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what does the structure of triethylamine look like when reacting with ether. it is soluble.

because the N in the triethylamine does NOT have a hydrogen attached to it, it just has 2 electrons, i dont understand how it reacts with ether? will it take a hydrogen molecule from one of the carbons in the ether?

PLEASE HELP

2007-09-13 08:01:50 · 1 answers · asked by Anonymous in Science & Mathematics Chemistry

1 answers

Triethylamine doesn't react with ether. There are no places where each could donate its nonbonding electrons to the other in a Lewis acid-base reaction, for example. And as you point out, there is no exchangeable N-H.

2007-09-13 08:14:09 · answer #1 · answered by steve_geo1 7 · 0 0

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