Talk:Methyl benzoate

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Untitled

The page notes the fact that methyl benzoate has a pleasant and potentially useful odor. Um... maybe it was our stuff in the lab, but I found the smell very unpleasant, and downright repugnant. Any other thoughts on that one?

I don't think it has much smell at all - but then I'm an organic chemist, who worked a lot with thiols, so I lost my sense of smell a long time ago.... Walkerma 05:30, 26 July 2007 (UTC)[reply]

Whether something is pleasant smelling is quite dependent on concentration. Low concentrations of methyl benzoate seem rather sweet smelling, though sniffing a bottle of pure compounds is likely to be stomach turning. —Preceding unsigned comment added by 128.210.187.174 (talk) 22:31, 25 March 2009 (UTC)[reply]

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This article talk page was automatically added with {{WikiProject Food and drink}} banner as it falls under Category:Food or one of its subcategories. If you find this addition an error, Kindly undo the changes and update the inappropriate categories if needed. The bot was instructed to tagg these articles upon consenus from WikiProject Food and drink. You can find the related request for tagging here . Maximum and careful attention was done to avoid any wrongly tagging any categories , but mistakes may happen... If you have concerns , please inform on the project talk page -- TinucherianBot (talk) 01:08, 4 July 2008 (UTC)[reply]

Who attacks?

Electrophiles are electron-deficient species. Essentially with a hole waiting to be filled by electrons. The benzene ring (the nucleophile) pushes its electrons to fill that hole. It's not really a matter of which is more mobile. —Preceding unsigned comment added by 128.210.187.174 (talk) 22:29, 25 March 2009 (UTC)[reply]

Include Synonym?

AKA "Oil of Niobe" - http://www.chemindustry.com/chemicals/0218151.html Ileanadu (talk) 03:10, 22 March 2011 (UTC)[reply]