Hydroxymethyl compounds have a substituent of #-ch_2-oh#, so i'd say that compounds with those functional groups will be classified as hydroxymethyl compounds. Here's what i get. The general equation for the dissociation of a carboxylic acid is r-cooh + h_2o ⇌ r-coo^- + h_3o^+ all we have to do is write the

Moreover, element names aren't capitalized unless at the beginning of a sentence. We write iron (ii) hydroxide instead of just iron. No, the oh group in phenol is by definition at c1. > the structure of phenol is you can draw the structure like this: Phenol2 however, the structure is not meta-phenol. It is phenol because the ring. Oxides that form neither an acid nor a base, in combination with water.

Phenol2 however, the structure is not meta-phenol. It is phenol because the ring. Oxides that form neither an acid nor a base, in combination with water. Acid oxides will react with water to ultimately give off h^+: Sulphur trioxide so_3 will form sulfuric acid: So_3 (g) + h_2o (l).

So_3 (g) + h_2o (l).