Chapter 17: Q14P (page 552)
What alcohols would give the following products on oxidation?
(a)
(b)
(c)
Short Answer
a.
b.
c.
Chapter 17: Q14P (page 552)
What alcohols would give the following products on oxidation?
(a)
(b)
(c)
a.
b.
c.
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What products would you obtain from reaction of 1-pentanol with thefollowing reagents?
(a)
(b)
(c)
(d) Dess- Martin periodinane
The conversion of 3° alcohols into alkenes under acidic conditions involves two cationic intermediates. For each reaction, draw the complete mechanism using curved arrows.
(a)
(b)
(c)
Use the reaction of a Grignard reagent with a carbonyl compound to synthesize the following compound:
Question:Reaction of (S)-3-methyl-2-pentanone with methyl magnesium bromide followed by acidification yields 2,3-dimethyl-2-pentanol. What is the stereochemistry of the product? Is the product optically active?
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