What determines the formation of different elimination products in a reaction?

Elimination Reactions and Alkene Stability

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Chemistry
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11th - 12th Grade
•
Hard

Amelia Wright
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10 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
The concentration of the reactants
The type of solvent used
The temperature of the reaction
Which beta proton is extracted by the base
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
How is the Zaitsev product defined in terms of alkene substitution?
It is always the least substituted alkene
It is the alkene with the least carbon atoms
It is the more highly substituted alkene
It is the alkene with the most hydrogen atoms
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which alkene is considered more stable?
Unsubstituted alkene
Monosubstituted alkene
Tetrasubstituted alkene
Disubstituted alkene
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the thermodynamically favored product in an elimination reaction?
The more stable, highly substituted alkene
The product with the highest energy
The product formed fastest
The product with the least steric hindrance
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which base would likely lead to a higher proportion of the Hoffman product?
Ethoxide
Tert-butoxide
Methoxide
Hydroxide
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Why might a sterically hindered base favor the Hoffman product?
It reacts with the solvent
It forms the most stable product
It has a lower activation energy for certain protons
It can easily access all protons
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which product is formed when the base is sterically unhindered?
The most substituted alkene
The least stable product
The least substituted alkene
The fastest forming product
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