

Organic Chemistry: Nucleophiles, Electrophiles, and Intermediates
Interactive Video
•
Chemistry
•
11th - 12th Grade
•
Practice Problem
•
Hard
Jennifer Brown
FREE Resource
10 questions
Show all answers
1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What are the main roles of nucleophiles and electrophiles in organic reaction mechanisms?
Nucleophiles donate protons, electrophiles accept protons.
Nucleophiles and electrophiles both donate protons.
Nucleophiles donate electron pairs, electrophiles accept electron pairs.
Nucleophiles accept electron pairs, electrophiles donate electron pairs.
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
In a nucleophilic attack, what does the nucleophile do?
It forms a bond with another nucleophile.
It donates a proton to an electrophile.
It forms a bond with an electrophile.
It accepts an electron pair from an electrophile.
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which of the following is true about strong nucleophiles?
They are typically neutral.
They lack lone pairs of electrons.
They often have a negative charge.
They usually have a positive charge.
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What makes alkyl halides good electrophiles?
They are always positively charged.
They can break off to allow nucleophiles to bond.
They can easily donate electrons.
They have a high electronegativity.
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which of the following is NOT a common electrophile?
Carbonyl
Carbocation
Nucleophile
Alkyl halide
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the trend in stability for carbocations?
Primary > Secondary > Tertiary
Tertiary > Secondary > Primary
Methyl > Tertiary > Primary
Secondary > Tertiary > Methyl
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
How does hyperconjugation affect carbocation stability?
It decreases stability by increasing electron deficiency.
It increases stability by donating electron density.
It has no effect on stability.
It increases stability by removing electron density.
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