21 Replies
@Dexter
Note for OP
+solved @user1 @user2... to close the thread when your doubt is solved. Mention the users who helped you solve the doubt. This will be added to their stats.Very good lg tosylate
What is a tosylate group?
What is a tosylate group?
So will it act like alkyl halide in presence of Nucleophile
@iTeachChem @myst1cboomer
no basically it will just leave easily
no detatchment issues
What will happen in this que? This is dehydrohalogenation (E2 mech) @myst1cboomer
this does not look like dehydrohalogenation
lemme check this
1. strong base
2. heat
What do you think is best here?
James Ashenhurst
Master Organic Chemistry
Wrapup: The Key Factors For Determining SN1/SN2/E1/E2
How do you tell if a reaction goes through SN1, SN2, E1 or E2? Follow these steps to identify the most likely reaction mechanism, with quizzes
yeah elimintation is the way
It is though🙂‍↕️
oTs and H nikal raha hai na e2 hoga
Okyy thnks
The product will be Hoffmann @Real potato as no hydrogen is present in anti position
Can you elaborate this? Does this have to do with the reaction mechanism in anyway? I am oc noob :D
E2 mech requires anti periplanar arrangement of lg and h atom
https://www.masterorganicchemistry.com/2015/04/16/elimination-reactions-of-alcohols/
Does it have something to do with trans Alkenes more stable? Or something in the original mechanism itself that favours the anti H thingy
James Ashenhurst
Master Organic Chemistry
Elimination Reactions of Alcohols
All about elimination of alcohols using strong acids with non-nucleophilic counterions, such as H2SO4, H3PO4, and TsOH. Mostly E1, but E2 for primary cases.
Ah okay!
Ty Ty
Yes i know that
+solved @Ghostty
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