Very important examples from Birch reduction for csir-net exam

[@SumanSharma-cn6om]

There is no words to say thanks
Such a great job

[@4sacademy487]

Ques. 2 me doble bond dusri trf nhi aatega product me pls reply fast

[@pinkimiri2315]

Sir last question me ethanol use kiye to aromatic ring ka v reduction hoga n

[@rebatighosh8283]

Thank you 👍

[@phanindrakumar3221]

Pls do some special questions like the way u always do and boostup our confidence 😊

[@chemistry1683]

What will happen if both EWG and EDG present are present in birch reduction

[@Chemistrylover]

Fate is determined by ewg

[@ranjeetasingh4247]

Sir organic part ko strong kaise bnaye aapke kaise Itna acha explain kr lete hai

[@kashiramgawas8817]

Thank you sir...
Please exsplain in details

[@snehansumohapatra8930]

Very good job bro..u r doing better job.

[@ishwardewagan1778]

Bro can you explain me in then reduction of enone in the presence of metal with liq.ammonia +NH4CL give the saturated ketone ..so why further ketone not reduce into alcohol .and if NH4CL distroy the reduction environment but HOw?

[@Chemistrylover]

It's a radical reaction, and you need conjugation to stabilize a radical, so after the reduction of double bond, the carbonyl group becomes isolated and thus radical can't form, so no further reaction occurs.

[@ishwardewagan1778]

@@Chemistrylover thanku so much 😍

[@pruthvirajnayi5493]

Problem is from jie jack li??

[@Chemistrylover]

Carruthers

[@technicaljmd1504]

Sir upni ki teaching dan???

[@Chemistrylover]

For previous video on Birch reduction : ua-cam.com/video/Cz-pZOgeiDQ/v-deo.html
For mechanism of Birch reduction of conjugated alkene: ua-cam.com/video/Tq9ldXuUE7Q/v-deo.html

[@phanindrakumar3221]

Sir we r waiting for ur vedios

[@PRIYASINGH-hy5ut]

Sir..these examples are from which book?

[@Chemistrylover]

Carruthers

[@adilakshmib6792]

Very informative and good

[@bhagyashripimparkar474]

Looking good bhai

[@Chemistrylover]

Thanks didi

[@amitkumar-zm1qy]

Why are you not writing o, m hydrogenated methoxy cyclohaxane, when Li, liq NH3, EtOH is used?
Instead you write alpha, beta unsaturated carbonyl.

[@Chemistrylover]

I wrote both, I think, can u please mention the time, u talking about?

[@amitkumar-zm1qy]

Product formed at time 4:08 I.e alpha beta unsaturated carbonyl instead of usual case in which OMe lies on double bond

[@Chemistrylover]

Ok, of course the OMe will be there after the reduction step, but I wrote the final product, i.e, after hydrolysis with NH4Cl given in the 2nd step.
Ok?

[@amitkumar-zm1qy]

Thank you very much bhai. You are acting like a filler in my preparation for chemistry.
One again thank you very much.

[@Chemistrylover]

Welcome

[@as-bw6sr]

Ty sir

[@goddusivaji8093]

Thank you sir

[@lakshmibaichemistry8110]

Thank uu sir

[@bhagyashripimparkar474]

Now plz focuss only on org

[@4sacademy487]

Sorry ques 3 me