Chapter 9: Q. 9-9-8 P-c (page 274)
Using any alkyne needed, how would you prepare the following alkenes?
(c) 3-Methyl-1-pentene
Chapter 9: Q. 9-9-8 P-c (page 274)
Using any alkyne needed, how would you prepare the following alkenes?
(c) 3-Methyl-1-pentene
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Get started for freeA hydrocarbon of unknown structure has the formula C8H10. On catalytic hydrogenation over the Lindlar catalyst, 1 equivalent of H2 is absorbed. On hydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed.
(a) How many degrees of unsaturation are present in the unknown structure?
(b) How many triple bonds are present?
(c) How many double bonds are present?
(d) How many rings are present?
(e) Draw a structure that fits the data.
The following cycloalkyne is too unstable to exist. Explain
Question: How would you carry out the following reactions?
Draw structures corresponding to the following names:
(a)3,3-Dimethyl-4-octyne
(b)3-Ethyl-5-methyl-1,6,8-decatriyne
(c)2,2,5,5-Tetramethyl-3-hexyne
(d)3,4-Dimethylcyclodecyne
(e)3,5-Heptadien-1-yne
(f)3-Chloro-4,4-dimethyl-1-nonen-6-yne
(g)3-sec-Butyl-1-heptyne
(h)5-tert-Butyl-2-methyl-3-octyne
Propose structures for hydrocarbons that give the following products
on oxidative cleavage by KMnO4 or O3 :
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