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21. Aldehydes and Ketones: Nucleophilic Addition - Part 6 of 7!
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21. Aldehydes and Ketones: Nucleophilic Addition - Part 6 of 7!
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21. Aldehydes and Ketones: Nucleophilic Addition / Thioacetal / Problem 5
Problem 5
Why is BF3 used instead of Bronsted Lowry acids in thioacetal formation?
A
BF3 has a higher boiling point than Bronsted Lowry acids.
B
BF3 is less reactive than Bronsted Lowry acids.
C
BF3 is a Lewis acid that can accept electron pairs, unlike Bronsted Lowry acids which donate protons.
D
BF3 is cheaper and more readily available than Bronsted Lowry acids.
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