For each compound, show the products obtained from ozonolysis, followed by treatment with dimethyl sulfide.
d.
For each compound, show the products obtained from ozonolysis, followed by treatment with dimethyl sulfide.
d.
For each compound, show the products obtained from ozonolysis, followed by treatment with dimethyl sulfide.
c.
What is the major product of each of the following reactions?
f.
What hydrocarbon forms the following products after reaction first with ozone and then with dimethyl sulfide?
Give structures of the alkenes that would give the following products upon ozonolysis–reduction.
(b)
Give structures of the alkenes that would give the following products upon ozonolysis–reduction.
(a)
Give the products expected when the following compounds are ozonized and reduced.
(c)
(d)
Give the products expected when the following compounds are ozonized and reduced.
(a)
(b)
Limonene is one of the compounds that give lemons their tangy odor. Show the structures of the products expected when limonene reacts with an excess of each of these reagents.
(c) ozone, then dimethyl sulfide
Predict the major products of the following reactions.
(a) (E)-3-methyloct-3-ene + ozone, then (CH3)2S
When compound Z is treated with ozone, followed by dimethyl sulfide and washing with water, the products are formic acid, 3-oxobutanoic acid, and hexanal.
Propose a structure for compound Z. What uncertainty is there in the structure you have proposed?
Draw the product(s) you'd expect when each of these alkenes is treated first with O3, then with CH3SCH3
(a)
Formation of the molozonide can be expected to proceed stereospecifically. Why is this the case? Show the two different molozonides you would expect to get from ozonolysis of (E)- and (Z)-3,4-dimethylhept-3-ene.
In Solved Assessment 9.30(b), we came up with an alkene that under the conditions of ozonolysis would produce acetophenone and acetaldehyde. There is one other alkene that should produce the same compounds under these conditions. Which is it?
Suggest a synthesis of the following aldehydes or ketones using the ozonolysis reaction of an alkene.
(a)