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and ... ? It is not even a correct compound.
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nopes,,, I dont' think ethyl alcohol can be the product. Though the answer I'm getting is bizarre. Nilesh, you tell the answer... If it matches (rare chance), I'll give you the key-in. The only problem, is excess of Grigenard Reagent! It's causing recursion by whichever way I try to solve it down.
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hehe... Now, I'll have to say: This site is doomed!. No worthy question and obviously no absolute answers in return... btw, remove that link what_the_F dear... I don't wish to have any sorta crap there.
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Write it all over again. whenever sitting idle, just start revising them. And don't care about other reactions, start with limited reactions. You will get through.
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Solomons is more than more than enough.. There is no need to refer any other book. I assure that all other books will look scanty in front of it.
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WTH....... instead of revolving your mind in a seperate world you should come back to holy earth.. wings are tethered as soon as it crosses the barriers.. I'm not being rude.
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yaar, now this is very simple. This is formation of carbonyl compounds. Refer your notes, I can't supply with mechanism.
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You can refer to other 'similar' threads. I assure there are more than thousands.
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Iteration in question is required. Nomenclature is wrong
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When you can Google it, what do you Google for?
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You should have used an asterisk instead of dot to represent isotope, I thought about radical half the time.. Just a suggestion. Someone has already answered it.
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hmm.. yeah, I read about it in Co-ordination compounds. Can't write it in exact words because I've not still learn it yet..
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instead of insti;s modules for notes, you can prefer a book.. market is flooded with Morrison, OP Tondon, Solomons, Arihant, Jones and hell others.
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dat's is what I'm wondering about.. not heard of this.. google is there anyways.
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hemi acetal which is formed is not stable enough to remain in that state and thus proceeds for formation of acetal.. and acetal formed is not stable enough to exhibit that structure and it breaks off with H2O, bringing back aldehyde.. that's y it gives 'split second' advantage by dioxolane formation.
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Nice one Dembalya Ray, I read a single page of Arihant at my insit's library and that was reduction of acyl chlorides.. exactly same words as I remember.. hats off
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