(a) When ethylene oxide is treated with anhydrous HBr gas, the major product is 1,2-dibromoethane. When ethylene oxide is treated with concentrated aqueous HBr, the major product is ethylene glycol. Use mechanisms to explain these results.

(b) Under base-catalyzed conditions, several molecules of propylene oxide can react to give short polymers. Propose a mechanism for the base-catalyzed formation of the following trimer.

Short Answer

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a)

b)

Step by step solution

01

Acid-catalyzed ring opening of epoxides

Epoxides react under both acidic and basic conditions. The products of the acid-catalyzed ring opening depend primarily on the solvent used.

02

Base catalyzed ring opening of epoxides

Epoxides are considered to be more reactive since opening the epoxide ring relieves the strain of the three-membered ring. Strong bases can attack and open epoxides, even though the leaving group is an alkoxide. Amines can also open epoxides.

03

Synthesis

(a) Ethylene oxide on treatment with anhydrous HBr gas, forms 1,2-dibromoethane as the major product.

ethylene oxide 1,2-dibromoethane

the reaction of ethylene oxide with anhydrous HBr

Ethylene oxide on treatment with concentrated aqueous HBr, forms ethylene glycol as the major product.


ethylene oxide ethylene glycol

the reaction of ethylene oxide with concentrated HBr

(b) Strong bases can attack and open epoxides.

Formation of trimer from propylene oxide molecule

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Most popular questions from this chapter

An acid-catalyzed reaction was carried out using methyl cellosolve (2-methoxyethanol) as the solvent. When the 2-methoxyethanol was redistilled, a higher-boiling point fraction (bp 162oC) was also recovered. The mass spectrum of this fraction showed the molecular weight to be 134. The IR and NMR spectrum are shown here. Determine the structure for this compound and propose a mechanism for its formation.

There are two ways of making 2-ethoxyoctane from octan-2-ol using the Williamson ether synthesis. When pure (-) -octan-2-ol of specific rotation -8.240is treated with sodium metal and then ethyl iodide, the product is 2-ethoxyoctane with a specific rotation of -15.60. When pure (-) -octan-2-ol is treated with tosyl chloride and pyridine and then with sodium ethoxide, the product is also 2-ethoxyoctane. Predict the rotation of the 2-ethoxyoctane made using the tosylation/sodium ethoxide procedure, and propose a detailed mechanism to support your prediction.

Boron tribromide(BBr3)cleaves ethers to give alkyl halides and alcohols.

The reaction is thought to involve attack by a bromide ion on the Lewis acid-base adduct of the ether with(BBr3)(a strong Lewis acid). Propose a mechanism for the reaction of butyl methyl ether with(BBr3)to give (after hydrolysis) butan-1-ol and bromomethane.

A compound of molecular formula C8H8Ogives the IR and NMR spectra shown here. Propose a structure and show how it is consistent with the observed absorptions.

(a) Tetramethyloxirane is too hindered to undergo nucleophilic substitution by the hindered alkoxide, potassium tert-butoxide. Instead, the product is the allylic alcohol shown. Propose a mechanism to explain this reaction. What type of mechanism does it follow?

(b) Under mild acid catalysis, 1,1-diphenyloxirane undergoes a smooth conversion to diphenylethanal (diphenylacetaldehyde). Propose a mechanism for this reaction. (Hint: Think Pinacol.)

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