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 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..😊😊🙏🙏
he's the first person to explain reactions that actually makes sense!!! THANK YOU!!
thanku so much sir. i was really having difficulty to revise these reactions and now im able to recognise and write them down.
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Thanks ,i learned more than what i expected.
I'm glad you learned some things. Welcome to the channel!
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ua-cam.com/video/jqULg4szkus/v-deo.html
Thankyou, Sir.May God bless you.
You're welcome!
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! 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
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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..😊😊🙏🙏
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Wonderful from Nigeria
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simple understand to reaction, so thank you sir.
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Very Clear sir..From Kisii,Kenya.
May Allah bless you
The great from Ethiopia
thanks for watching
Madala ndinu Dada
Thumbs up
Thank you, Nice explanation!
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Respected sir , can u explain me that why alohol do not react with NaOH or KOH?
I hope you are okay sir:(
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isnt the dehydration done with conc phosphoric acid?? help
oh it can be both nvm
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Best of the best
Why no electron pushing???
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maybe it could help me