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04:36
@Safdar hi
 
2 hours later…
06:29
@YusufHasan hi ! Are you here ?
07:03
@Safdar hi
@Safdar @satan29 @sai-kartik is anyone among you around ? I have to ask something
you can ask you know..
@Safdar actually I had confusion in Gibbs free energy. And I want a discussion
then give me 10 mins.. ill be there then..
Ok ping me when you are back
07:33
@Safdar are you done now ?
@ronakjain what is your doubt?
@Safdar if you don't mind can you look at my conversation with John Rannie sir. I had described that in room for me and John Rannie
@Safdar look at the total conversation of today....
@ronakjain What is it that you want to prove? del(G) = del(Go) +RTln(Q)?
@Safdar did you read the complete discussion. That's not too long. The proof of this is not problem.
@ronakjain I couldn't understand properly. Or gibbs free energy at a given time t?
07:40
Ok let me explain....
not considering kinetics ofcourse.
Firstly tell me thet is it true that Gibbs function of any species is G = G° + RTln(C). Right ?
@Safdar right ?
@ronakjain Here Go is? standard free energy of what?
For any species. G° is its standard Gibbs function. I will use subscript for different species.
Ok so far ?
@Safdar tell me is it right or not ?
@ronakjain One min.. I need to understand this part properly...
07:43
Ok
Lemme just read up on this quick..
Should I continue ?
@ronakjain I don't think you can write it exactly like this for a given product..
@Safdar are you talking about my paper clip that I posted ?
@ronakjain yes (and no) the method as a whole.. It is fine to say the change in free energy is so and so.. however, we have only ways to calculate the difference in free energy and not actual values of free energy. [I think]
@ronakjain I am not exactly sure if this is valid..
07:50
@Safdar but the books also calculate the exact value with their method ? Can you tell me whether my method is correct or not ? I just only want to derive the expression for gibbs free energy change and reaction quotient
Ok
So, I will have to talk to someone else
Because from what you state, if G value is positive then, it is reacts [But with what?]
@ronakjain This formula is derived using chemical potential.. Which is currently not taught in syllabus.. that may be why it seems so confusing.. basically, they use dG=Sigma(udN) to prove this.
Wikipedia has a pretty good proof on how this happens.. but you have to keep in mind that it is fine if you don't understand because right now this is out of scope..
But how will you define Gibbs free energy change of reaction when concentration of species are given. For example....
@ronakjain Same way, that is what chemical potential is all about..
It helps you identify the direction of a reaction.. Similar to E in electrochemistry.
07:54
Consider thd reaction....aA + bB = cC + dD. And we are given the concentration of a = (A) of b = (B) and of c = (C) and for d = (D).
@ronakjain I would have to prove it right now, if you wish to understand.. you fine with that?
@Safdar So in this case how will you define gibbs free energy of reaction ?
Ok
You have mathJax? [would make it easier]
then give me a min.. lemme type it out and i'll send it part by part.
07:57
Ok
Let me see....
@Safdar actually I think this is also something like proof of my book though it uses an extra udN
Let me show you
The reaction they have taken is:

$$\ce{\alpha A + \beta B -> \sigma S + \tau T}$$
@ronakjain If this were $\mu$ then it would have been correct.
@RobinSingh Hey.
Wassup.. how's life.
08:03
Going good
Aap batao
@RobinSingh aap? ithna respect kaha se aaya re? accha chal raha hai abhi..
:P
@Safdar this is how my book proves the relation .
@ronakjain what is Po?
Can someone answer that why a group can't a group "exert" +M/-M effect on phenyl ring if it is non-planar to it? And is it just in case of Phenyl ring?
08:05
@Safdar its standard pressure at which Gibbs function is G°
@ronakjain they've over simplified it..
@Safdar ok. To go ahead , tell me that what was problem in ky method which I had derived in room with John sir
@RobinSingh Resonance needs planarity no? how do you expect to overlap properly when there is an angle between the two?
@ronakjain Simply put, your initial assumption is wrong..
whatever happens after doesn't work then..
Are you guys going to give NSEP/NSEC?
@Safdar but why ? That will tell the difference in Gibbs function in between two states. And that will be Gibbs free energy between two states
08:12
@RobinSingh do you really wanna write that for the 3rd time?
@Safdar What?
@ronakjain states.. not reaction co-ordinates [don't mix them up]
@RobinSingh technically those who were in 12th before corona are now 12+ and would be writing for the third time
@Safdar I was in 11th before corona and I never gave NSEP/NSEC
@RobinSingh ok then fine..
@Safdar How did you perform in NSE's in previous years?
08:15
My bad then.. age is pretty difficult to calculate online.. thought you were in 12th+..
@RobinSingh qualified astronomy [then forgot to register for the next round]
@Safdar I had the same confusion when you said that you are 12th prepping
@RobinSingh Well
I've passed 12th officially.. so now I am a....
what am I? other than a human..
@Safdar Delving into philosophy now XD
@Safdar Which book did you solve for organic?
not a dropper, haven't dropped a year.. not a repeater, first attempt.. not in 12th anymore but also not in college.. Hmm..
@Safdar Seems like a nice riddle
08:18
@RobinSingh MS chauhan.
Why not himanshu pandey?
@RobinSingh have both.. faculty told to solve MSC so did that.. now solving HP..
@RobinSingh have a pdf of it.. too lazy actually.
Chalo phir ok bye
08:19
cya,
@RobinSingh is Himanshu Pandey faculty of AIIMS ?
08:46
@Safdar can you help me in a riddle
@Yuvraj I'll try why not..
@Safdar actually Grignard look for the acidic hydrogen for the best,and if it is not there it goes for the lone pair if i have RMgx compound if react it with a ethylene oxide what you feel what would happen?
@Yuvraj Will attack on one side and open the ring..
continue?
So then R-CH2-CH2-OMgBr forms.
09:00
if you hydrolysis it then?
@Yuvraj primary alcohol forms..
but answer says a aldehyde group is formed
in between
Same reaction is given there.. no aldehyde..
sorry i frogot to mention it was with the thf
@Yuvraj as solvent?
09:08
yup
so it would turn R2Mg +MgX_2
@Yuvraj that is also ether right? that is the reason for stabilisation of grignard in medium..
yes there is the ether ?
then?
@ronakjain @ronakjain He is a coaching teacher somewhere in Bhilai-youtube.com/watch?v=ntaILcUw2X8
09:17
@Safdar i got my answer one more question if i react Grignard with a compound who has both alcohol as well as carbonyl group where does it react and why?
@Yuvraj Alcohol..
Acid base reaction is must faster..
*much
with aldehyde and ketonic group?
2 days ago, by Yusuf Hasan
3
A: Mechanism of three-membered lactone hydrolysis in base

