Sir conversions karna bekar nahi tha , bahut sikhne ko mila , syllabus cover hone ke bad , agar apke pas samay hai to conversions ka 2-3 videos aur bana dijiye. Thank you sir.
16:53 for those who are thinking why we are using bromination ,not using chlorination again ; because chlorine will attack on Ortho position note on para position because of a small size
21:20 Aise kar sakte hay kya First chlorination Then sulphonation ( para me SO3H lgega) Then bromination ( Cl ke ortho me Br lgega). Then desulphonation ( SO3H hat jyega) Then Mg + dry ether Then di grignard reagent se O2 and hydrolysis krke final product
38:25 sir carbonic acid kuch extent me to banta hoga aur le chatelier principle se to co2 aur h20 me convert hone par equilibrium forward shift hona chahiye
Benzene to hydroquinone can also be prepared by : Chlorination of benzene gives chlorobenzene . Further chlorination of chlorobenzene gives major product as p-chloro chlorobenzene . Applying Dow's Process to p-chloro chlorobenzene , hydroquinone can be made .(benzyne mechanism) SIR PLEASE CHECK THIS METHOD!!!🙏🙏
Sir conversions karna bekar nahi tha , bahut sikhne ko mila , syllabus cover hone ke bad , agar apke pas samay hai to conversions ka 2-3 videos aur bana dijiye. Thank you sir.
16:53 for those who are thinking why we are using bromination ,not using chlorination again ; because chlorine will attack on Ortho position note on para position because of a small size
But fir 3 question me consecutively cl2 alcl3 kyu use nahi Kiya?? please tell
23:00
Mononitration-->bromination-->reduction of nitro to Nh2 -->diazotisation-->sandmeyer reaction
Sir in 21:56 we can do sulphonation rather than doing nitration as we can remove SO3H in just one step.
IPSO attack will happen and HSO3 will be removed by chlorine itself
21:20
Aise kar sakte hay kya
First chlorination
Then sulphonation ( para me SO3H lgega)
Then bromination ( Cl ke ortho me Br lgega).
Then desulphonation ( SO3H hat jyega)
Then Mg + dry ether
Then di grignard reagent se O2 and hydrolysis krke final product
6th 1) sn hcl 2) kno2 + hcl 3 ) heat + c2h5cl alcl3 4 hcn + cucn 4) h3o + heat.
Actually nh2 is an activating group, it won't show friedel craft alkylation, try converting nh2 to nhcoch3 and then proceed to do the alkylation
These interconversion questions were really helpful sir! They were all like summaries of orm 2, some reduction, and this chapter
to form hydroquinone and catechol we can simply do 1) phenol formation using v2o5 ,,,,, and then 2) Elbs rxn
5 th 1) cl2+alcl3 2) mg +ether 3) co2 (orm 1) 4 c2h5cl alcl3
Very nice solution
Bro iit mili terko?
Excellent lecture sir
54:46 less hindered alcohol
38:25 sir carbonic acid kuch extent me to banta hoga aur le chatelier principle se to co2 aur h20 me convert hone par equilibrium forward shift hona chahiye
obviously
Sir 27:40 par apka soln me zn amalgum in presence of hcl no2 ko nh2 me convert kar dega diazotization ki jarurat hi nhi thi
Sir 21:27 me di grignard reagent nahi banta hai benzyne mechanism me do benzene ring se jud jayenge
Benzene to hydroquinone can also be prepared by :
Chlorination of benzene gives chlorobenzene . Further chlorination of chlorobenzene gives major product as p-chloro chlorobenzene . Applying Dow's Process to p-chloro chlorobenzene , hydroquinone can be made .(benzyne mechanism)
SIR PLEASE CHECK THIS METHOD!!!🙏🙏
2 video in day thnks sor
For 5th interconversion, can we do this?:
[Benzene] > V205 (300°C) > Sulphonation > rex with XMg-COOH > Zn dust+∆ > CH3-CH2-Cl + AlCl3
7:23 zenith reaction
13:00 acetanillide qn came in jee m 2021
Thanks sir
It was a good revision of orm2, and the first 4 vids of this chapter
Sir P isomer me two times chlorination krwa kr dow's method se bn jata
Yes maine same yahi kiya
2 video in a day 😃😃😃😃
Sir first Fenton's and then elps persulpgare reactions
Thanks
Tq sir
47:15 sir yaha SN2’ reaction nahi hoga?
The mechanism followed is SN2 only.
Agar hum do molecule V2O5, 300°C pe le tooo hydroquinone banega kya aur nahi to fr q?
56:40
sir, phenoxide me steric hindrance ortho position pr km kese ho skta h compared to para ? can u pls tell ?
FOR CATECHOL WHY NOT JUST NITRATE TWICE THEN REDUCE THEN DIAZO?
The NH2 would be in ortho position of the other NH2, in which case it wouldn't undergo diazotization.
thanks sir
nice name.....reminds me of mom