Alcohol Dehydration Reaction Mechanism With H2SO4

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Thank you for the video, The trick you show help a lot to distinguish between minor vs major product

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[@NewWesternFront]

do any minor products occur without the 1,2-shift? or is that move so stabilizing that there virtually is none (but even miniscule?)

[@UsherCoolboySWFilms]

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?

[@jaytan2649]

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.

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[@cheema9410]

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?

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[@Msraeli100]

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?

[@akcsamiru]

cant you add H3O+ in solvent to give OH the extra H?

[@mercilessmirage9789]

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?

[@edgedoff2623]

Doesn't Matter bcoz we get the same product

[@phymath8038]

​@@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

[@morindolph8438]

at 11:00 can the bond between carbon 2 and 3 break?

[@danielmwanamonga6880]

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!

[@sanika212]

What we be balanced chemical equation of dehydration reaction of alcohol

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What will happen when 2-methylcyclohexanol is reacted with sulfuric acid at 180 °C??

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Can we use setzeff rule to determine stability

[@shobanajohn9743]

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!

[@madhuswami9836]

@@shobanajohn9743 thanks

[@UsherCoolboySWFilms]

@@shobanajohn9743 So, do ALL secondary alcohols ONLY go through E1, or can they go through E2 sometimes as well?

[@daniellai7601]

How do you know if it’s going to go e1 or e2?

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[@elissawong3964]

a major product is just the product that is most abundant, usually the most substituted double bond in these reactions

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[@shobanajohn9743]

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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[@srinivas3835]

What about with Al2O3 mechanism it follows E2mechanism?

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14:58

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TLDR; alcohol = ether + water in the presence of H2SO4.

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