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Ethylidene chloride is

Short Answer

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Ethylidene chloride, also known as 1,1-dichloroethane, is an organochloride compound with the chemical formula C₂H₄Cl₂. Its chemical structure can be represented as: Cl-C(Cl)-C(H)(H). This colorless liquid has a sweet odor and is primarily used as a chemical intermediate and an industrial solvent. It has applications in industries such as packaging and textile manufacturing, automotive, and aerospace. Note that the compound is toxic and should be handled with proper safety precautions.

Step by step solution

01

Identify Ethylidene Chloride

Ethylidene chloride, also known as 1,1-dichloroethane, is an organochloride compound with the chemical formula C₂H₄Cl₂. It is a colorless liquid with a sweet odor. Now, we will draw its chemical structure.
02

Draw the Chemical Structure

To draw the chemical structure of ethylidene chloride (1,1-dichloroethane), follow these steps: 1. Draw a two carbon atoms in a horizontal row and label them C. These represent the two carbon atoms in the compound. 2. Draw a single bond between the two carbon atoms. 3. Attach two chlorine atoms to the first carbon atom using single bonds and label them Cl. These represent the two chlorine atoms in the compound. 4. Attach two hydrogen atoms to the second carbon atom using single bonds and label them H. These represent the remaining two hydrogen atoms in the compound. Your final structure should look like this: ``` Cl H | | Cl-C - C-H ```
03

Properties and Applications

Ethylidene chloride (1,1-dichloroethane) has a boiling point of 57.2°C and a density of 1.235 g/mL. It is slightly soluble in water and miscible with most organic solvents. The compound is used primarily as a chemical intermediate and an industrial solvent. Some common applications of ethylidene chloride include: 1. As a solvent for resins, waxes, and fats in industries like packaging and textile manufacturing. 2. As an intermediate in the production of other chemicals, such as vinyl acetate and ethyleneamines. 3. As a strong and effective cleaning agent for metal surfaces in the automotive and aerospace industries. 4. In the past, it was used as a refrigerant and as an aerosol propellant, but due to its environmental impact and negative effects on human health, these uses have been largely phased out. Please keep in mind that the compound is toxic and prolonged exposure may cause harmful effects on human health. Always handle and work with ethylidene chloride in a well-ventilated area and follow proper safety precautions.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Chemical Structure of Ethylidene Chloride
Understanding the chemical structure of ethylidene chloride, also known as 1,1-dichloroethane, is crucial for students as they delve into the study of organochlorides. To visualize ethylidene chloride, picture a molecule with two carbon atoms linked by a single bond (C-C). Attached to the first carbon atom are two chlorine atoms, and the second carbon atom bears two hydrogen atoms. The atoms connect with single bonds, leading to a structural formula of Cl2CH-CH3.

This structure represents a relatively simple organic molecule but embodies important aspects of chemical bonding, such as the sharing of electrons indicative of single covalent bonds. Recognizing this molecular framework paves the way to appreciate the reactivity and interactions of ethylidene chloride, especially when dealing with substitutions and the formation of additional compounds in organic chemistry.
Properties of Ethylidene Chloride
Ethylidene chloride's properties are tied closely to its molecular structure. The molecule is a colorless liquid at room temperature, with a characteristic sweet aroma that can be a signal of its presence. It displays a moderate boiling point of 57.2°C, which factors into how it reacts under different temperature conditions.

Due to its density of 1.235 g/mL, it is heavier than water, which affects how it can be separated in a mixture. The compound's solubility traits show slight water solubility but an excellent ability to mix with most organic solvents. Such physical properties are important considerations when ethylidene chloride is used in various industrial applications, influencing how it can be stored, transported, and utilized in manufacturing processes. Despite its use, it is essential to acknowledge the toxic nature of ethylidene chloride, necessitating adherence to safety protocols and protective measures during its handling.
Applications of Ethylidene Chloride
Ethylidene chloride serves multiple roles across various industries, with its chemical stability and solvent power being instrumental. It's most commonly employed as a solvent for waxes, fats, and resins, particularly in industries like textiles and packaging. The compound's role in the manufacturing of vinyl acetate and ethyleneamines showcases its utility as a chemical intermediate.

In the realm of metal cleaning, ethylidene chloride shines due to its effectiveness in degreasing and preparing surfaces in the automotive and aerospace sectors. Although its use as a refrigerant and aerosol propellant has considerably diminished due to environmental and health concerns, its impact on these industries is historical.

Notably, when discussing applications, it's vital to pair the information with the necessary safety precautions. Prolonged exposure to ethylidene chloride has detrimental effects on health. Therefore, always highlight the importance of operating in well-ventilated areas and complying with safety guidelines to ensure the well-being of those working with this chemical.

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Most popular questions from this chapter

Which compound produces only one alkene when treated with sodium methoxide? (A) 2 -chloro-2-methylpentane (B) 3 -chloro-3-ethylpentane (C) 3 -chloro-2-methylpentane (D) 2 -chloro-4-methylpentane

Which statement is not correct? (A) Pure Alkyl bromides are colourless (B) Alkyl bromides and iodides develop colour when exposed to light (C) \(\mathrm{R}-\mathrm{CN}\) is obtained as a major product on reaction between \(\mathrm{R}-\mathrm{X}\) and \(\mathrm{AgCN}\) (D) \(\mathrm{R}-\mathrm{NO}_{2}\) is obtained as a major product on reaction between \(\mathrm{R}-\mathrm{X}\) and \(\mathrm{AgNO}_{2}\)

In the following reactions: (a) \(\mathrm{CH}_{2}=\mathrm{CH}-\mathrm{CH}_{3} \stackrel{\mathrm{NCS}}{\longrightarrow}\) (b) \(\mathrm{CH}_{2}^{14}=\mathrm{CH}-\mathrm{CH}_{2}-\mathrm{OH} \stackrel{\mathrm{soCl}_{2}}{\longrightarrow}\) If \(\mathrm{CH}_{2}^{14}=\mathrm{CH}-\mathrm{CH}_{2}-\mathrm{Cl}\) is \(\mathrm{P}\) and \(\mathrm{CH}_{2}=\mathrm{CH}-\mathrm{CH}_{2} \mathrm{Cl}\) is \(\mathrm{Q}\), then major product obtained is (A) Pin both reaction (B) P in reaction (a) and \(\mathrm{Q}\) in reaction (b) (C) P in reaction (b) and Q in reaction (a) (D) \(\mathrm{P}, \mathrm{Q}\) in reaction (a) and \(\mathrm{Q}\) in reaction (b)

In an elimination reaction, Hoffmann product dominates over Sytzeff product if : (A) Leaving tendency of leaving group is poor (B) Bulkier base is used (C) Higher stability of hoffmann product over Sytzeff product (D)All

The compound which shows higher rate of \(S_{N} 1\) as well as \(S_{N} 2\) mechanism than \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{Cl}\) is (A) \(\mathrm{CH}_{3}-\mathrm{Cl}\) (B) \(\mathrm{CH}_{3}-\mathrm{NH}-\mathrm{CH}_{2} \mathrm{Cl}\) (C) \(\mathrm{CHO}-\mathrm{CH}_{2} \mathrm{Cl}\) (D) \(\left(\mathrm{CH}_{3}\right)_{3} \mathrm{C}-\mathrm{Cl}\)

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