Chapter 9: Q65. (page 379)
Question: Draw the products of each reaction.
a.
b.
c.
d.
Short Answer
Answer
a
b.
c.
d.
Chapter 9: Q65. (page 379)
Question: Draw the products of each reaction.
a.
b.
c.
d.
Answer
a
b.
c.
d.
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Get started for freeQuestion: Draw a stepwise, detailed mechanism for the following reaction.
Question: Draw the product of each reaction.
a.
b.
Question: 1,2-Diols are converted to carbonyl compounds when treated with strong acids, in a reaction called the pinacol rearrangement.
(a) Draw a stepwise mechanism for this reaction. (Hint: The reaction proceeds by way of carbocation intermediates.)
(b) Assuming that the pinacol rearrangement occurs via the more stable carbocation, draw the rearrangement product formed from diol D.
Question: Give the structure corresponding to each name.
a. 7,7-dimethyloctan-4-ol
b. 5-methyl-4-propylheptan-3-ol
c. 2-tert-butyl-3-methylcyclohexanol
d. trans-cyclohexane-1,2-diol
Question: Give the IUPAC name for each compound.
a.
b.
c.
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