Zaitsev’s Rule for elimination reactions

[@motherofkitten]

As a Turkish highschool student, I couldn't find any video like yours for me to understand clearly. Thank you, sir.

[@Chemistryuniversity]

You are welcome!

[@weshendrikx9754]

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[@Chemistryuniversity]

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[@freecoursite1942]

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[@JoDigital_Minds]

Very helpful. I didn't even go through the video; just looked at the Zaitsev's rule and got everything

[@Chemistryuniversity]

Glad it was helpful.

[@johnathann.77]

Thank you so much man I looked 1.5 hours for this

[@Chemistryuniversity]

Glad you found it. I have videos for most of the reactions in undergrad organic chemistry, so others may also be helpful.

[@cholkymilkmirage4984]

so zaitsev major goes after the one with the lowest H's and forms the double bond to stabalize the molecule after the leaving group leaves. The strong base deprotonates the H and the h leaves its electrons behind where the double bond is formed and stabalizing the molecule.

[@aiman_a]

thank you for this video! it was really helpful and totally cleared up my confusion

[@Chemistryuniversity]

You’re welcome

[@Everyday1209-x3u]

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[@Chemistryuniversity]

I am glad you like it.

[@WANAIMANHAKEMIBINDARMAFIKRIUPM]

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[@anjalishah2845]

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[@Chemistryuniversity]

I am glad you like it.

[@anastasiakarpova651]

Thanks you. Perfect explanation!

[@Chemistryuniversity]

You’re welcome.

[@vaishnav4271]

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[@Chemistryuniversity]

You’re welcome

[@freecoursite1942]

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[@alimuhtasham4045]

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[@freecoursite1942]

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