Betrekkingen tusschen de constitutie van organische verbindingen en den invloed van het hydroxyl-ion bij hydrolyse

Rates of saponification ofα-chlorotoluene,αα-dichlorotoluene andα,α,αtrichlorotoluene and of their ortho, meta, and para isomers of halogen, nitro methyl and carboxylic derivatives in neutral, alkaline or acid medium were measured. The velocity of the hydrolysis in the different ranges of pH could be correlated with the effect of substituents present in the aromatic compounds and with the character of the catalysts involved in the reactions. The results obtained when saponifying in basic medium could be reasonablyexplained by the 'alternating polarity effect' (valid at that time) and by assuming a general electron shift in the direction of the negative substituent.

Saved in:
Bibliographic Details
Main Author: Weber, A.P.
Other Authors: Olivier, S.C.J.
Format: Doctoral thesis biblioteca
Language:Dutch
Subjects:hydrolysis, organic compounds, hydrolyse, organische verbindingen,
Online Access:https://research.wur.nl/en/publications/betrekkingen-tusschen-de-constitutie-van-organische-verbindingen-
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Rates of saponification ofα-chlorotoluene,αα-dichlorotoluene andα,α,αtrichlorotoluene and of their ortho, meta, and para isomers of halogen, nitro methyl and carboxylic derivatives in neutral, alkaline or acid medium were measured. The velocity of the hydrolysis in the different ranges of pH could be correlated with the effect of substituents present in the aromatic compounds and with the character of the catalysts involved in the reactions. The results obtained when saponifying in basic medium could be reasonablyexplained by the 'alternating polarity effect' (valid at that time) and by assuming a general electron shift in the direction of the negative substituent.