Organic Chemistry

1

vector ·2009-03-09 08:24:48

d i think

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Vivek ·2009-03-09 08:30:29

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

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1

arjita ·2009-03-09 08:37:29

ans is c

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vector ·2009-03-09 08:39:49

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

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1

pavanmalhra ·2009-03-09 08:57:13

i think its c

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1

Vivek ·2009-03-09 09:33:33

pavan - ans is d

richa's explanation is correct

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1

vector ·2009-03-09 09:35:36

:)

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33

Abhishek Priyam ·2009-03-09 09:37:01

d..
hmm...

:)

wah!! good...

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6

Aakash Sharawat ·2009-03-11 21:17:42

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

cheers!!!!!!!!

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1

Vivek ·2009-03-12 10:24:50

@aki

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

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1

vector ·2009-03-14 00:47:42

no pink

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Abhishek Priyam ·2009-03-14 07:43:37

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

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