Chapter 14: Q.21558-14-14P. (page 546)
Into how many peaks will each proton shown in green be split?
a.

b.

c.

d.

e.

f.

Short Answer
a. 3 and 4
b. 2 and 4
c. 1, 3, and 3
d. 2 and 2
e. 2 and 2
f. 2 and 3
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Chapter 14: Q.21558-14-14P. (page 546)
Into how many peaks will each proton shown in green be split?
a.

b.

c.

d.

e.

f.

a. 3 and 4
b. 2 and 4
c. 1, 3, and 3
d. 2 and 2
e. 2 and 2
f. 2 and 3
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Question: Identify the structures of isomers H and I (molecular form C8H11N)
a.

b.

Question: 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: What splitting pattern is observed for each proton in the following compounds?
a.

b.

Question. Treatment of butan-2-one (CH3COCH2CH3) with a strong base followed by CH3l forms a compound Q, which gives a molecular ion in its mass spectrum at 86. The IR (> 1500 only) and 1H-NMR spectrum of Q is given below. What is the structure of Q?

Question: For each compound, which of the protons on the highlighted carbons absorbs farther downfield?
a. 
b. 
c. 
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