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i have to give a reason for that and suggest the trough(if formed) is likley to be broadened.

2007-10-06 04:46:36 · 1 answers · asked by Anonymous in Science & Mathematics Chemistry

1 answers

Yes!!!!

The keto - group (C=O)in the ester linkage will produce a very strong absorption at approximately 1740 cm^-1. An absorption in the range 1680 - 1750 cm^-1 is very characteristic of the keto group (C=O) in any molecule. It is usually shown as a very narrow 'spike'.
The C-O part of the ester produces an absorption in the range 1000 - 1300 cm^-1, but this usually is a series of absorptions, and not a broadening.
The hydroxy group (O-H) in alcohols produces are broad absorption in the range 3230 - 3550 cm^-1
The hydroxy group (O-H) in acids produces a very characteristic broad absorption in the range 2500 -3000 cm^-1.
As ethyl ethanoate is an ester it does not have any hydroxy groups present, so it will not produce a broad signal.

2007-10-06 06:26:46 · answer #1 · answered by lenpol7 7 · 0 0

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