Regioselectivity, stereoselectivity, and stereospecificity

[@ceciliadelattre6603]

Thank you so much for that awesome video!! It had been for 2 years I had not understood the difference btw stereospecificity and stereoselectivity and now I have and thaaannkk yoooouu sooo muuch!!!!

[@shubhkapoor4057]

Most concise and efficient explanation out there! Great video

[@anaghatal3292]

Both regioselective and sterioselective have a major product and a minor one, whats the difference between them?

[@origamigek]

Regioselective makes for a very different connectivity between bonds, essentially a very different molecule. Stereo makes the same molecule almost, with the same connectivity but different shape.

[@anaghatal3292]

Okay, got it. Thank you

[@samratdutta4213]

Thank you for your excellent explanation ❤️

[@rekhapargaie3823]

Best explanation ever.

[@jyothirmaipujari1256]

Thank you sir

[@musicmeister1313]

describe what the stereochemistry is at the carbons tho cuz some of us can't tell just by looking

[@richardaudet1161]

Hello. Very clear explanation. However, nagging question remains: How would you go about changing an achiral molecule into a selected stereoisomer? Can stereoisomers be separated (given they have same solubility, melting/boiling point, etc)?

[@mounikab8735]

Genarally in the stereoisomers ,enantiomers and daistereomersand optical isomers are there.in this diastereomers have different properties so easily separatable.but,for enantimers there is one only difference inthe properties is rotation of direction of light.for these type of compounds,1 1)biological resolution,by using specific microbes ,which digest specific stereoisomer. 2)resolution through diastereomers. And etc.by using these techniques they will be separated.

[@dhruvmittal5156]

What a great video keep it up

[@svseshagiri6665]

Sir can you say how to find the major and minor product please

[@PauloJAdams]

3:24 doesn’t it have to be antiperiplanar to undergo e2

[@sandrozernicki]

Yep, but you need to take into account the Sigma bond between Alpha and Beta carbons.... Sigma bonds rotate, and when the rotation gives the possibility of the antiperiplanar situation to occur... it will occur and due to the distribution of the atoms, we will have the Z product. (sorry for my English)

[@ijazkhan416]

Hellow sir nice explanation👍👍

[@reginecuevas4540]

can you show us the mechanism of stereospecificity?

[@aryan_kode]

Best explained

[@rassimsimou1594]

Good

[@abdollah5276]

Thank youv❤

[@TheTaurusGaming]

great video's!

[@MR-bb9gu]

Please tell the name of comoounds in stereoselective reaction eg

[@sasukeuchiha1320]

Phenyl propanol

[@riyaraj7091]

Thanku

[@betul4922]

I just wanna ask somethin, we said that e1 rxn should be from anti planar?? But in 4:10 it is from syn planar??

[@gungun2063]

Btw,it is E2 reaction and it is always anti eliminating

[@aryanpandey1084]

thanks a lot

[@SLSTCHEMISTRY-t2t]

Thanks

[@PakChemist]

You are good but I can teach this topic more clearly

[@teacher850]

great....

[@RowardRowapore]

Explain as if you are teaching a student who is new on this stuff.

[@umakantgaurav760]

speak a bit slow...Speaking so fast does'nt makes any sense.Eveyone is not so good in english.

[@prakashkunwar1085]

haha streetshitters don't know english

[@babitaagarwal961]

its for foreign students

[@user-wk2gp3tu8h]

Thank you sir