Epoxide

........................................................................
.......................................................................
no the answer is not C

12 Answers

1
vector ·

d i think

1
Vivek ·

ya but why does NaOH have more preference to act as nucleophile when water is solvent and is present in larger qty?

1
arjita ·

ans is c

1
vector ·

ya but nucleophilicity of water molecule is very low it cant break epoxide ring if there would ve been a better nu as solvent then the major product would ve been changed

1
pavanmalhra ·

i think its c

1
Vivek ·

pavan - ans is d

richa's explanation is correct

1
vector ·

:)

33
Abhishek Priyam ·

d..
hmm...

:)

wah!! good...

6
Aakash Sharawat ·

therefore the answer is B according to the SN1 mechanism in case of a 3° carbocation formation!!!!!!!!!

cheers!!!!!!!!

1
Vivek ·

@aki

what you've shown takes place in acidic medium,in basic medium carbocation is formed at least sterically hindered position

1
vector ·

no pink

33
Abhishek Priyam ·

d hi answer hai... to ye aki B kaise laya...

C+ banane ke baad OH- frm NaOH attack karega... na ki H2O as she had expalined in post5 ..

haan bhaiya pink kar dijiye... :P

Your Answer

Close [X]