Very helpful sir...all rexns were clearly taught nd explained...much impressed by you....now it will be easy to learn these rexns..thankyou so much sir..#respect for you..😊😊🙏🙏
An easier way to explain the Markovnicov product. Because a secondary carbocation is more stable than a primary carbocation, the hydrogen is more favorably removed by a nucleophile from the secondary carbon on the left to create the more stable carbocation.
he's the first person to explain reactions that actually makes sense!!! THANK YOU!!
Thanks ,i learned more than what i expected.
I'm glad you learned some things. Welcome to the channel!
Thanks alot ,Cant wait to watch all your tutorials
thanku so much sir. i was really having difficulty to revise these reactions and now im able to recognise and write them down.
thanku #respect
As a person who has master degree in organic chemistry, I found him one of the best teachers.
ua-cam.com/video/jqULg4szkus/v-deo.html
Very helpful sir...all rexns were clearly taught nd explained...much impressed by you....now it will be easy to learn these rexns..thankyou so much sir..#respect for you..😊😊🙏🙏
very helpful! thanks,sir.
👍
this tutorial is really the best,thanks sir.
Thankyou, Sir.May God bless you.
You're welcome!
much clear content..thenks much Sir
Thank you for ur easy explaining 🤍.
Thanks you sir your vedio is very helpful.
An easier way to explain the Markovnicov product. Because a secondary carbocation is more stable than a primary carbocation, the hydrogen is more favorably removed by a nucleophile from the secondary carbon on the left to create the more stable carbocation.
very helpful 👍
very helpful thank you sir.
very nice sir it really helped me
Someone give this man my most sincere thanks, he is truly making a difference!
simple understand to reaction, so thank you sir.
thank you so much professor, tomorrow is my exam you just helped me get good grades..
Wonderful from Nigeria
Very Clear sir..From Kisii,Kenya.
Wow! You have done an AMAZING job! thank you :)
Very helpful thanks sir
Also- For the primary alcohol (1 degree alcohol), the aldehydes can be further oxidized to carboxylic acids. ☺️
ua-cam.com/video/jqULg4szkus/v-deo.html
But under strong oxidising agent
excellent video
May Allah bless you
A great teacher
Thank you, Nice explanation!
thank you sir, this is very helpful
Madala ndinu Dada
Thumbs up
thank you so much sir, i finally understand this
The great from Ethiopia
thanks for watching
Thank you soo much sir
Thank you so much this really clarified alot for me
bundle of thanks for u and please upload more
Wonderful!!!
Thank you so much.. Very clear😍
i hope you are my professor in chemistry...thanks
thankue Sir
Nice video
Thank you so much
Finally it makes sense to me😭
Thank you soo much sir❤️🙏✨
Thank u sir
I wish to you long life full of sciences
Nice
I hope you are okay sir:(
Thanks sir
thankyou so much sir!! i understand so much better!!! Before that i was just a lost sheep in ochem ahhaa
Very good!
Thank you very much 💕
Nice Sweater Vest #Classy
Best of the best
thank u very much
Respected sir , can u explain me that why alohol do not react with NaOH or KOH?
thank you sooo much sir, i really do understand :)
Why no electron pushing???
Proficiency is recognizable in you
isnt the dehydration done with conc phosphoric acid?? help
oh it can be both nvm
nice
thank you so much ^_^
❤❤❤❤❤
I appreciate thank you so much
thank.you.so.much.
Noice.
maybe it could help me