Chemical Forums
Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: lrisNil on February 20, 2015, 12:52:25 AM
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Is Benzyl Alcohol (Benzene ring with CH2OH attached) a meta director? OR is it a ortho/para director?
I know the O deactivates (suggests meta) and alkyl groups activate (suggests ortho/para) but this group has both so I became confused!
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Apparently it is electronically neutral, i.e. the effects you mention cancel out.
Hammett constants: σm = σp = 0.00; source: Hansch Chem Rev 1991, 91, 165-195 Link (http://pubs.acs.org/doi/pdf/10.1021/cr00002a004)
So expect nasty mixtures...
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Thanks Dan! C:
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I thought this was an interesting question, although I cannot provide a definitive answer. I thought Friedel-Crafts reaction on the alcohol might be problematic (I did encounter a Russian ref to its nitration though). I thought I recalled a problem asking for the products of nitration of benzyl acetate and it was an o/p-director. I tried to confirm this, but I cannot determine the ratio of products from this reaction. It seems to be cited for the preparation of the para-nitro product.
The nitration of benzyl chloride would seem as though it may have a similar profile of an electron withdrawing chloride to counter electron donation. Again, I was unable to determine the ratio of products, but references seem as though this is used to prepare the para isomer(?).
Now, I want to take one step back and refer to the nitration of toluene. Although it is an o/p-director, the ratio of o,m, & p-isomers is ~63:3:34. Benzaldehyde gives a ~19:72:9 ratio.
I appreciate the opinion of Dan on this question and it may well be instructive, but I also think it may still be mainly an o/p-director. What might be as interesting would be the kinetics of any Friedel-Crafts reaction. Is or are they activators, deactivators, or neutral?
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Thank you orgopete, I've decided to not use this group when trying to solve a synthesis problem, but it probably is o/p according to my googling (some say o/p, few say meta) :P