Chapter 13: Q 1. (page 499)
Question: What is the mass of the molecular ion formed from compounds having each molecular formula:
(a) ; (b);(c); (d) methamphetamine ?
Short Answer
Answer
a. 58
b. 140
c. 136
d. 149
Chapter 13: Q 1. (page 499)
Question: What is the mass of the molecular ion formed from compounds having each molecular formula:
(a) ; (b);(c); (d) methamphetamine ?
Answer
a. 58
b. 140
c. 136
d. 149
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Get started for freeQuestion:Propose two possible structures for a hydrocarbon having an exact mass of 96.0939 that forms ethylcyclopentane upon hydrogenation with H2 and Pd-C.
Question:2,3-Dimethylbutane and 2,2-dimethylbutane have the same molecular ion in the mass spectrum, but only one of these isomers gives a significant fragment at m/z= 57.
(a) Whichisomer shows an intense peak at m/z= 57?
(b) Propose a structure for the ion that gives riseto this peak.
(c) The base peak in the mass spectrum of the other isomer occurs at m/z= 43.
What ion gives rise to this peak?
Question:Propose four possible structures for a hydrocarbon with a molecular ion at m/z= 112.
Oxidation of citronellol, a constituent of rose and geranium oils, with PCC in the presence of added NaOCOCH3 forms compound A. A has a molecular ion in its mass spectrum at 154 and a strong peak in its IR spectrum at 1730 cm-1. Without added NaOCOCH3, oxidation of citronellol with PCC yields isopulegone, which is then converted to B with aqueous base. B has a molecular ion at 152, and a peak in its IR spectrum at 1680 cm-1.
a. Identify the structures of A and B.
b. Draw a mechanism for the conversion of citronellol to isopulegone.
c. Draw a mechanism for the conversion of isopulegone to B.
Question: Match each compound to its IR spectrum.
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