Hey Francesca! Unfortunately I do not have much advice for that. If you really can't continue your synthesis but know that the next step that is a Reduction/Oxidation/Elimination/Substitution/Dehydration/Aldol reaction then you can try and write one of those to atleast try and get partial credit. The important thing is showing what you know and getting to the point in the synthesis where you can continue. I'm not sure what the ACS exam and it's format though. Sorry =/
Hey. I'm reviewing for the ACS exam and I wanted to know if there is a general technique that you use to predict the products or reactants for synthesis reactions that you may not remember on test day.
+vishua TYTY :] Go kick some alkene butt now. Btw these other peeps are really really good too! ua-cam.com/video/1QkGxQCI1es/v-deo.html Although I still say I'm the best hehehe :D
sir i want to ask that i had read in many books that in acid catalyed reaction the product is a mixture of sec and tert alcohol..!!...acc to me it should me either sec or tert alcohol not mixture?????
The moment they go into the water, they act as a strong acid releasing 1 Hydrogen which then bonds with an H2O molecule to form H3O+. Sorry, about the confusion haha
Wow! After 1,000 UA-cam videos and still not understanding, you make it seem so much easier within 5 minutes. Thank yooou!
+Adriane Kelley :D Your welcome Adriane! It really is just that simple ;) glad the vid could help!
Please make more videos! You have such an incredible gift! I now understand certain concepts I would not have understood otherwise.
Haha I love the humor you add into your videos, it makes your videos fun to watch!
Lol yay! I'm glad there are people who get my humor haha, thanks for watching and keep up your hard work!
Thanks for the video, it makes a lot of sense. Do you have a video on acid-catalyzed dehydration?
Wow, thanks E Bebo! Keep going at it with Orgo, wish you the best of luck!
Thank you🥺🥺. This stuff almost frustrated me, you made it easier 😤
Glad to hear that I could help Xaiver!! Good luck! 💪🏼
You, sir, are a life saver man!
I'm your newest subscriber!!!
Woooo! I'm just glad I could help Harrison Gachanjah! ;)
Kudos I like your content including the English language ♥️
Hey Francesca! Unfortunately I do not have much advice for that. If you really can't continue your synthesis but know that the next step that is a Reduction/Oxidation/Elimination/Substitution/Dehydration/Aldol reaction then you can try and write one of those to atleast try and get partial credit. The important thing is showing what you know and getting to the point in the synthesis where you can continue. I'm not sure what the ACS exam and it's format though. Sorry =/
Thanks Brandon! I appreciate the positive feedback. :] Hope Orgo can actually be a little more fun now.
Love your videos, thank you!
hey frank ur way of teachin is coooll i cant find the videos dat teach da basics... cn u see to it
Thanks so much! I really learned soooo much from your video! love your teaching style!
You make this stuff easy and digestible. ;) THANKS!
Please make more vids! They are so great and helpful! :]
Haha yay! Thanks Grace, glad to hear it was helpful for you. I'll try to keep teaching the same way than haha.
Hey. I'm reviewing for the ACS exam and I wanted to know if there is a general technique that you use to predict the products or reactants for synthesis reactions that you may not remember on test day.
Nice discussion, thanks bruh :]]]
good one.. pls go through hydrobaration wiki page also...
anion attacking boron is hydroperoxide(-OOH) not hydroxide (-OH)
Nice video
oh my god ur the best!!!!!!!!!!!!!!!!!
+vishua TYTY :] Go kick some alkene butt now. Btw these other peeps are really really good too! ua-cam.com/video/1QkGxQCI1es/v-deo.html Although I still say I'm the best hehehe :D
SO HELPFUL
I'm glad to hear! Hope I made Organic Chem a bit more fun ;)
ha yeah man its great when ya get it. Got my alkene/alkyne reaction/mechanism test tomorrow :O
Thank you!
you are amazing thanks !!
what I don't get is on the protonation step water has two lone pairs yet only one pair is used do we ignore the remaining pair
They then just remain in solution as either Cl- or HSO4-.
Why do you put the H in the between the two H's and the OH in between the CH3 and H?
thanks for the vid
sir i want to ask that i had read in many books that in acid catalyed reaction the product is a mixture of sec and tert alcohol..!!...acc to me it should me either sec or tert alcohol not mixture?????
The moment they go into the water, they act as a strong acid releasing 1 Hydrogen which then bonds with an H2O molecule to form H3O+. Sorry, about the confusion haha
How is this done in line structure..
Doesn't it form two products?Racemization?
Anyone watching in 2020? Nah, I'm just playing
If you leave water attached to the molecule, you're gonna have a bad time
Yes! A very bad time indeed... ;]
Great video, but the example is too simple
you don't go into depth with arrows and what not. you really should as it explains why you're adding the Oh where you're adding it.
That's all in part 2 ;) the mechanism video.
i didnt hit the pause button.. u dont own meeee!!!!
Marry me!