SafdarAccording to Organic Chemistry: Second Edition,[1, pg 934](from which I assume that the question was taken): Enantiomerically pure (R)-2-bromopropanoic acid reacts with concentrated sodium hydroxide to give (S)-lactic acid. The reaction goes with inversion and is a typical SN2 reaction—and a goo...

Similar to this
@Yuvraj aldehyde since nucleophilic attack happens at more electrophilic center..
what i feel is rather than electrophilic it would be due to steric hindrance?
@Yuvraj both actually.. ketone is at a disadvantage regarding both..
09:22
ok thanks
@sai-kartik what is your profile pic?
@Safdar Miles Morales
heard of him?
@sai-kartik Spiderman the kid one..
@sai-kartik almost typed assassins creed there :D
09:26
@Safdar lmaooo
so what you doing now?
@sai-kartik Solving physics Q..
ahh nice
Suggestions for good music?
you have any special organic questions?
@Safdar Gryffin(Artist)
for like soft edm
@sai-kartik Anything else? something louder..
09:29
Also have you heard Alec Benjamin's songs
@sai-kartik I'll sleep if I listen to this now..
@sai-kartik Used to.. then heard it too many times and then stopped
@Safdar no no like its the catchy type
but not heavy metal
listen to Bye Bye by gryffin
youll get the idea
@sai-kartik you don't know.. I am at the point where rock might let me fall asleep..
@Safdar what.even.
XD
but just try once
@sai-kartik yeah sure..
09:32
How about the script?
@sai-kartik Think I've already listened to griffin before.. not sure.
@sai-kartik too many times still..
@Safdar gryffin*
aight i gtg now
before i go..
I listened to music for 12 hours straight for the last month..
guys i one more confusion i have in books is if i says phrnol react with hbr do issume medium to be water
5 mins ago, by sai-kartik
you have any special organic questions?
@Safdar dauym
09:33
means neutra;\\\
@Yuvraj It should be mentioned
cus you have two separate reactions
@sai-kartik not really.. I just go with the flow.
@Safdar ohh okay..
there is no mention
our teacher says assume hbr +h2o
09:34
@Yuvraj you can assume water as solvent but what you get would be tri-substituted bromophenol.. [i think]
like Br on o- and p- positions
@Safdar why? h in hbr does not react with oh?
@sai-kartik is there a difference?
@Yuvraj after that?
@Yuvraj positive charge cannot come on benzene right? SN2 also doesn't work I think..
@Safdar can you show the mechanism
@Yuvraj Is it fine if this happens later in the evening?
... or wait.
ok around 6
by the way do not pping my brother
it is his account i use it usually for my queries
09:37
@Yuvraj Aahh..
I understand now.. It was so confusing..
@Safdar sorry i should have told you before
everybody feels the same
@Yuvraj no no its fine.. Btw its no reaction.. phenol doesn't react what I said was for Br2
@Yuvraj why do you not have your own account?
@Safdar it do not have my own phone or pc
@Yuvraj You are using chrome right? Can't you just make a different user on it?
it is with them so creating my account is of no use
09:41
@Yuvraj who? them??
two brothers
b the way can you tell me why do not they react?
@Yuvraj Same reason as message above this..
thanks though
@Yuvraj no prob.. Why not ask your brother though? just asking..
@Yuvraj Which grade are you in?
Alright then gotta go.. I would be online but that is b/c I have it open in another tab. do not expect a reply when you ping me.
 
