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Ch. 14 - Ethers, Epoxides, and Thioethers
Wade - Organic Chemistry 9th Edition
Wade9th EditionOrganic ChemistryISBN: 9780135213728Not the one you use?Change textbook
Chapter 14, Problem 23

Cellosolve® is the trade name for 2-ethoxyethanol, a common industrial solvent. This compound is produced in chemical plants that use ethylene as their only organic feedstock. Show how you would accomplish this industrial process.

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Step 1: Begin with ethylene (C₂H₄) as the organic feedstock. Ethylene is a simple alkene with a double bond between two carbon atoms.
Step 2: Perform an epoxidation reaction on ethylene to convert it into ethylene oxide (oxirane). This can be achieved using a peracid, such as m-chloroperoxybenzoic acid (mCPBA), or other suitable oxidizing agents.
Step 3: React ethylene oxide with ethanol (C₂H₅OH) in the presence of an acid catalyst, such as sulfuric acid (H₂SO₄), to open the epoxide ring and form 2-ethoxyethanol. The acid catalyst facilitates the nucleophilic attack of ethanol on the epoxide ring.
Step 4: Purify the product mixture to isolate 2-ethoxyethanol. This can involve distillation or other separation techniques to remove impurities and unreacted starting materials.
Step 5: Confirm the structure and purity of 2-ethoxyethanol using analytical techniques such as nuclear magnetic resonance (NMR) spectroscopy or gas chromatography (GC).

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Ethanol and Ethylene Chemistry

Ethanol (C2H5OH) is a simple alcohol that can be derived from ethylene (C2H4) through a hydration reaction. This process involves the addition of water to ethylene in the presence of an acid catalyst, resulting in the formation of ethanol. Understanding this reaction is crucial for producing 2-ethoxyethanol, as it serves as a precursor in the synthesis.
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Ether Formation

2-Ethoxyethanol is classified as an ether, specifically an ethyl ether. Ethers are formed through the reaction of alcohols with alkyl halides or through the condensation of two alcohol molecules. In the case of 2-ethoxyethanol, the reaction involves the nucleophilic attack of ethanol on an ethylene oxide intermediate, leading to the formation of the ether bond.
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Industrial Synthesis Processes

Industrial synthesis processes often utilize continuous flow reactors and catalytic methods to optimize yield and efficiency. In the production of 2-ethoxyethanol, controlling reaction conditions such as temperature, pressure, and catalyst type is essential to maximize the conversion of ethylene and minimize by-products. Understanding these industrial practices is vital for scaling up the synthesis from laboratory to production levels.
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Related Practice
Textbook Question

Propose mechanisms for the epoxidation and ring-opening steps of the epoxidation and hydrolysis of trans-but-2-ene shown above. Predict the product of the same reaction with cis-but-2-ene.

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Textbook Question

The 2001 Nobel Prize in Chemistry was awarded to three organic chemists who have developed methods for catalytic asymmetric syntheses. An asymmetric (or enantioselective) synthesis is one that converts an achiral starting material into mostly one enantiomer of a chiral product. K. Barry Sharpless (The Scripps Research Institute) developed an asymmetric epoxidation of allylic alcohols that gives excellent chemical yields and greater than 90% enantiomeric excess.

The Sharpless epoxidation uses tert-butyl hydroperoxide, titanium(IV) isopropoxide, and a dialkyl tartrate ester as the reagents. The following epoxidation of geraniol is typical.

(a) Which of these reagents is most likely to be the actual oxidizing agent? That is, which reagent is reduced in the reaction? What is the likely function of the other reagents?

(b) When achiral reagents react to give a chiral product, that product is normally formed as a racemic mixture of enantiomers. How can the Sharpless epoxidation give just one nearly pure enantiomer of the product?

(c) Draw the other enantiomer of the product. What reagents would you use if you wanted to epoxidize geraniol to give this other enantiomer?

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Textbook Question

Predict the major product when each reagent reacts with ethylene oxide.

(a) NaOCH2CH3 (sodium ethoxide)

(b) NaNH2 (sodium amide)

(c) NaSPh (sodium thiophenoxide)

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Textbook Question

Show how you would accomplish the following transformations. Some of these examples require more than one step.

(e) 2-chlorohexan-1-ol → 1,2-epoxyhexane

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Textbook Question

Show the rest of the mechanism for formation of the cyclized intermediate in Figure 14-6.

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Textbook Question

Predict the major product when each reagent reacts with ethylene oxide.

(d) PhNH2 (aniline)

(e) KCN (potassium cyanide)

(f) NaN3 (sodium azide)

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