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
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
All the tools & learning materials you need for study success - in one app.
Get started for freeQuestion. Compound Q has molecular formula C5H9CIO2. Deduce the structure of P from its 1H and 13C -NMR spectra.
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?
Propose a structure for a compound of molecular formula C3H8O with an IR absorption at 3600 to 3200 cm-1 and the following NMR spectrum:
Question: How many \(^{\bf{1}}{\bf{H}}\) NMR signals would you expect for each compound?
a.
b.
c.
Which compounds give a 1H NMR spectrum with two signals in a ratio of 2:3?
a.
b.
c.
d.
What do you think about this solution?
We value your feedback to improve our textbook solutions.