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@Dexter
Note for OP
+solved @user1 @user2... to close the thread when your doubt is solved. Mention the users who helped you solve the doubt. This will be added to their stats.Is it:
1. Hoffman Bromamide to get NH2 instead of conh2
2.Diazonium salt formation
3. Chlorine gets added replacing N2+Cl-
4. Elimination
5. Addition of Br2 via free radical mechanism?
nice input!
did you check out what was said above? we good?
I guess 2 is formation of alcohol because it is not aromatic, wait I have to check
nvm
neither alcohol nor diazonium salt
Chemistry LibreTexts
Reaction of Amines with Nitrous Acid
Nitrous acid reacts with aliphatic amines in a fashion that provides a useful test for distinguishing primary, secondary and tertiary amines.
That is just NO2, in the question it is NaNO2+HCl
HNO2
NaNO2 + HCl gives you HNO2 which makes NO+ electrophile
Bingo
It forms hno2 in situ
yup thanks
what does aq nahco3 do though
James Ashenhurst
Master Organic Chemistry
Reagent Friday: NBS (N-Bromo Succinimide)
NBS has two major uses in Org 1/ Org 2: allylic bromination (the most common) and also as a replacement for Br2 in the formation of bromohydrins.
check master org chem when in doubt
and a quick google search just mentions that silica and nahco3 helps yield
we good>
+solved @!Nimay¡ @SirLancelotDuLac
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