Drawing Mechanisms For Acid-Catalyzed Hydration and Hydrohalogenation Reactions of Alkenes
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In this video we'll cover how to draw the mechanisms for acid-catalyzed hydration reactions and hydrohalogenation. We'll also cover how to quickly spot if a rearrangement will occur and better understand Markovnikov's rule.
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0:00 Acid-Catalyzed Hydration Mechanism
1:51 Identifying Nucleophiles and Electrophiles
13:40 Hydrohalogenation Mechanism
18:17 Rearrangements: Methyl Shift
Пікірлер: 7
For the first question would the final product be on a chiral center leading to enantiomers?
There’s was a bonus question on my exam about this, and I missed one silly mistake on a 10 point acid base equation……😔 How do you get over silly mistakes on the test?
and this is lvl 1 lol AHHHH I'm scared my test is tmr
I just stumbled on your channel looking for Ochem help. I love the format of this video! Makes it more interesting/engaging to follow :)
For the first question, why wouldn't you rearrange the carbocation if you can make it a tertiary instead of secondary?
@michaelkelley3430
8 ай бұрын
A carbocation can only move to adjacent carbons. On its left it had a primary, and on its right it had a secondary which is not greater than the secondary it's on so it stays.
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