Organic help @abbot
Of the five isomeric hexanes,the isomer that can produce 2 monochlorinated products is?
Well what are the five possible isomeric hexanes, do you know?
I can try
theres hexane, 2,2-dimethylbutane...
2,3-dimethylbutane...
do you remember what we dicussed yday? :)
Yep :)
so we need only 2 diff H atoms here.
So, which ones can we rule out? Let me draw them out 4 u, it might help
|dw:1394599574627:dw|
|dw:1394599764137:dw|
Uh, is that a circle? Lol
I meant a tick mark.
Oh. Well, that one is correct. haha.
Yey :)
2. The compund formed as a result of oxidation of ethyl benzene by KMnO4 is:
carboxylic acid.
How to figure that out?
you mean, ethylene benzene??
I mean how u got Carboxylic acid? It is not there in options lol
oh wait its there my bad :/
so how u get carboxylic acid?
I don't remember the detailed mechanism, but generally KMnO\(_4 \) and K\(_2\)Cr\(_2\)O\(_7\) in an acid, oxidize aromatic alkyl groups to carboxylic groups or ketones.
But for safety purposes, potassium permanganate is used since it is safer than potassium dichromate
so why acid here and not ketone?
I really don't think that for intro to organic, you need to know the details of it's mechanism.
so why acid here and not ketone?
well, this is also a radical reaction. so, you want to form the more stable product, and it is more stable at the C2 than it would be at the C1 methyl.
if you are REALLY interested in the mechanism or detailed explanation of this, you can look in a advance o-chem book, or graduate level textbook.
oh ok :)
for practical purposes, it generally cleaves the CH\(_2\) group adjacent to the benzene.
also, note that you need a free hydrogen, since remember, this is a radical rxn.
3. Toluene is nitrated and the resulting product is reduced with tin and HCl. The product so obtained is diazotised and then heated with cuprous bromide. Reaction mixture so formed contains?
Have you learned about ortho, meta, para?
activating and deactivating groups.
Yes.
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