
Acidity and Electron-Withdrawing Groups
Interactive Video
•
Chemistry
•
10th - 12th Grade
•
Hard

Jackson Turner
FREE Resource
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10 questions
Show all answers
1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the effect of adding a fluorine atom to acetic acid?
It increases the pKa value.
It decreases the acidity.
It makes the hydroxyl group more acidic.
It has no effect on acidity.
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
How does the inductive effect influence the stability of the conjugate base?
It has no effect on the base.
It destabilizes the base by increasing its positive charge.
It increases the negative charge on the base.
It stabilizes the base by reducing its negative charge.
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which halogen is more effective as an electron-withdrawing group?
Iodine
Bromine
Fluorine
Chlorine
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the pKa value of fluoroacetic acid?
4.75
2.7
2.9
3.0
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
How does the proximity of an electron-withdrawing group affect acidity?
Further proximity increases acidity.
Closer proximity decreases acidity.
Closer proximity increases acidity.
Proximity has no effect on acidity.
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the pKa value of 2-bromo pentanoic acid compared to 3-bromo pentanoic acid?
Lower
Higher
Not comparable
The same
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which factor does NOT affect the acidity of a molecule?
Color of the molecule
Type of electron-withdrawing group
Proximity of the electron-withdrawing group
Number of electron-withdrawing groups
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