Chapter 9: Q40P (page 495)
Show how you would convert the following starting materials into the target compound. You may use any additional reagents you need.
Chapter 9: Q40P (page 495)
Show how you would convert the following starting materials into the target compound. You may use any additional reagents you need.
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Get started for free(a)Count the elements of unsaturation in cicutoxin, capillin, and panaxytriol.
(b) Draw structural formulas of at least two alkynes of each molecular formula.
(1) (2) (3)
The fragrance of (Z)-1-phenylhex-2-en-1-ol resembles that of roses, with a delicate citrus edge. Show how you would synthesize this compound from benzaldehyde (PhCHO) and any other reagents you need.
When pent-2-yne reacts with mercuric sulfate in dilute sulfuric acid, the product is a mixture of two ketones. Give the structures of these products, and use mechanisms to show how they are formed.
Predict the product(s) you would expect from the treatment of each compound with (1) dilute, neutral and (2) warm basic , then dilute acid.
(a) hex-1-yne (b) hex-2-yne (c) hex-3-yne
(d) 2-methylhex-3-yne (e) cyclodecyne
Question: Show how you might synthesize the following compounds, using acetylene and any suitable alkyl halides as your starting materials. If the compound given cannot be synthesized by this method, explain why. (a) hex-1-yne (b) hex-2-yne (c) hex-3-yne (d) 4-methylhex-2-yne (e) 5-methylhex-2-yne (f) cyclodecyne.
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