Chapter 13: Q 33. (page 522)
Question:What cations are formed in the mass spectrometer by α cleavage of each of the following compounds?
Short Answer
Answer
Chapter 13: Q 33. (page 522)
Question:What cations are formed in the mass spectrometer by α cleavage of each of the following compounds?
Answer
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Get started for freeQuestion:A chiral compound Y has a strong absorption at 2970–2840 in its IR spectrum and gives the following mass spectrum. Propose a structure for Y.
Question: The carbonyl absorption of an amide typically occurs in the 1630–1680 cm-1 range, while the carbonyl absorption of an ester occurs at much higher wavenumber, typically 1735–1745 cm-1 . Account for this difference.
Question: What major IR absorptions are present above 1500 for each compound?
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: The low-resolution mass spectrum of an unknown analgesic X had a molecular ion of 151. Possible molecular formulas include , , and . High-resolution mass spectrometry gave an exact mass of 151.0640. What is the molecular formula of X?
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