Yahoo Answers is shutting down on May 4th, 2021 (Eastern Time) and the Yahoo Answers website is now in read-only mode. There will be no changes to other Yahoo properties or services, or your Yahoo account. You can find more information about the Yahoo Answers shutdown and how to download your data on this help page.
3 Answers
- Anonymous7 years agoFavorite Answer
Hi,
These take practice to get good at, if you're on the path to chemistry.
Looking at the top picture of your IR, that giant peak around 1700 cm-1 is a carbonyl stretch if you didn't know that already. And it looks like you have a pattern between the 1100-1300 that suggests an ester group.
Looking at your H-NMR I would infer you have three carbons with hydrogens on them. Hopefully you know how splitting patterns arise. The giant peak I assume has an integration of about 3 hydrogens, which would indicate a lone methyl group CH3. Now your peak around 1.25 suggests an ethyl group of CH2, and the peak at about 4.1 is another methyl group CH3. These two peaks are coupling with each other and you could check the J-value to confirm.
So in my mind I'm thinking: Lone methyl group, ester group, ethyl group, and another methyl group.
CH3-C00-CH2-CH3
This is the structure of ethyl acetate. Which fits the data.
You can also use a helpful site called SDBS to confirm structures and obtain spectrums for the compounds.
Hope this helps!
Source(s): Chemistry Major / Pre-Health Student - ?Lv 47 years ago
"Spectrometric Identification of Organic Compounds" By
Silverstein, Bassler, Morrill
need better pictures
- Anonymous7 years ago
and now your just spamming asking it a bunch