scholarly journals The Kinetics of the decomposition of chloral and its catalysis by iodine

The introduction of chlorine atoms into organic compounds causes marked changes in properties which can often be explained in terms of a displacement of electrons under the influence of the substituent. It is an interesting question how far these influences will show themselves in the kinetic behaviour of the substituted molecules. Accordingly the thermal decomposition of chloral and its catalysis by iodine have been studied. The decomposition is a homogeneous gaseous reaction which can be compared with the decomposition of acetaldehyde and propionic aldehyde. Apparatus The apparatus was of the usual type, with a silica reaction vessel heated in an electric furnace. A tube led to a capillary mercury manometer outside the furnace, and the course of the reaction was followed by observing the rate of pressure increase. In view of the relatively high boiling point of chloral it was necessary to keep all the connecting tubes heated to 80°-90° C. Considerable difficulty was experienced with the lubricants for the stop-cocks operating at this temperature. A special high temperature vapourless grease was used, but even this showed a tendency to run and foul the connecting tubes. The reaction products also tended to foul the apparatus so that frequent cleaning of the whole, including the manometer and the mercury pump, was required.

The thermal decomposition of formaldehyde has been studied for comparison with the decomposition of other simple aldehydes. In the decomposition of acetaldehyde the kinetics of the reaction have led to the hypothesis of the existence of a limited number of different activated states of the molecule. It was of interest to determine whether the kinetics for the simpler molecule of formaldehyde correspond to a smaller number of modes of activation. Experimental Results The experimental method was that described previously. Formaldehyde vapour was introduced into the reaction vessel by heating paraformaldehyde. To prevent condensation in parts of the apparatus outside the furnance, all these were kept above 100° C with heated nichrome wire, a special high temperature grease being used for the taps. As the reaction was unaffected by the presence of water vapour (Tables I and Ii) elaborate drying of the formaldehyde was not undertaken. Care was taken to avoid traces of air which interfere with the reaction. The vapour first given off from a fresh sample of parahyde which had been in use for some time.


1983 ◽  
Vol 2 (12) ◽  
pp. 1891-1894 ◽  
Author(s):  
M. A. Ring ◽  
H. E. O'Neal ◽  
S. F. Rickborn ◽  
B. A. Sawrey

2019 ◽  
Vol 37 (1) ◽  
pp. 1133-1141 ◽  
Author(s):  
P. Sela ◽  
S. Peukert ◽  
J. Herzler ◽  
Y. Sakai ◽  
M. Fikri ◽  
...  

In investigating the rates of chemical reactions, gaseous systems are to be preferred on account of their simplicity. The investigation of the thermal decomposition of organic compounds in the gaseous state possesses the added advantage that there is only one reactant. The present investigation deals with the thermal decomposition of gaseous methyl formate. The apparatus was essentially the same as that which has been employed by Hinshelwood and his co-workers in a large number of investigations.


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