Based on your result comment on the relative “activating strength” of methoxy and hydroxy groups in electrophilic aromatic substitution.
(product being 5-Bromovanillin) from reactin standard Vanillin with Acetic acid, Hydrobromic acid, and Potassium Bromate in a directive effect reaction
activation or deactivation of the benzene ring toward
electrophilic substitution may be correlated with the electron
donating or electron withdrawing influence of the
substituents.
The substituent effects of P-hydroxy and p-methoxy compounds is
similar, but ortho compounds it is different, o-methoxy is having
more comared to o-hydroxy compound.here we have to consider the
meta effect of aldehyde group.
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