Chapter 21: 46P (page 817)
Draw the products of each reaction.
a.
b.
c.
d.
e.
f.
g.
h.
Short Answer
a.
b.
c.
d.
e.
f.
g.
h.
Chapter 21: 46P (page 817)
Draw the products of each reaction.
a.
b.
c.
d.
e.
f.
g.
h.
a.
b.
c.
d.
e.
f.
g.
h.
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Get started for freeDraw all stereoisomers formed in each reaction.
a.
b.
c.
d.
Consider the para-substituted aromatic ketones, NO2C6H4COCH2 (p-nitroacetophenone) and CH3OC6H4COCH3 (p-methoxyacetophenone).
a. Which carbonyl compound is more stable?
b. Which compound forms the higher percentage of hydrate at equilibrium?
c. Which compound exhibits a carbonyl absorption at a higher wavenumber in its IR spectrum?
Explain your reasoning in each part.
Draw a stepwise mechanism for the following reaction
Give the structure corresponding to each name.
a. 2-methyl-3-phenylbutanal
b. 3,3-dimethylcyclohexanecarbaldehyde
c. 3-benzoylcyclopentanone
d. 2-formylcyclopentanone
e. (R)-3-methylheptan-2-one
f. m-acetylbenzaldehyde
g. 2-sec-butylcyclopent-3-enone
h. 5,6-dimethylcyclohex-1-enecarbaldehyde
Which carbonyl group in each pair absorbs at a higher frequency?
a.
b.
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