Chapter 21: 14P (page 817)
Draw the products of each reaction. Include all stereoisomers formed
a.
b.
Short Answer
a.
b.
Chapter 21: 14P (page 817)
Draw the products of each reaction. Include all stereoisomers formed
a.
b.
a.
b.
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Get started for freeGive the IUPAC name for each compound.
a.
b.
c.
d.
e.
f.
Give the structure corresponding to each name:
(a) sec-butyl ethyl ketone
(b) methyl vinyl ketone
(c) p-ethylacetophenone
(d) 3-benzoyl-2-benzylcyclopentanone
(e) 6,6-dimethylcyclohex-2-enone
(f) 3-ethylhex-5-enal
An unknown compound C of molecular formula C6H12O3 exhibits a strong absorption in its IR spectrum at 1718 cm-1 and the given 1H NMR spectrum. What is the structure of C?
Show two methods to synthesize each alkene: a one-step method using a Wittig reagent, and a two-step method that forms a carbonโcarbon bond with an organometallic reagent in one of the steps.
a.
b.
Treatment of (HOCH2CH2CH2CH2)2CO with acid forms a product of molecular formula C9H16O2and a molecule of water. Draw the structure of the product and explain howit is formed.
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