Organic Chemistry 1 Exam 2 Review

[@TheOrganicChemistryTutor]

Organic Chemistry PDF Worksheets: www.video-tutor.net/orgo-chem.html Full-Length Exams & PDF Worksheets: www.patreon.com/MathScienceTutor/collections Full 3 Hour 44 Minute Video on Patreon: bit.ly/420cTys Download The Exam - 85 Test Questions: bit.ly/3GaWI7V

[@iwishiwasfaster]

how did you know I had an exam today?

[@calebkimmel372]

organic chemistry tutor my beloved i would trust you with my life thank you for your service

[@nick_0]

How did he know I got exam 2 next week 😂 bros timing is impeccable

[@fairyyoongi]

the most difficult for me is the SN1 and SN2 reactions

[@qoaeramv]

Sn1/E1 and sn2/E2 reactions are the hardest combined with alkene alkyne reactions

[@christianborja154]

I agree

[@parakhmody1413]

43:05 to 43:17 Here you say we can infer endothermic or exothermic based on the potential energy diagram, but I dont believe that is correct. The potential energy or free energy may tell us about endergonic or exergonic, but we can't assume that to mean the heat of reaction (positive or negative). Do let me know yoir thoughts.

[@kime394]

It’s like you knew I was studying for this thank you for this video!

[@abdulbariabumahama]

God bless you man it’s like you’ve been sent to help ❤❤🙏

[@thatomofolo452]

Yesss Thank You Mr J ✌️✌️✌️😃

[@jmil0609]

Hell yea I got exam 3 in 3 weeks please get that one out your the man

[@TheWTFcakes]

Isnt the only difference between enantiomers their plane-polarized light?

[@elienassif8676]

Don't enantiomers have the same physical properties other than rotation of polarized light?

[@AryamAman]

@49:20 Sir the rate of SN1 depends on the stability of "First Formed Carbocation" So according to this 1st one has more Alpha H in in its first formed C+, hence 1st has more rate of ren than the 2nd one.... Please review, thànks

[@chrismargolis]

Wait that’s how it works? Wouldn’t the first formed carbocation of the second structure be more stable because it is closer to a large electron donating group?

[@crazedtanki233]

3 degree carbo is more stable than 2 degree, and that itself is enough for it to be faster.....alpha hydrogens would come into play if they both were both 2 degree since the start

[@yasminegermain4765]

God is using you to help me pass this exam wow!

[@martinbobak3009]

He would have to exist in the first order

[@nicoled6477]

Hardest for me is the alkene and alkyne reactions, easily confused

[@lilliankabotolo689]

Thank you so much sir you've really helped me a lot

[@Stuckinthepow]

At 13.:5 isn't that first diol exhibiting symmetry therefore MESO? Just asking. TY

[@Willisflame]

What is an r configuration

[@emilynhaxx]

I struggle the most with reactions.

[@thisisrakia6906]

Hi. Please can you make a video about interplaner spacing and miller indices and family of planes on physics please? I’m having exams next month and I don’t understand the topics 🥺

[@thisisrakia6906]

Please? 🥺

[@martinbobak3009]

​@@thisisrakia6906 heard of Google?

[@thisisrakia6906]

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[@martinbobak3009]

@@thisisrakia6906 ok so you can't use google

[@thisisrakia6906]

@@martinbobak3009 I can use google obviously, but I understand his tutorials more. Don’t you get?

[@vaderxtrooper]

Big fan 😁👍

[@MyeonTokki]

ugh why is this so hard

[@deefdean7223]

Where is the question?

[@thatomofolo452]

Dope 🔥🔥🔥💯🤧

[@ShadowMonarch988]

Good

[@vincentmudimeli4430]

I find strrio chem confusing

[@TheCosmicGuy0111]

Cool!

[@Hearts4Kekee]

HELP‼‼ HOW DO I TEST THIS - (ITS A PLAN AND DESIGN LAB) A student observed that whenever she ate peanuts of brand x, she became thristier than if she ate peanuts of brand y. Hypothesis: Brand X peanuts contain more salt/sodium than Brand y

[@bluccos8884]

🐐

[@yaibolayuel9078]

My problems are stereochemistry and nomenclature of heterocyclic compounds, thanks 🙏