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 free4-Methyl-2-pentanone and 3-methylpentanal are isomers. Explain how
you could tell them apart, both by mass spectrometry and by infrared
spectroscopy.
Question: Grignard reagents undergo a general and very useful reaction with
ketones. Methylmagnesium bromide, for example, reacts with cyclohexanoneto yield a product with the formula . What is the structure of this product if it has an IR absorption at ?
Nonconjugated ,-unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated ,-unsaturated isomers. Propose a mechanism for this isomerization.
Assign CahnโIngoldโPrelog rankings to the following sets of substituents
a.
b.
c.
d.,
How would you prepare the following substances, starting from any
compounds having four carbons or fewer?
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