etoh

right only i think :P (since i think, so it may be wrong also... :P :P)

richa i can give u another explanation for the reason for the ans is c.

in the option C the product is formed by the elimination of the hydrogen at the saturated Carbon .therefore the C-H bond is weaker when compared to the bond --C-H therefore it is easy to break the C-H bond.pls reply richa if i blabbered .

http://targetiit.com/iit_jee_forum/posts/important_information_2774.html

Richa i was talking about this

yup ans is C.

pls reason it sky .

wait subash is it dat much bulkier base to give hofmans product.??????????

neways hofmans product is c.

i think de same reason was given in my last post.tx for posting this sky.i want to confirm whether i was rite or rong.

try my other questions too

arey ek hi baat hai ~!#~$#~^%%&^!!!!!!!!!!!

i think so also

arey what is ur explanation corect or not

arey ... u put it in 4th position ... same hi hai dono ka structure...

arey ... u put it in 4th position ... same hi hai dono ka structure...

i think sky u r correct

a and c can be formed but c is more stable due to resonance so c is the major product. but wat is the ans richa.

no

[2]

today is not my day :(

@manipal correct could u explain how u get it?

but only possible ans
d to sapne bhi nahi aaya

c kaise aaya

CH₃O^- is a good nucleophile
and goes via SN₂in CH₃OH medium

copyright my notes

tell me if u wanna table for it

is answer (D)

ans is c only @sankara c is not at all resonance stablized @mani sn2 does not give elimination