Chemical Forums
Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: limonade on August 12, 2013, 10:47:18 PM
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I was asked to give the organic aldol condensation products as in the following question.
I have drawn out the mechanisms on scratch paper. It makes sense to me. I gave the dehydration products as shown in the picture and it counted me as wrong. I have no idea if it wants the neutral aldo product before it undergoes dehydration. It won't tell me what I did wrong, chemically speaking not program wise, and I would like to know otherwise I just might make the same mistake again, if I have made any. Any help greatly appreciated. Thanks
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I would think the product would be
unless it is asking for the product before loss of water. But the aldol condensation is the synthesis of conjugated carbonyl compounds.
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The problem is your cyclohexenone - it will not form - draw out the mechanism, can you see why?
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Yep. I see it now. Its not a conjugated diene. x/
Thank you