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 freeQuestion: Cyclohex-2-enone has two protons on its carbon-carbon double bond (labeled Ha and Hb ) and two protons on the carbon adjacent to the double bond (labeled Hc ). (a) If Jab = 11 Hz and Jbc = 4 Hz, sketch the splitting pattern observed for each proton on the hybridized carbons. (b) Despite the fact that Ha is located adjacent to an electron-withdrawing C=O, its absorption occurs up-field from the signal due to Hb(6.0 vs. 7.0 ppm). Offer an explanation.
Question: How many \(^{\bf{1}}{\bf{H}}\) NMR signals would you expect for each compound?
a.
b.
c.
Question: Identify the structures of isomers E and F (molecular formula C4H802 ). Relative areas are given above each signal.
a.
b.
Which of the highlighted carbon atoms in each molecule absorbs farther downfield?
a.
b.
c.
d.
Question: A compound of molecular formula C4H802 shows no IR peaks at 3600–3200 or 1700 cm-1 . It exhibits one singlet in its 1H NMR spectrum at 3.69 ppm, and one line in its 13C NMR spectrum at 67 ppm. What is the structure of this unknown?
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