Chapter 14: Q.21558-14-48P (page 563)
Question: How many 13C NMR signals do each compound exhibit?
Short Answer
Answer
a. Five
b. Three
c. Seven
d. Three
e. Seven
f. Five
g. Four
h. Three
Chapter 14: Q.21558-14-48P (page 563)
Question: How many 13C NMR signals do each compound exhibit?
Answer
a. Five
b. Three
c. Seven
d. Three
e. Seven
f. Five
g. Four
h. Three
All the tools & learning materials you need for study success - in one app.
Get started for freeHow many signals are present in the 1HNMR spectrum for each molecule? What splitting is observed in each signal?
a.
b.
c.
Into how many peaks will each proton shown in green be split?
a.
b.
c.
d.
e.
f.
Question:Answer the following questions about each of the hydroxy ketones: 1-hydroxybutan-2-one (A) and 4-hydroxybutan-2-one (B).
a. What is the molecular ion in the mass spectrum?
b. What IR absorptions are present in the functional group region?
c. How many lines are observed in the 13C NMR spectrum?
d. How many signals are observed in the 1H NMR spectrum?
e. Give the splitting observed for each type of proton as well as its approximate chemical shift.
Question: Explain why the carbonyl carbon of an aldehyde or ketone absorbs farther downfield than the carbonyl carbon of an ester in a 13C NMR spectrum
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?
What do you think about this solution?
We value your feedback to improve our textbook solutions.