Chapter 12: Q13P (page 354)
Show how you could prepare the following compounds from 4-methyl-3- penten-2-one,
(a)
(b)
(c)
Short Answer
(a)
Formation of the desired product
(b)
Formation of the desired product
(c)
Formation of the desired product
Chapter 12: Q13P (page 354)
Show how you could prepare the following compounds from 4-methyl-3- penten-2-one,
(a)
(b)
(c)
(a)
Formation of the desired product
(b)
Formation of the desired product
(c)
Formation of the desired product
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Get started for freeThe infrared spectrum of the compound with the mass spectrum shown below has strong absorbances at 1584, 1478, and 1446 cm-1 . Propose a
structure consistent with the data.
Camphor, a saturated monoketone from the Asian camphor tree, is used among other things as a moth repellent and as a constituent of embalmingfluid. If camphor has M+=152.1201 by high-resolution mass spectrometry,what is its molecular formula? How many rings does camphor have?
Question: Where might the following compounds have IR absorptions?
Question: At what approximate positions might the following compounds showIR absorptions?
(e)
Assuming that strong acids add to alkynes in the same manner as they add to alkenes, propose a mechanism for each of the following reactions:
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