Table III KBr and KC1.
c = -0-0001488.
 | A table should appear at this position in the text. See Help:Table for formatting instructions. |
7-0 6-9
25ft -5
277-2
270-9
-9370
8-0
272 -6*
291 -5*
-9351
9-0
9-1
2S5-5
305-5
305-9
-9331
10-0
10-0
297-8
319-7
319-7
0-9313
11 -0
10-9
310-5
334-1
334-0
'9294
12-0
323 -0*
348 -2*
-9276
13-0
12 -9 335 -5
362-5
362-4
0-9257
14-0
13-85
347-7
377-1
376-2
-9239
Table IV. CdBr 2 . 4H 2 and KN0 3 .
c = 0-00148.
o
4-2
4-0
274 -0 289 -5
288 -6 -9494
4-6
278 -0* 291 -4*
-9553
5-8
6-0
288 -0 296 -0
296 -8 9701
6-6
6-87
293 -0 298 -7
299 -7 -9775
7-0
7-8
298-0 302-0
3U2 -5 -9849
8-7
303 -0* 305 -3*
-9924
10-0
9-61
308 -0 309 -3
308 -0 -9998
11-4 10-60
313-0
313-U
310-8 1 -007
The very satisfactory agreement found in the case of the above salts is of interest from the fact that the two substances are ionised in a very different degree.
Table V. m- and ^;-Oxybenzoic Acids. c = 0-00104.
0-088
-0868
286 8
300-0
300-7
-9537
0-096
-0976
2887
301 7 302 -1
-9556
0-108
291-5*
304 -1*
-95-S6
0-116
0-114
293 -2
305 -6 305 -3
9603
0-124
0-124
205 -1
306 -6
306 6
-9623
0-136
0-1396
297-5
308-0
308-3
0-9648
0-148
-1528
299-5
309-2
309-7
-9669
0-172
0-1756
303-1
311-8
312-2
-9706
0-190
305 -0*
313 -6*
-9726
0-210
0-202
307
316-0
315-0
-9746
0-220
0-206
307 -9
317-1
315-6
-9756
0-240
-2156
309-8
318-9
316-9
-9775
The preceding examples are only a few of the cases in which I have tested the validity of the relationship above stated, and, as can be seen, the agreement between theory and experiment is very satis-
