Chapter 7: Q14P (page 301)
What ketones would be formed from the acid-catalyzed addition of water to 3-heptyne?
Short Answer
R-C≡C-R' + H₂O → R-CH₂-CO-R' + R-CO-CH₂-R'
As here unsymmetrical alkyne is there so two ketones will form:
Chapter 7: Q14P (page 301)
What ketones would be formed from the acid-catalyzed addition of water to 3-heptyne?
R-C≡C-R' + H₂O → R-CH₂-CO-R' + R-CO-CH₂-R'
As here unsymmetrical alkyne is there so two ketones will form:
All the tools & learning materials you need for study success - in one app.
Get started for freeName the following:
Which alkyne would be the best one to use for the synthesis of each of the following ketones?
Which of the following pairs are keto–enol tautomers?
Draw a condensed structure for each of the following:
a.2-hexyne
b.5-ethyl-3-octyne
c.methylacetylene
d.vinylacetylene
e.methoxyethyne
f.sec-butyl-tert-butylacetylene
g.1-bromo-1-pentyne
h.5-methyl-2-cyclohexenol
i.diethylacetylene
j.di-tert-butylacetylene
k.cyclopentylacetylene
l. 5,6-dimethyl-2-heptyne
Draw the mechanism for the following reaction
What do you think about this solution?
We value your feedback to improve our textbook solutions.