Chemical Forums
Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: Molly71 on January 05, 2013, 06:06:33 AM
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suggest structures for the following A,B,C,D :
(question is attached)
thanks (:
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http://www.chemicalforums.com/index.php?topic=57.0 - Forum rules require that you try and give some thought to your question before posting. Do you recognise any of the reagents and what they may do?
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Oh im sorry!
I thinks ive managed A and B, Im really not sure though..
I find the subject very difficult, so I need a bit of help and explenation.. :-\
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Have a look here http://en.wikipedia.org/wiki/Williamson_ether_synthesis (http://en.wikipedia.org/wiki/Williamson_ether_synthesis) and see if you can relate it to your problem.
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it helps a bit I guess.. but there is still too much that i dont understand..
can't figure out this problem..Im quite new in the chemistry buisness.. :-\ ::)
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Why can't you apply what's on that link to your problem.
Hint: what is the reaction of sodium metal with alcohols?
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Na seems like an odd choice (although it should work). Are you sure that you copied down the problem correctly?
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Ok! I think I've managed C as well! thanks alot! (;
I still don't have D.. im thinking ch3 will bond and I is a leaving group?..
And I'm sure I coppied the question correctly! it's Na for sure ::)
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Iodide ion is a great leaving group, so you seem to be on safe ground there. What do you propose as the nucleophile?
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mmm maybe I got it wrong then.. C is not the nucleophile?
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The carbon atom of CH3I is a plausible electrophilic center. Nucleophiles need at least one lone pair of electrons.
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mmm maybe I got it wrong then.. C is not the nucleophile?
Have another look at the link I posted and see if you can determine what the nucleophile is.
It shows you in the first reaction.
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Yap! I think I got it now (:
Thanks alot everybody!