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:
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Get started for freeWhat is the major product of the reaction of 1 mol of propyne with each of the following reagents?
a.HBr (1 mol)
b.HBr (2 mol)
c.Br2(1 mol)/CH2Cl2
d.Br2 (2 mol)/CH2Cl2
e.aqueous H2SO4, HgSO4
f.R2BH in THF followed byH2O2/HO- /H2O
g.excess H2, Pd/C
h.H2/Lindlar catalyst
i.sodium amide
j.the product of part i followed by1-chloropropane
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
Name the following:
Describe the alkyne you would start with and the reagents you would use if you wanted to Synthesize
a. Pentane. b. Cis-2-butene. c. trans-2-pentene. d. 1-hexene.
For each of the following alkynes, draw the products obtained from (1) the acid-catalyzed addition of water
(mercuric ion is added for part a) and from (2) hydroboration–oxidation:
a. 1-butyne b. 2-butyne c. 2-pentyne
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