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Halogenation of Alkenes | Mechanism | Stereochemistry | Examples

  Рет қаралды 3,106

Organic Chemistry with Victor

Organic Chemistry with Victor

Күн бұрын

Пікірлер: 14
@just_josh_scoups_of_icecream
@just_josh_scoups_of_icecream 3 ай бұрын
Can't believe an explanation this good has so low recognition, this is the probably the only video which explained stereochemistry so well Thank u so much i was initially so confused but now its all good thanks to ur amazing explanation
@VictortheOrganicChemistryTutor
@VictortheOrganicChemistryTutor 3 ай бұрын
Glad it was helpful! My channel is fairly new, so hopefully, more students will find it in the future.
@user-ye1so7rv8j
@user-ye1so7rv8j 2 ай бұрын
the video deserve more views!
@VictortheOrganicChemistryTutor
@VictortheOrganicChemistryTutor 2 ай бұрын
Tell this to KZfaq algorithm 😂 I do appreciate your support though. I started seriously posting last September but my channel only started to pick up some pace in the spring, so just give it a bit time and I think more students will see these videos.
@peybak
@peybak 10 ай бұрын
@1:14 Showing the electrons move like that was top notch!
@lidyacorrea8860
@lidyacorrea8860 27 күн бұрын
organic chemistry is a mandatory course for my major, and i underestimated it the entire semester!! the exam is tomorrow and you saved my semester, thank you so much!!
@VictortheOrganicChemistryTutor
@VictortheOrganicChemistryTutor 26 күн бұрын
Yeah, organic chemistry is definitely a daily commitment. I’m glad my video helped you.
@Nick-jw1gr
@Nick-jw1gr 3 ай бұрын
Love your videos! You always give amazing tips and give clear explanations
@VictortheOrganicChemistryTutor
@VictortheOrganicChemistryTutor 3 ай бұрын
Glad you like them! I try doing my best with the explanations 😊
@karola9236
@karola9236 5 ай бұрын
Thanks
@ANURAGIITG202
@ANURAGIITG202 5 ай бұрын
Which app do you use for notes taking ?
@melazaskhia9512
@melazaskhia9512 10 ай бұрын
help me to answer this question 2-heptanone+iodine, with catalysm NaOH plisss
@rockubabe
@rockubabe 8 ай бұрын
In your first example at 5:15, isn't the bond between the C and BR SP3 hybridization? I thought the bond would be flat without coming forward or backward. Also, I is more electronegative than Cl, doesn't that mean I should be partial negative? Not partial positive?
@VictortheOrganicChemistryTutor
@VictortheOrganicChemistryTutor 8 ай бұрын
Bond cannot have any hybridization. It’s the carbon that’s sp3 hybridized. And precisely because of that it has a tetrahedral geometry. No, iodine is not more electronegative than chlorine. Look at your periodic table.
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