
Retrosynthetic Analysis in Organic Chemistry

Interactive Video
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Chemistry
•
11th Grade - University
•
Hard

Amelia Wright
FREE Resource
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10 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the primary goal of retrosynthetic analysis in synthetic chemistry?
To create new molecules from scratch
To break down complex molecules into simpler starting materials
To analyze the physical properties of molecules
To determine the molecular weight of compounds
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
In retrosynthetic analysis, what does the arrow represent?
A physical transformation
The undoing of a reaction
A change in molecular weight
A chemical reaction
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which reaction is commonly used to form alcohols in retrosynthetic analysis?
Friedel-Crafts reaction
Grignard reaction
Diels-Alder reaction
Wittig reaction
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the role of PCC in the retrosynthetic analysis of alcohols?
To convert alcohols to ketones
To oxidize alcohols to aldehydes
To reduce alcohols to alkanes
To form ethers from alcohols
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which reaction is used to form alkenes in retrosynthetic analysis?
Friedel-Crafts reaction
Grignard reaction
Wittig reaction
Diels-Alder reaction
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
In the Wittig reaction, what is the role of the ylide?
To oxidize the substrate
To reduce the substrate
To act as a nucleophile
To form a new carbon-carbon double bond
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is a key feature of the Diels-Alder reaction in retrosynthetic analysis?
It oxidizes alkenes to alcohols
It rearranges three pi bonds into a pi bond and two sigma bonds
It reduces ketones to alcohols
It forms a new carbon-carbon single bond
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