
Stereochemistry and Reaction Pathways

Interactive Video
•
Chemistry
•
11th - 12th Grade
•
Hard

Mia Campbell
FREE Resource
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10 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the starting material for the practice problem discussed in the video?
A ketone
A dihalide
An alkyne
An alkene
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which reaction is primarily discussed as a method to obtain vicinal dihalides?
Hydration
Dihalogenation
Hydrogenation
Oxidation
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the stereochemical outcome when converting an alkyne to an E alkene using sodium and ammonia?
Cis configuration
Trans configuration
Random configuration
No change in configuration
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which reagent is used to achieve the E alkene from an alkyne?
H2 with Pd/C
Sodium and ammonia
Lindlar's catalyst
Br2 in CCl4
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Why is bond rotation important in achieving the desired stereochemistry in dihalogenation?
To increase reaction speed
To align the molecules for better reactivity
To achieve the correct stereochemical outcome
To prevent side reactions
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the purpose of rotating the bond 180 degrees in the stereochemical discussion?
To decrease the reaction time
To increase the reaction temperature
To achieve a more familiar conformation
To change the molecular formula
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which catalyst is used to convert an alkyne to a Z alkene?
H2 with Pd/C
Br2 in CCl4
Lindlar's catalyst
Sodium and ammonia
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