1well check for tautomers guys at this level this should work .
tautomerise and then react it NH2OH reacts with aldehydes and ketones
Hopefully this solves your query
1dude , if it would hv been so simple , i wouldn't hv given it.
Make a better try try , please.
1k. seems, no one is being interested in it.
Let me bring in the actual question.
Actually , here , 1st two compounds i.e. phenol and 1,3 di hydroxy benzene doesn't react at all !
while the 3rd one i.e. the trihydroxy compound forms oxime with NH2OH . why is it so ?
19i cannot make out anything ! really strange !! may be , i am not thinking much !! anyways, i am really interested in getting the complete answer from mr.aieeee.
1if we tautomerise each of the three the third one will be most stable
so may be it is the only one which will tautomerise
maybe......
