CHEM 353 Tutorial MS & IR
CHEM 353 Tutorial MS & IR
KNUST
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CHEM 353
Organic Synthesis and Spectroscopy
Tutorials
Lecturer: Dr. Clement Osei Akoto
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2. The reaction of (Z)-2-pentene with water and a trace of H2SO4 forms two products. Identify
the products from their mass spectra.
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3. The mass spectrum of 2-methyl-3-pentanol is shown below.
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4. Point out which of these four mass spectra indicate the presence of sulfur, chlorine, bromine,
iodine, or nitrogen. Suggest a molecular formula for each.
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5. Account for the peaks at m/z 87, 111, and 126 in the mass spectrum of 2,6-dimethylheptan-
4-ol.
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1. Identify the compound that gives the mass spectrum and infrared spectrum shown here.
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2. The IR spectrum of a compound with molecular formula C5H8O is shown below. Identify
the compound.
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3. Which one of the following five compounds produced the IR spectrum shown below?
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4. Each of the IR spectra shown below is accompanied by a set of four compounds. In each
case, indicate which of the four compounds is responsible for the spectrum.
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5. Five compounds are shown for each of the IR spectra below. Indicate which of the five
compounds is responsible for each spectrum.
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