a "the oxime and the nitrile of the “Gluetede (both pe the corres 
-- m. p. 192° was obtained. The sen nee did or — in the | te 
The 4 Baton of eanipheniiidene: 6 acetaldehytie ith zinc sid lian 
on warming (Clemmenssen’ S method) yielded ermetivleas pea (b- Pe 178° 
resulted on treating with hydrobromic acid gas, sae: ere ‘resulted 2 bromo 
camphane (IX), (b. p. 108 to 110° at 17 mm; dase 1. 175), Rigger oe Maree Ss 
but ne sodium bisulphite sompeiiel i | 
Finally, the aldehyde and the Lene. eee -ally compounds further 
. 
cyclic double bond remained whilst the othes was broken. Two aldehydes were aa U 
as reaction products (e. g. CoHis: CH- vers and HCHO) EO a ee ee 
CHy- CH : ¢ = (CH,)s CHom : : SE (Chis) CH; 
7 CHy | CHe Seth any ih ete 
CH, CH cH, ce CH CoH oe CH. ee 
-* () Camphenilane. (II) Camphenilene (Radicle). (Ill) Campheniliden 
a Formula according to Langlois. _ Formula ee ok 
Rae CHa CH C= (CH, Cie -CH COACH 
Shy | « mt raat es 
7 - , F } | 
BCH -CHe-C= Ch, | Ch CH C0 
s - (IV) Camphene. ; | (V) Camphenitone. 
i ‘ 4) Cf. Report October 1907, 139. ; ; ! f tee es 
