
Organocuprates in Organic Synthesis
Interactive Video
•
Chemistry
•
11th - 12th Grade
•
Practice Problem
•
Hard
Aiden Montgomery
FREE Resource
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10 questions
Show all answers
1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What qualifies organocuprates as organometallic reagents?
They are similar to Grignard reagents.
They contain copper.
They are prepared from organolithium reagents.
They are used in SN2 reactions.
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the role of copper in the preparation of organocuprates?
It acts as a catalyst.
It is used to neutralize the reaction.
It forms a central anion with alkyl groups.
It replaces lithium in the reaction.
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the significance of the lithium counter ion in organocuprates?
It forms a complex with copper.
It acts as a reducing agent.
It participates in the reaction.
It stabilizes the copper anion.
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
How do organocuprates differ from Grignard reagents in their reactivity?
They are more reactive.
They do not react with carbonyls.
They are less reactive and softer.
They react with different functional groups.
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
In a conjugate addition reaction, where do organocuprates attack?
Gamma position of a ketone.
Carbonyl carbon.
Beta position of an alpha-beta unsaturated ketone.
Alpha position of a ketone.
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the primary purpose of using organocuprates in synthetic strategies?
To perform 1,2-addition reactions.
To attach alkyl groups at the beta position of carbonyls.
To form Grignard reagents.
To reduce carbonyl compounds.
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the result of the conjugate addition of organocuprates to an alpha-beta unsaturated ketone?
Formation of a new carbonyl group.
Creation of a new double bond.
Removal of the alpha-beta unsaturation.
Formation of a Grignard reagent.
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