🤓 Based on our data, we think this question is relevant for Professor Howitz's class at UCI.
We’re being asked to draw the product for the given reaction sequence.
Recall that the hydroxyl group can be converted into a good leaving group using sulfonyl chlorides, which follows an SN2 mechanism:
Write the structural formula of the main organic product for the following reaction between an alcohol, tosyl chloride, and then a nucleophile.
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 Leaving Group Conversions - Sulfonyl Chlorides concept. You can view video lessons to learn Leaving Group Conversions - Sulfonyl Chlorides. Or if you need more Leaving Group Conversions - Sulfonyl Chlorides practice, you can also practice Leaving Group Conversions - Sulfonyl Chlorides practice problems.
How long does this problem take to solve?
Our expert Organic tutor, Katie took 2 minutes and 37 seconds to solve this problem. You can follow their steps in the video explanation above.
What professor is this problem relevant for?
Based on our data, we think this problem is relevant for Professor Howitz's class at UCI.