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8:05 PM
Any1 still there?
 
what is it ?
 
Consider this
Benzene plus 2 methyl butanol with bf3 and heat as reagent
What is the major product
@Tanuj you there?
 
Isn't it friedel crafts alkylation ?
 
How come?
 
BF3 acts a lewis acid instead of AlCl3
 
8:17 PM
But bf3 won't act as a Lewis acid now why would it there is already back bonding
It increases e density on bf3
Would that just make the rate slower
 
and you should form the most stable carbocation from 2 methylbutanol which would then do the electrophilic substitution
I guess yes , it would have the effect ,if any , on the rate , maybe cause its a definetly a weaker lewis acid than AlCl3
 
Hmm yea that should definitely be the case
 
alright .
 
Wouldn't the major product then be just benzene with pentyl as a substitute nt
With benzene at the second c
 
what ?
 
8:23 PM
Major product
 
according to me , the carbon attached to the OH should get attached to the benzene , everything else , remaining unchanged.
 
Oh won't leave?
 
why ?
Whats the answer given ?
 
If oh doesn't leave how do we get a carbonation
The ques itself asks for the no of monochloro products including stereoisomerism when cl2 reacts with the major product of the above react in sunlight
So first of all what would be the major product
If this is fc alkylation then there should be a carbonation now that will be formed only when oh leaves right?
And then after rearrangement we get the product I wrote earloer
??
 
Of course the OH would leave
you're correct
no but it wouldn't be a pentyl group
it should be 2 methyl-butyl
 
8:32 PM
Oh shit my bad
What the hell am I doing
I must sleep it's getting late lol
 
could you take it on from here ?
 
Yup
 
yeah same ! :D
 
Even got the ans
4
 
awesome !
 
8:32 PM
Thanks
 
good night !
sure thing man
 
Could you help me with a couple of mire things
*more
 
yeah sure
 
Not silly ones like this I promise
 
right now ?
 
8:33 PM
Yup
10min max
 
okay make it quick I'm really mid sleep
 
I have a test tomorrow so it's kind of urgent ya know
Thanks a lot
Can fc acylation be used to obatin
Para acetate acetophenone
It shouldn't be right?
That deactivating grp should be meta directing right?
 
should be as you think it
 
Ya then the ans is wrong
 
lets see
 
8:38 PM
The reason why is more nucleophilic than br is cz in cl the e density is more right cz it has a small size?
Right?
 
i dont think electronegativity has to do anything with size
 
Than what would be the reason?
 
Br- ion is bulky in size and since we associate nucleophilicity with movement of ions , Cl- due to smaller size will have much more mobility and thus would be a better nucleophile
 
Oh k thanks
Consider cyclohexane
On two opposite c there are ch3
On the two carbon be them there is a double bond
Only one double bond though
We react it with os o4
We will get syn di hydroxylation right?
 
yea must be
 
8:48 PM
Till that point it was fine but then the question
Again reacts them with nahi and h20
*naoh
And yet the product remains the same
What happens here?
 
react what with NaOH and H2O ?
the intial reactant or the cis prod ?
 
The product which we got after di hydroxylation
Via prod
*cis prod
 
it may be because as the medium we have now is basic (NaOH) , and the reactant itself is a base , with deficiency of any acidic specie , the product would remain same
 
So that was given just to confuse us?
 
hmm , not exactly , but you could say that
its still testing your knowledge
FIITJEE test if im guessing correctly right ?
 
8:52 PM
Yea you could say that
(ph)3c - ch=ch2
Yup
 
Bro really gotta go now .
 
This with 1 eq of br2
How come the final product is aromatic
This really is the last ome
If a substance has phenyl anywhere in it do we term that as aromatic?
 
you could say that , but its a very very lose way to say it
your molecule basically has to fulfill the Huckel's rule
 
Yea but in a new paper would you mark that as aromatic
*mcq paper
 
with 3 phenyl rings , you have the value of n as 4 to satisfy the huckels rule so yea
 
8:58 PM
One final thing if you have the time. Consider cyclopentane with one ch3 substituted . We react it with 1 eq. Of cl2 in sunlight. We get a mixture of how many stereoisomerism?
Hmm yea it does have n =4
 
2 ?
 
Nah
10
 
oh i thought benzene
 
How the hell does one make 10 isomers in the middle of an exam
Ain't that too lengthy?
 
wait let me see
 
9:05 PM
?
 
yup
just getting 8
 
Isn't that too lengthy?
Check the mode of linkage for each c check possible kesi forms it drove me mad
*meso
I ended up with 7 somehow
 
thats surely a question for the main site !
 
@Tanuj I gotta go now.(the exams at 9 30 tomorrow) Thank you so much for helping me. You are a life saver.
@Tanuj maybe tomorrow
 
Welcome
 
 
1 hour later…
10:25 PM
People helping each other.
Without teasing, even
WHAT THE HELL IS WRONG WITH THIS CHAT
-2
Q: Which chemicals found in fragrances are the most dangerous for the human health?

Georgios PligoropoulosThis is an appeal to the community to help with a case where fragrance is a serious suspect for a cancer case. The only two facts are that the fragrances were not properly tested and the man who suffered from cancer was using these fragrances for 4-5 times daily. Now the cancer was on the lymph ...

Wow, this is probably the government of Atlantis asking for help
Nice. The median score for the last 7 questions is -2.
Aaand the newest question doesn't help
 
11:11 PM
@orthocresol Tanks for your answer! So the oxonium-resonance-structure stabilize the whole S<sub>N</sub>1 intermediat and so we can assume that also the S<sub>N</sub>1-mechanism happens also at a "big" amount? — Nilsfrank99 Apr 18 '16 at 15:17
Can a mod please edit that comment? It's ruining an awesome thread
Helicopters in advance
@Mart remember I had this comment flag campaign with one member that flagged unnecessary comments on the oldest posts on the site?
I wanna continue, but the problem is I don't remember where I left off
8
A: Why are there so many poor questions?

AliceDI also have noticed a trend towards poor-quality questions becoming abundant. I think there are several reasons for the overall quality being relatively poor at this stage: The number of active reviewers has dropped; at this time there are 57 close-voted questions in the review pane. It has bee...

Good grief. 57 close reviews.
Reviewer paradise and hell at the same time
 
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