Free Radical Halogenation
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Chemistry, Science
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11th Grade - University
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Easy
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7 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the initiation step in radical halogenation?
Combination of two radicals
Dissociation of a molecule into radicals
Formation of a stable molecule
Formation of a covalent bond
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
During the propagation step, what happens when a chlorine radical interacts with methane?
It forms a stable methane molecule
It results in a hydrogen radical
It creates a methyl radical and HCl
It produces a chlorine molecule
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is a potential outcome of further chlorination of a monochlorinated product?
Formation of a single product
Creation of a dichlorinated product
No further reaction
Formation of a stable alkane
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Why is it important to consider stereochemistry in radical mechanisms?
Radicals are always non-reactive
Radicals form only one type of product
Radicals can lead to racemic mixtures
Radicals do not affect stereochemistry
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is a key difference between bromination and chlorination in terms of regioselectivity?
Bromination is less regioselective
Chlorination is more regioselective
Bromination is more regioselective
Both are equally regioselective
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Why is bromine more regioselective than chlorine in halogenation?
Chlorine radicals are more stable
Bromine is smaller than chlorine
Bromine radicals are less stable
Bromine can better accommodate instability
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What happens when a chlorine radical collides with a molecule during chlorination?
It forms a stable alkane
It extracts any available hydrogen
It creates a stable chlorine molecule
It forms a bromine radical
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