2 hours later…
11:38
If anyone is interested, I've asked that question on the main site:
0
Q: Mechanism for the addition of hydrogen iodide to 3,3‐dimethylbut‐1‐yne

Guru VishnuThe following reaction mechanism was given as a solution to a solved problem in my textbook1 for the addition of hydrogen iodide to 3,3‐dimethylbut‐1‐yne: It can be seen that that 2,2-diiodo-3,3-dimethylbutane (a geminal dihalide) is the product according to this mechanism. I arrived at a differ...

Not advertising though :P
12:11
@GuruVishnu +1.
@GuruVishnu I've added a comment.. that should be the reason..
not advertising here as well :P
13:04
@CaptainBohemian what brings you here?
13:15
@satan29 you
@YusufHasan hey..
13:31
@Safdar About your issue...I don't see if we can do much without reporting to mods or confronting
@YusufHasan you sure
13:51
Yes...A third option would be reporting the specific comments and/or answers where the condescending stuff has been said..It might be that the mods don't directly question you, or it bypasses them...Either way, flagging stuff seems the most indirect way to do the reporting, if a mod doesn't have to be invloved directly
14:02
@CaptainBohemian aww
@Safdar That definitely solved the problem. But I'm unable to find a green tick to accept it. Thank you :-)
@GuruVishnu I'll add an answer later, if no one else does.. currently not free..
@satan29 Thank you. That wasn't needed though. Seems it finally became an ad :/
@Safdar No problem! Understood.
14:33
Are unacademy's classes good for phy?
15:04
@Safdar For that benzaldehyde thing, I didn't pay attention closely but the phenol only should migrate as it can stabilize the TS by it's electron rich nature
This is the TS^
This is how it can stabilize
 
2 hours later…
17:10
Hi guys I am facing problem with this rather simple looking question
The D is removed I assume.
the double bond is on the right side
E2 occurs anti periplanar
so is Br is towards us, then the H/D away from us is removed.
@satan29 A bit too slow? :P
@HrishabhNayal remember that in E2 elimination, the X and H/D have to be anti-periplanar
Oh thanks
17:12
@satan29 Bzzt
Btw why tho
Why anti-periplanar
You cant remove H, since that is on the same side of the plane as Br
@HrishabhNayal steric hindrance due to halogen would be a simple explanation..
@Safdar Ok
And what about E1?
E1 is simply by CC...
17:14
@HrishabhNayal Carbocation formation happens.. that is RDS.. so no difference
@satan29 you answer. one of us at a time..
So in E1 what would have happend in the above question?
CC forms--->rearranges(if possible)
so here i believe it will be a hydride-shift first
@satan29 right there seems to be a possibility for 3° there so H shift?
@satan29 One doubt though.. Will double bond go up or down after that?
@Safdar didnt get you?
17:19
Closer or away from D atom?
@satan29 One min.. I'll share an image.. which product would be more likely there?
@HrishabhNayal it will go to the left
@satan29 why?
isnt it simply more stable there?
due to HC?
@satan29 further from D?
@satan29 HC?
17:20
@HrishabhNayal yes
@satan29 D does show HC.. but I agree with you..
@HrishabhNayal hyper conjugation
@Safdar cause D has less stable HCs?
@HrishabhNayal the bond is harder to break..so yeah..
And then finally an H + from the adjacent carbon, to yield an alkene
@Safdar Although i dont understand this:
17:23
@satan29 Ok
Thanks guys!
If you have propyl bromide Br on C1 and D on C2, the whole molecule rotates so that H becomes antiperiplanar to Br before attacking.
@satan29 you don't understand HC or D being less stable?
isnt Hyper-conjugation a kind of overlap between an sp3 orbital and a vacant p? (in case of carbocations)
@satan29 yeah.. not exact overlap but sort of.
so then I dont see how D "shows hyper-conjugation"
@satan29 why not?
Its exactly similar to H. they are isotopes after all.
17:27
you require a h/D bonded to an sp3 carbon
Right??
in hyperconjugation
@satan29 yep.
@satan29 btw, here HC takes place after bond formation K..
ok wait i think now i get your point
the possibility of HC with D is if the CC didnt rearrange
@satan29 Yeah/
my bad. I was thinking you were shifting the CC to the right, and then claiming that HC happens with D. Which baffled me.
@satan29 oh. *thumbs_up
17:31
although, say this was E1
"nd then finally an H + from the adjacent carbon, to yield an alkene" in this step
kaha se nikalega H?
@satan29 We did do a hydride shift so it is there, but wouldn't the reaction happen to the other side?
I think this is the time to draw structures...
CH3 on right is D.. couldn't get that.
@satan29
yes ofcourse those are the two products
my queston was, which one will be major?
@satan29 down one.
since C-D bond is harder to break so less effective HC
17:41
and another question, how did you know that H- after shift is in Dashed position?
@Safdar Ah!
@satan29 can be either.. did not want to draw four structures.
yeah haha thought so

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