Dear students,
This is a tutorial
on reading IR spectra to make your preparation for the exam complete. I take
the opportunity to discuss the IR question from the previous quiz.
Here is the
spectrum given in the quiz:
You were
asked to choose between two compounds, C
and D as to which the spectrum
belongs to. C is an aldehyde (1-pentanal)
and D is a carboxylic acid
(pentanoic acid).
Let’s look
closely at the spectrum. The most obvious peak is the intense and sharp
carbonyl (C=O) stretch at 1727 cm-1 signalling the presence of a
carbonyl which both compounds have in common, both are carbonyl compounds. Next,
look closer at a moderately intense peak at 2719 cm-1. There are
actually two peaks at ~ 2700 and ~2800 cm-1, one of the peaks being
half hidden behind the bigger saturated C-H stretch bands. This two peaks show
the presence of C-H stretch of an aldehyde. So, this is
clear indication that this spectrum belongs to compound C.
Some of you
may have been misled by a rather medium size peak at around 3500 cm-1.
This is NOT an O-H stretch. It is
probably an overtone of our intense carbonyl band at ~1700 cm-1. If you remember the IR spectrum
of myristic acid from our Nugmeg myristicin practical, you will see that the
O-H stretch band of myristic acid is distinctively different: it is broader,
smooth, and spreads over a larger region (overlapping the saturated C-H bands).
Have a look at it again.
An actual IR
spectrum of compound D, pentanoic
acid (it’s also called valeric acid) is shown below:
Hope this
little discussion clears the haze regarding IR spectrum.
I include
here a video on reading IR spectra (a substitute tutorial teacher ) that I find useful for your
preparation. Pleasant viewing and good luck for the exams.
Source: Youtube channel Sarutahiko1
(www.youtube.com/watch?v=XIWc9eT476c)
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