Conformation and Stereochemistry of CYCLOHEXANE [TRICKS and TIPS] | Organic Chemistry

In this video we will learn about different conformations of cyclohexane and their relative stability with the stereochemistry of substituents involved.
#stereochemistry #cyclohexane #conformation #tricks #boat #chair #half
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SAHANUJ PAIK, thank you for your kind words...
You can watch many videos on different important topics... There are total 45 such videos, make sure you SUBSCRIBE the channel to get notification regarding future updates.

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Option 1 will be right because the -OH group present on axial will form hydrogen bonds with oxygen

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A is the answer

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All 'Bout Chemistry option 1
OH at a position and Me at e position

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Which one is least stable !!

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Option 1 is most stable

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Boat, twist boat, half chair- which position is axial and equitorial

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Hello sir ! Please provide one 1 video on R / S naming in Ansa compund and Cyclophane .

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If OH group is present in 1,3 position, then will u explain the stability order among the conformers, 1a,3a. 1a,3e. 1e,3a. and 1e,3e will be?? Plz answer

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Option 1
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How deepa .. 1,4 cis is axial equatorial. Option c is crct

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Opt 1 which I mentioned is the answer for the question which is lastly asked in the vedio

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@@deepab6217 methyl or hydroxy which is bulky group ya

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Opt 1 is crct ya give expalination

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Bulkiness is not the deciding factor for the Stable confirmation of that compound.intramolecular hydrogen bond formation between o and H of OH makes it more stable.hence I chose opt 1

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statistical and quantum chemistry

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Is it option one sir????
Please reply

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Ans is 1

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Sir in case of 1,2 disubstituted cyclohexane .
ee will be stable in case of 1,2 dimethycyclohexane and if we have D instead CH3 then ee or ae will stable

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e e

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Option 1

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Option 1 is correct,
Check out this video for solved answer of this question, th-cam.com/video/4ZZJ4JWujso/w-d-xo.html

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Which book you prefer for organic chemistry and physical

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1st one

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Option A

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Its 1 most stable one

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Option 3

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Praveena Gunna,
Check out this video for solved answer of this question, th-cam.com/video/4ZZJ4JWujso/w-d-xo.html

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Btw, well tried... 👍

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Does not explain the stereochemistry (optical activity) of cyclohexane. Misleading title

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Both A& C be the answer

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Is ans for last one is 1 st

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B

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1st is correct