How is diethyl ether prepared from ethyl bromide and ethyl alcohol?

Answer 1

#"Diethyl ether"# from #"ethyl bromide.........."#?

What about "ethyl alcohol" and "ethyl bromide" along with a small amount of non-nucleophilic base?

#"H"_3"CCH"_2"Br" + "HOCH"_2"CH"_3 stackrel("base")rarr "H"_3"CCH"_2"OCH"_2"CH"_3+"base"*"HBr"#

Naturally, you need to locate a helpful base.

Given the product's volatility and flammability, there would definitely be effective industrial preparation, carried out under very strict guidelines.

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Answer 2

Diethyl ether can be prepared from ethyl bromide and ethyl alcohol through an acid-catalyzed dehydration reaction. The reaction proceeds as follows:

[ \text{C}_2\text{H}_5\text{Br} + \text{C}_2\text{H}_5\text{OH} \xrightarrow{\text{H}_2\text{SO}_4} \text{C}_2\text{H}_5\text{OC}_2\text{H}_5 + \text{HBr} ]

Here, sulfuric acid (( \text{H}_2\text{SO}_4 )) serves as the catalyst for the reaction, leading to the formation of diethyl ether (( \text{C}_2\text{H}_5\text{OC}_2\text{H}_5 )) and hydrogen bromide (( \text{HBr} )).

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Answer from HIX Tutor

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

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