You taught me about chemical bonds, Acids, formal charges etc while studying in my home country. Now I am a 2nd Year Pharmacy student, still here. Thanks a lot. COOL!
Thank you for everything!! I got sick for a couple days and it was enough to make me fall behind during the hardest part of the course. I've been working every day to catch up and it's only possible because of your videos. You're an excellent teacher and thank you for sharing your videos for free. I might end up grabbing your premium course for the rest of the semester... I just wish I had started with your premium course from the beginning of the semester!!
I’m doing my pre medical program and have come across your videos recently. Life changing videos u’ve got. Let’s get through this final stage together!!!!🙌
Oh, Chad, you’re the king of the chem, You make alkanes and esters feel like friends. With your tricks and tips, I’m feeling breezy, Oh, Chad, you make organic chem so easy!
Awesome Alyssa and I'm glad you're enjoying the Ultimate Bundle! It is truly amazing that technology makes it possible to deliver so much value for such a low price. I can't imagine what learning in a pandemic would have been like even 10 years ago. Happy Studying!
Nice video Please also mention the effect of electron withdrawing grp such as phenyl carbonyl group that increase the rate of reaction As transition state becomes more stable
Sir we commonly say that a weak acid has a strong conjugate base .....as well as nucleophilic strength of a nucleophile is also decided by how much weak acid is using in the reaction ...... When we use KOH in the presence of water, major product is due to substitution reaction ......while KOH in the presence of Alcohol reaction shifts towards elimination reaction .....it means in water a good nucleophile is produced but in alcohol a good base is produced.....in both cases alcohol is slightly acidic than water ....is it the peculiar behavior or my concept about strength of base and nucleophile is wrong? Looking for your guidance thank u
@@ChadsPrep Thanks for answering! In the video you are telling "... And when you just double the volume of solvent, but kept the numbers of moles of these constant, you just cut their volumes in half." But thats wrong, because you don't cut their volumes in half when diluting, but you cut their concentrations in half.
You taught me about chemical bonds, Acids, formal charges etc while studying in my home country. Now I am a 2nd Year Pharmacy student, still here. Thanks a lot. COOL!
Glad to hear it, Wayne - keep up the hard work!
@@ChadsPrep Jacob job medicure sazzzqqm
Chapter 7 has been a nightmare. Your vids help so much. Thank you Chad!
You're welcome
Thank you for everything!! I got sick for a couple days and it was enough to make me fall behind during the hardest part of the course. I've been working every day to catch up and it's only possible because of your videos. You're an excellent teacher and thank you for sharing your videos for free. I might end up grabbing your premium course for the rest of the semester... I just wish I had started with your premium course from the beginning of the semester!!
Glad the channel is helping you out - I hope you are able to recover and get back on track. Happy Studying!
I’m doing my pre medical program and have come across your videos recently. Life changing videos u’ve got.
Let’s get through this final stage together!!!!🙌
Glad you found us - Happy Studying!
"Your teaching is like a strong acid-always breaking things down to make them easier to understand!"
Thanks for saying so!
@@ChadsPrep my pleasure to have teacher like you
@@princeysuryan2561
Oh, Chad, you’re the king of the chem,
You make alkanes and esters feel like friends.
With your tricks and tips, I’m feeling breezy,
Oh, Chad, you make organic chem so easy!
Your poem I hear
It feels like you're near
Your words make me grin
Much laughter for the win!
God bless you. That’s all I can say! You’re my savior!
Glad you found the channel!
thanks man, I know you probably hear it alot but these videos are really helpful and I appreciate you making them.
I'm glad to hear it every time, Will - always good to hear students benefit from the videos. Happy Studying!
One of your best videos I've seen, thanks Chad!
You're welcome and Thank You!
My fave professor! So happy to have found you! I have purchased the premium bundle and it is AMAZING
Awesome Alyssa and I'm glad you're enjoying the Ultimate Bundle! It is truly amazing that technology makes it possible to deliver so much value for such a low price. I can't imagine what learning in a pandemic would have been like even 10 years ago.
Happy Studying!
You’re better than my professor! Really clear demonstration! Thanks
Very welcome
I wish you could be my professor omg! helped me through all my chem classes
Glad you find the videos helpful, Seda - Happy Studying!
Back-side attack lol.
Great video as always Sir. Thank you.
You're welcome
Your an awesome teacher.. just saying.
Thanks DS! Glad you're finding these lessons helpful!
Nice video
Please also mention the effect of electron withdrawing grp such as phenyl carbonyl group that increase the rate of reaction
As transition state becomes more stable
Thank you again, Chad!
Thank you teacher .you are perfect 👌🏻🌸
You're welcome - thank you!
Thanks so much Chad!! Really appreciate it!
You're welcome, Timothy!
I can't thank you enough, this was so much helpful🙏
Glad to hear it!
very good
Thank you
You are amazing Sir!
Thank you kindly!
Thank you greatly. Brilliant.
You're welcome and Thank You!
Sir we commonly say that a weak acid has a strong conjugate base .....as well as nucleophilic strength of a nucleophile is also decided by how much weak acid is using in the reaction ......
When we use KOH in the presence of water, major product is due to substitution reaction ......while KOH in the presence of Alcohol reaction shifts towards elimination reaction .....it means in water a good nucleophile is produced but in alcohol a good base is produced.....in both cases alcohol is slightly acidic than water ....is it the peculiar behavior or my concept about strength of base and nucleophile is wrong?
Looking for your guidance thank u
This was great!
Thanks for saying so!
why isn’t there a SN reaction video?
do you mean SN1?
My medschool tuition should go to you
Glad you find such value in the channel!
i love you chad
Glad the channel is helping!
G.O.A.T.
Thanks Jake and Happy Thanksgiving!
Why did you not put Br or NaBr as a product?
Hey Julia - in which reaction (can you give the time in the video)
At 7:50 you said "cut their volume in half", but you meant "cut their concentration in half"...
I definitely meant volume - if we increase the volume of acetone the solvent it changes the concentration by diluting it
@@ChadsPrep Thanks for answering!
In the video you are telling "... And when you just double the volume of solvent, but kept the numbers of moles of these constant, you just cut their volumes in half."
But thats wrong, because you don't cut their volumes in half when diluting, but you cut their concentrations in half.
Trigonal planar? I think it’s more trigonal bipyramidal
I think since it's a transition state, it is trigonal planar as the molecule is still in the process of switching bonds, per se.
the carbon is approximately sp2 hybridized so its trigonal planar
i love you
Glad the channel is helping you!
i became a pharmacist because of you now . How can i thank you
I think you just did!