May I ask if the reagents and conditions used are listed in this following order: " H2O, H2SO4, 100 degrees, 3h" Will elimination of alcohol occur to give a major product for a compound, or elimination of alcohol does not occur since H2O is in excess? Thank you.
Hi, I have a quick question. In the last reaction you went over (ether formation), how do you control which alcohol is protonated? When introduced to sulfuric acid, can't both the alcohols get protonated at once?
Sir please Answer me the following two questions. 1. Although Nitrogen is more electronegative than carbon ,the direction of the dipole moment is towards the ring? 2. what happens when methylcyclopropene is heated with HBr?
what if we broke the bond between C2 and C3? what will be the expected structure? not sure if you"ll see this comment, but if do your quick response will be appreciated!
You can also compare On the basis of which product have more alpha -H. The compound which have more alpha - H (should see the hydrogens of the carbon next to the doubly bonded carbon) would be the major product
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May I ask if the reagents and conditions used are listed in this following order:
" H2O, H2SO4, 100 degrees, 3h"
Will elimination of alcohol occur to give a major product for a compound, or elimination of alcohol does not occur since H2O is in excess?
Thank you.
im currently studying organic chemistry and its bloody difficult
Thank you once again.
Who thinks we have to go to his account page and just like all his videos😁.
Nice video
Hi, I have a quick question. In the last reaction you went over (ether formation), how do you control which alcohol is protonated? When introduced to sulfuric acid, can't both the alcohols get protonated at once?
Doesn't Matter bcoz we get the same product
@@edgedoff2623 but it doesn't matter because the product is symmetrical. what if the chain has anything attached to it on 3,4,5 positions
I love your work trust me I want to be like you what can I do
Hi! I have a question
at 11:04, can the ring open with carbon 2? or is there a reason for the carbon 6 to open the ring?
do any minor products occur without the 1,2-shift? or is that move so stabilizing that there virtually is none (but even miniscule?)
What we be balanced chemical equation of dehydration reaction of alcohol
At the start of the video, you said the reaction would go through E1, but you didn't explain why :(. Why is it E1 and not E2?
cant you add H3O+ in solvent to give OH the extra H?
Sir please Answer me the following two questions.
1. Although Nitrogen is more electronegative than carbon ,the direction of the dipole moment is towards the ring?
2. what happens when methylcyclopropene is heated with HBr?
@Mani Kantan Thanks, but now I've got the answer.
Happy to meet you all
what if we broke the bond between C2 and C3? what will be the expected structure? not sure if you"ll see this comment, but if do your quick response will be appreciated!
What will happen when 2-methylcyclohexanol is reacted with sulfuric acid at 180 °C??
bro u have already made 2 videos on this topic already
Bro u have already used "already"
More examples are always good in my opinion
thank you so much for this
a major product is just the product that is most abundant, usually the most substituted double bond in these reactions
Have you got the answer? Hahaa if you wanna me to explain, feel free to dm me on my instagram @halalcompliance_
You can also compare On the basis of which product have more alpha -H. The compound which have more alpha - H (should see the hydrogens of the carbon next to the doubly bonded carbon) would be the major product
this video is my question
amazing thank you!
at 11:00 can the bond between carbon 2 and 3 break?
How do you know if it’s going to go e1 or e2?
Can we use setzeff rule to determine stability
Yep but it helps only in case of 2⁰ and 3⁰ alcohols as they follow E¹ path but be careful when it comes to 1⁰ Alcohols which follows E² mechanism!
@@shobanajohn9743 thanks
@@shobanajohn9743 So, do ALL secondary alcohols ONLY go through E1, or can they go through E2 sometimes as well?
amazing man, very helpful, but please, for the love of god, producT
Thanks😊
TLDR; alcohol = ether + water in the presence of H2SO4.
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What about with Al2O3 mechanism it follows E2mechanism?
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