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![[Post New]](/templates/default/images/icon_minipost_new.gif) 12 Apr 2008 23:08:47 IST
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in which of the following the resonance of NH2 is possible why? benzyl amine , 1-aminopropane , ethyl amine , p- touidine give the structure also
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p -toludine
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![[Post New]](/templates/default/images/icon_minipost_new.gif) 12 Apr 2008 23:17:02 IST
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how give reason i give u rates
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![[Post New]](/templates/default/images/icon_minipost_new.gif) 12 Apr 2008 23:20:40 IST
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in benzyl amine Ph--CH--CH2--NH2 1 2 there is no conjugation of N lone pair with the ring as there is no double bond between C1 and C2 rest 2 are saturated structures
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![[Post New]](/templates/default/images/icon_minipost_new.gif) 12 Apr 2008 23:29:03 IST
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ashish u give me ans as 4 and give stuucture and explanation for 1
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![[Post New]](/templates/default/images/icon_minipost_new.gif) 12 Apr 2008 23:30:24 IST
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there is no other option left except 4
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![[Post New]](/templates/default/images/icon_minipost_new.gif) 12 Apr 2008 23:31:37 IST
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well p toludine CH3 - Ph - NH2 clearly lone pairs of N are in conjugation with the ring
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![[Post New]](/templates/default/images/icon_minipost_new.gif) 12 Apr 2008 23:32:33 IST
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i didn't get that rest 2 are saturated i know what are saturated compds but how u have eliminated them
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