What can I do to prepare for organic chemistry lab?

1 Answer
Apr 9, 2015

First off, you need a reference text. This is my recommendation for a cheap, yet very helpful text.
http://www.amazon.com/Techniques-Organic-Chemistry-Microscale-Williamson/dp/1429219564/ref=sr_1_2?s=books&ie=UTF8&qid=1428564666&sr=1-2

This also acts as a great and free reference, if your compound has already been analyzed:
http://sdbs.db.aist.go.jp/sdbs/cgi-bin/cre_index.cgi

Then, you need to be able to recognize the types of peak shapes (sharp and strong, sharp and weak, broad and strong, etc.) and what they might represent. For example, an O-H stretching vibration at 3500~3200cm1 is often broad, like a bonding potential energy curve, and should be about medium or strong in a proper-concentration IR analyte solution. However, an N-H stretch potentially forms a more defined peak if it overlaps an O-H stretch in the same compound; it's less curved and a little more 'spiky'. (cf. 2-aminoethanol in SDBS.)

Some commonly recurring ones it helps to know/memorize/recognize, from Mohrig :
3650~3550cm1: O-H stretches (alcohols) -- non-H-bonded
Broad, generally medium
3550~3200cm1: O-H stretches (alcohols) -- H-bonded
Broad, generally strong
3550~3150cm1: N-H stretches (amides, amines)
Generally broad, medium; occasionally is more defined if overlapping O-H stretch
3310~3200cm1: C-H sp stretches
Generally strong
3100~3000cm1: C-H sp2 stretches (alkenes + aromatics)
Generally medium to weak
2990~2850cm1: C-H sp3 stretches
Generally medium to strong

~2360cm1: CO2 (doublet)
Generally quite weak

{1680~1620cm1: C=C stretches (saturated, alkene)
1650~1600cm1: C=C stretches (conjugated, alkene)
1620~1440cm1: C=C stretches (aromatics)}
Generally medium to weak
{1740~1720cm1: C=O aldehyde stretches (saturated)
1715~1680cm1: C=O aldehyde stretches (conjugated)}
Generally medium to weak
1750~1705cm1: C=O ketone stretches (saturated)
1700~1650cm1: C=O ketone stretches (conjugated)

1480~1430,1395~1340cm1: C-H sp3 bends