Chapter 14: Q.21558-14-9P. (page 538)
For each compound, first label each different type of proton and then rank the protons in order of increasing chemical shift.
a.
b.
c.
Short Answer
a.
b.
c.
Chapter 14: Q.21558-14-9P. (page 538)
For each compound, first label each different type of proton and then rank the protons in order of increasing chemical shift.
a.
b.
c.
a.
b.
c.
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Get started for freeWhat protons in alcohol A give rise to each signal in its 1HNMR spectrum? Explain all splitting patterns observed for absorptions between 0–7 ppm.
Question: Draw the structure of a compound of molecular formula C4H8O that has a signal in its 13C NMR spectrum at > 160 ppm. Then draw the structure of an isomer of molecular formula C4H80 that has all of its 13C NMR signals at < 160 ppm.
Propose a structure consistent with each set of data.
a. C9H10O2: IR absorption at 1718cm-1
b. C9H12 : IR absorption at 2850–3150cm-1
How many peaks are present in the NMR signal of each labelled proton?
a.
b.
c.
d.
Compound A exhibits two signals in its 1H NMR spectrum at 2.64 and 3.69 ppm and the ratio of the absorbing signals is 2:3. Compound B exhibits two signals in its 1H NMR spectrum at 2.09 and 4.27 ppm and the ratio of the absorbing signals is 3:2. Which compound corresponds to dimethyl succinate and which compound corresponds to ethylene diacetate?
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