ON THE HALOGEN HYDEIDES AS CONDUCTING SOLVENTS. 

 TABLE I. (continued). 



157 



V 



O.K = * 



ACETAMIDE IN HYDROGEN BROMIDE. 



90-9, 58-8, 23-3, 14-5, 10'2, 6-66, 3-85, 3'03, 2-08, 1-41 

 5-94, 5-88, 6-3, 6-1, 5-8, 6-25, 5-65, 5-45, 4-92, 4-45 



ACETONITRILE IN HYDROGEN BROMIDE. 



33-3, 4-76, 3-70, 2-50, 1-85, 1-47, 1-22, 0-96, 0-72 

 4-61, 5-15, 4-80, 6-2, 6-4, 6-8, G'7, G-7, 7-2 



ETHYL PROPIONATE IN HYDROGEN BROMIDE. 



12-15, 7-14, 5-26, 3-45, 2-63, 1-92, 1-39 

 62, 1-14, 2-00, 1-7, 2-16, 2-30, 2-28 



ORTIIO-NITROTOI.UENE IN HYDROGEN BROMIDE. 



25, 16-6, 12-5, 11-1, 8-33, 3-85, 2-38, 1-50, 0-92, 0-66 



1-00, 1-1G, 0-87, 1-11, 0-92, 0-71, 1-OG, I'OO, 0-94, 0-845 



PIPERIDINE IN SULPHURETTED HYDROGEN. 



9-09, 1-18, 0-90, 0-75, 0-G4, 0-55 

 18, -34, -35, -34, -31, -28 



TETRAETHYLAMMONIUM CHLORIDE IN SULPHURETTED HYDROGEN. 



= 34-5, 11-0, 4-25, 3-32, 2-93 

 = 59-4, 37-G, 16-4, 13-4, 11-3 



