00:01
Thanks welcome here in this question why allyle halides are more reactive when compared with alkyl halides towards nucleophilic substitution reaction.
00:18
So if you see here allyle halides, ch2 double wound, ch, ch, ch, ch2, cl, if you see, this one is cl, if you see, this one is cl.
00:30
When this cl gets out there, here, positive charge is produced.
00:37
Here there is a resonance structure is present.
00:41
So due to presence of adjacent double bond, there is a resonance stabilized carbocardian is produced.
00:49
Resonance stabilized.
00:54
So that's why it is more reactive when compared with alkyl halets.
00:59
So in alkyl halets, there is no...