Chapter 12: 13P (page 354)
Question: What alkyl halides would you use to prepare the following ketones by an acetoacetic ester synthesis?
Chapter 12: 13P (page 354)
Question: What alkyl halides would you use to prepare the following ketones by an acetoacetic ester synthesis?
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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.
How might you use IR spectroscopy to distinguish between the followingpairs of isomers?
(a) CH3 CH2 OH and CH3 OCH3
(b) Cyclohexane and 1 - hexene
(c) CH3 CH2 CO2 H and HOCH2 CH2 CHO
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 ?
The mercury-catalyzed hydration of alkynes involves the formation of an organomercury enol intermediate. Draw the electron-pushing mechanism to show how each of the following intermediates is formed.
Identify each pair of relationships among the groups in glucose (pink–blue, pink–dark blue, pink–black, blue–dark blue, blue-black, dark blue-black) as cis or trans.
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