given , I edited the post.
9 Answers
voldy
·2008-11-03 10:22:15
isn't a H there on N ?
assuming it's there . this should be it.
well , first we get an substituted amide , which on acid hydrolysis gives. these products. I think.
Abhishek Priyam
·2008-11-03 10:42:56
But options are not matching Ok i am posting the answer then also if u will explain it will be fine.
voldy
·2008-11-03 10:49:02
there is an attack on the electrophilic carbon . by the alcohol . I'll post the mechanism in a mo.
voldy
·2008-11-03 10:59:34
this should clear it. the hydrolysis part is easy , you should be able to do ti.