We’re being asked to determine the product of the given reaction.
Recall that alcohols are converted to alkenes via POCl3 dehydration, which is carried out using POCl3 in pyridine and occurs in two steps:
(1) nucleophilic attack + deprotonation – the –OH group attacks POCl3 via SN2. The intermediate is immediately deprotonated by pyridine, which is a base.
(2) E2 β-elimination – pyridine removes a β-hydrogen via E2
Which of the following is the product of the following reaction?
Frequently Asked Questions
What scientific concept do you need to know in order to solve this problem?
Our tutors have indicated that to solve this problem you will need to apply the POCl3 Dehydration concept. You can view video lessons to learn POCl3 Dehydration. Or if you need more POCl3 Dehydration practice, you can also practice POCl3 Dehydration practice problems.
How long does this problem take to solve?
Our expert Organic tutor, Jonathan took 2 minutes and 20 seconds to solve this problem. You can follow their steps in the video explanation above.