Chapter 14: Q5P (page 527)
Question: How many \(^{\bf{1}}{\bf{H}}\) NMR signals does each compound give?
a.
b.
c.
d.
Short Answer
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Chapter 14: Q5P (page 527)
Question: How many \(^{\bf{1}}{\bf{H}}\) NMR signals does each compound give?
a.
b.
c.
d.
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Get started for freeQuestion: Propose a structure consistent with each set of data.
a. A compound X (molecular formula C6H12O2) gives a strong peak in its IR spectrum at 1740 cm-1. The 1 H NMR spectrum of X shows only two singlets, including one at 3.5 ppm. The 13C NMR spectrum is given below Propose a structure for X.
b. A compound Y (molecular formula C6H10 ) gives four lines in its 13C NMR spectrum (27, 30, 67, and 93 ppm), and the IR spectrum given here. Propose a structure for Y.
Draw a splitting diagram for Hb in trans-1,3-dichloropropene, given that Jab = 13.1 Hz and Jbc = 7.2 Hz.
Label each statement as True or False.
a. When a nucleus is strongly shielded, the effective field is larger than the applied field and the absorption shifts downfield.
b. When a nucleus is strongly shielded, the effective field is smaller than the applied field and the absorption is shifted upfield.
c. A nucleus that is strongly deshielded requires a lower field strength for resonance.
d. A nucleus that is strongly shielded absorbs at a larger δ value.
Which of the highlighted carbon atoms in each molecule absorbs farther downfield?
a.
b.
c.
d.
Question: Label the protons in each highlighted \({\bf{C}}{{\bf{H}}_{\bf{2}}}\) group as enantiotopic, diastereotopic, or homotopic.
a.
b.
c.
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