8.7 Expoxidation, Anti-Dihydroxylation, and Syn-Dihydroxylation of Alkenes | Organic Chemistry

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Just watched all of chapter 8 from you and it was amazing, thank you so much Chad!

[@ChadsPrep]

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thank you!!! final exam tmr, and i learned more from you than my professor!!!!!!!

[@ChadsPrep]

Glad the channel has been helping you - Hope you do well on your final!

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This was amazing, I feel like I've learned a lot, thank you so much!!!

[@ChadsPrep]

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[@Riya-zo8nq]

for anti, u said its something to talk about for semester 2 but can u explain it why you attacked the top bond rather than the bottom, is there a preference when there are the same amount of subs?

[@onespeedbjj3846]

Why would the double bond in cyclohexene do a nucleophilic attach on Oxygen isn’t oxygen partially negative?

[@BigAbeFishing]

Thank you sir, that was incredibly helpful and informative!!

[@ChadsPrep]

You're welcome, Abraam - Glad it helped you!

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thank you very much hi from Turkey

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[@universitydocs]

I've been told cyclohexanes do not follow the interpretations of 2d drawing so I notice a contradiction from what I learned, in the product of the syn addition. I genuinely am curious can I continue to rely on the 3d model of cyclohexane to tell me whether the product in the syn addition would be meso? I was thinking since the OH's are on adjacent carbons in the 3d conformation there does not seem to be a plane of symmetry unless I'm interpreting it wrong.

[@thayhuongchuyenhoalekhietq6803]

Great job!

[@ChadsPrep]

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You're welcome, from U.S.A.

[@abdoulazizdabo9064]

Thank you ❤

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[@furfoxsake1175]

I'm one of the lucky students who has to know the mechanism for syn dihydroxylation

[@ChadsPrep]

Lucky indeed!

[@nealkumar3257]

hi at 5.55 should the wedge bond between c and o where the h2o is attacking be removed

[@nealkumar3257]

like shouldn't there be arrows going from the c-o bond to the oxygen

[@thebluebeyond2329]

Awesome

[@ChadsPrep]

Thanks!

[@N8_DoubleYou]

CPM=0.93 ⚠

[@ChadsPrep]

Alright N8 DoubleYou, why the CPM comments?