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![[Post New]](/templates/default/images/icon_minipost_new.gif) 6 Apr 2008 11:17:42 IST
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6 Apr 2008 12:27:02 IST
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is the answer
2)
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6 Apr 2008 14:00:33 IST
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yes... can u help me with the solution.. what do u get as Y ??
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6 Apr 2008 14:16:20 IST
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it might sound foolish but it was more of the intelligent guesses
see u must get tert-alcohol, so 1 option in discarded
now when an amine(as clear from given compound) reacts with NaNO2 in HCl, the no of C atoms in product does not change
this is obeyed only by 2
though i wud try to get a more correct explanation if i cud
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6 Apr 2008 21:39:15 IST
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it is diazidisation rxn of alkyl amine.the N2Cl formed is unstable due to the alkly grp and gets converted into OH grp.
try writing a tert alcohol with 5 C and u will get 2)
if it was aryl grp then N2Cl grp is stable and is converted into OH only on addition of water.
hope this helps
!!!!!!!!!!!!!!!!!!!
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Varsha
be cool,
tomorrow is what we make it today,
so if u can dream it , u can make it .
life is an ice cream ,eat it before it melts away!!!!!!!!!
    
 
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6 Apr 2008 22:18:58 IST
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@ varsha
can u please let me know the structure of given compds
and as u said that alkyl amine on diazotisation gives alcohol
i wud just like to correct u here that only pri- amines give alcohols whereas sec-amines give N,N-nitroso compds and tert-amines give a mixture of acids
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