8
Question
Distillation of diethyl ether to dryness may cause explosion. The reason is that (a) It is very volatile (b) It is very unstable (c) It polymerizes on heating to form an explosive compound (d) It may contain ether hydroperoxide formed by autooxidation which decomposes very rapidly on heating
Step-by-Step Solution
Verified Answer
The danger lies in option (d): the presence of ether hydroperoxide from autooxidation.
1Step 1: Understanding Diethyl Ether Properties
Diethyl ether, also known as ethoxyethane, is a highly volatile and flammable liquid. It is commonly used as a solvent in laboratories. However, when exposed to air, it forms peroxides over time, some of which can be explosive.
2Step 2: Analyze the Options
Carefully examine the given options:
(a) suggests high volatility, which contributes to flammability but not instability.
(b) indicates instability, though diethyl ether is generally stable unless certain conditions (like peroxides formation) occur.
(c) talks about polymerization, which is not a known characteristic of diethyl ether.
(d) refers to the formation of ether hydroperoxide due to autooxidation, which is a known issue, and these peroxides are highly explosive.
3Step 3: Identifying the Correct Explanation
While diethyl ether is indeed volatile, the key safety concern associated with it is the potential formation of ethers hydroperoxides. Autooxidation occurs when it is exposed to air and this leads to the formation of peroxides, which can explode upon heating and distillation.
4Step 4: Selecting the Best Option
Based on the understanding developed from analyzing each option, choice (d) accurately explains why distilling diethyl ether to dryness can be dangerous. The formation of ether hydroperoxides is specifically what leads to the risk of explosion.
Key Concepts
Understanding Volatile SolventsPeroxide Formation and Its DangersExploring AutooxidationEnsuring Laboratory Safety with Diethyl Ether
Understanding Volatile Solvents
Volatile solvents are liquids that easily evaporate at room temperature. This is primarily due to their low boiling points. In a laboratory setting, chemicals like diethyl ether fall into this category. Their volatility implies that they can quickly fill a space with flammable vapors. This increases the likelihood of fire or explosion if an ignition source is present.
- Diethyl ether is highly volatile, with a boiling point of just 34.6°C.
- The rapid evaporation rate means that it can easily mix with air, creating a highly flammable mixture.
- This underlines the need for proper ventilation when working with such solvents.
Peroxide Formation and Its Dangers
Peroxide formation in volatile solvents like diethyl ether occurs when these chemicals are exposed to air for extended periods. This leads to the slow oxidation of the solvent, resulting in hydroperoxide compounds. These peroxides are dangerous:
- Over time, the concentration of peroxides can reach dangerous levels.
- These compounds are sensitive to shock, heat, and friction, which can cause them to detonate unexpectedly.
- Regular testing and disposal of old solvent bottles are necessary to prevent the buildup of peroxides.
Exploring Autooxidation
Autooxidation is a process where a substance like diethyl ether reacts with oxygen in the air. This reaction occurs naturally over time without the need for external catalysts and can lead to the formation of explosive peroxides.
- This is a concerning feature of many ether-containing solvents.
- It generally starts slowly but can accelerate as peroxide levels increase.
- Limiting exposure to air by storing solvents in tightly sealed containers can minimize autooxidation.
Ensuring Laboratory Safety with Diethyl Ether
Laboratory safety involving volatile and potentially explosive solvents like diethyl ether requires stringent practices and precautions:
- Adequate ventilation is essential to disperse any vapors that might accumulate.
- Always store diethyl ether in well-sealed, peroxide-free containers.
- Regularly check for the presence of peroxides using test strips or indicators.
- Dispose of outdated chemicals following proper hazardous waste protocols.
Other exercises in this chapter
Problem 6
The \(\mathrm{C}-\mathrm{O}\) - C bond angle in the ether molecule is (a) \(180^{\circ}\) (b) \(150^{\circ}\) (c) \(90^{\circ}\) (d) \(110^{\circ}\)
View solution Problem 7
The major product obtained on the monobromination (with \(\mathrm{Br}_{2} / \mathrm{FeBr}_{3}\) ) of the following compound isCOc1cccc(C)c1 (a) Cc1cccc(O)c1Br (
View solution Problem 9
Reaction between sodium cthoxide and bromoethane gives (a) methyl ethyl ether (b) Dimethyl ether (c) Diethyl ether (d) propane
View solution Problem 10
The number of ethers pussitile with the molecular formula \(C_{4} H_{10} O\) is (a) Che (b) Iwo (c) Three (d) Four
View solution