Q8 P-c
Question
Question:Using any alkyne needed, how would you prepare the following alkenes?
(c) 3-Methyl-1-pentene
Step-by-Step Solution
Verified Answer
1Step-by-Step Solution Step1: Lindlar catalyst
It’s the reagent used in the react to convert the akyne to alkene by hydrogenation when 1 equivalent When 2equivalent is present alkyne convert to alkane.
2Step2: Formation ofcis-3-Heptene
Alkyne hydrogenation to alkene occurs when less active Lindlar catalyst is used which is a finely divided palladium metal with lead acetate and quinoline, an aromatic amine. The hydrogenation occurs with syn stereochemistry
3Step3: Reaction with lindlar catalyst
When alkyne react with lindlar catalyst then it break the three out of one bond and convert alkyne to alkene by the addition of hydrogen to the atom and form alkene as shown:
Other exercises in this chapter
Q9-7P b
How would you prepare the following carbonyl compounds starting from an alkyne (reddish-brown Br)?b.
View solution Q. 9-9-8 P-b
Using any alkyne needed, how would you prepare the following alkenes? (b) cis-3-Heptene
View solution Q. 9-9-8 P-c
Using any alkyne needed, how would you prepare the following alkenes? (c) 3-Methyl-1-pentene
View solution Q9-9P a
The of acetone, pkaof acetone, CH3COCH3 is 19.3. Which of the following bases is strong enough to deprotonate acetone?(a) KOH (pka of H2O 1
View solution