Chapter 14: Q.21558-14-7P. (page 535)
How many NMR signals would you expect for each compound?
a.
b.
c.
Short Answer
a. 4
b. 5
c. 5
Chapter 14: Q.21558-14-7P. (page 535)
How many NMR signals would you expect for each compound?
a.
b.
c.
a. 4
b. 5
c. 5
All the tools & learning materials you need for study success - in one app.
Get started for freeQuestion: Rank the highlighted carbon atoms in each compound in order of increasing chemical shift.
a.
b.
Question: (a) How many 1H NMR signals does each compound show? (b) Into how many peaks is each signal split?
Question. Compound Q has molecular formula C5H9CIO2. Deduce the structure of P from its 1H and 13C -NMR spectra.
Question: Explain why the 13C NMR spectrum of 3-methylbutan-2-ol shows five signals.
Question: Identify the structures of isomers A and B (molecular formula C9H10O ).
Compound A: IR peak at 1742 cm-1 ; 1 H NMR data (ppm) at 2.15 (singlet, 3 H), 3.70 (singlet, 2 H), and 7.20 cm-1(broad singlet, 5 H). Compound B: IR peak at 1688 ; 1 H NMR data (ppm) at 1.22 (triplet, 3 H), 2.98 (quartet, 2 H), and 7.28–7.95 (multiplet, 5 H).
What do you think about this solution?
We value your feedback to improve our textbook solutions.