Reimer-Tiemann reaction involves an aryl carbanion/enolate anion and also -"CCl"_(3) derived from the action of strong bases on CHCl_(3), though the latter has only a transient existence decomposing to "CCl"_(2), a highly electron deficient electrophile that attacks the aromatic nucleus, the product from phenoxideion is after acidification, very largely the o-aldehyde plus just a small amount of p-isomer. The product of the reaction in the reaction in the above paragraph is largely

Reimer-Tiemann reaction involves an aryl carbanion/enolate anion and a

1.	Reimer-Tiemann reaction involves an aryl carbanion/enolate anion and also -"CCl"_(3) derived from the action of strong bases on CHCl_(3), though the latter has only a transient existence decomposing to "CCl"_(2), a highly electron deficient electrophile that attacks the aromatic nucleus, the product from phenoxideion is after acidification, very largely the o-aldehyde plus just a small amount of p-isomer. The product of the reaction in the reaction in the above paragraph is largely
Answer» m-salicylaldehyde p-salicylaldehyde o-salicylaldehyde NONE of the above ANSWER :C