TABLE SHOWING SOME OF THE PRODUCTS WHICH MAY BE DERIVED FROM ALCOHOL. 



+ 2 



2 H 5 . HO 

 alcohol 



+ 



CH..COOH 



acetic acid 

 + CH3.COOH I +H.COOH 



+ NH 3 



CH 3 .CHO + H a O 

 aldehyde 



I +HCN 



CO.(CH 3 ) 2 + H 2 C0 3 

 acetone 



+ HCN 



dimethyl ketone 

 cyanhydrin 



CH 3 .CHO + H 2 C0 3 



aldehyde 



CH, 



CHOH . NH 2 

 e ammonia 



I'll. (Ml. 



condensed 



C 3 H 7 drCHO 



aldol 



or 



C 3 H 5 .CHO + H 2 



crotonic aldehyde 



1 ±*_, 



2CO„ + 2H 2 



CH. 



+ HON I 



,CHJg*p+H 2 

 ethidene cyanamide 



+ col NH = I 



+ ^ u (OC 2 H 5 I + 2H.0 



+ NH 3 



CH 3 .CH. 



(NH a 

 "JCN 

 ethidene cyanamide 



+ 2H 2 I + C0jgg|j 5 



'HO 



)CN | 

 ethidene cyanhydrin 

 I +2H a 



Oil, 

 1 0, 



CH ^ 0H 

 Ln " ICOOH 

 lactic- aoid 



Nll 3 



I B « 



C 2Hj |NH.CO N H 2orC2H3 



+ 2H„0 



(nh 2 ){ 



CONH, 



CN 



- HO . C 2 H 



C 2 H 3 (NH 2 )|™ 2 + NH 



asparagme 

 fermented | 



+ 4 



+ O 



+ 1 + 4H 2 



O bO 



e= P 



5 s o 



B o 



2. O 



I i 



NHs +NH 3 



COOH 

 alanine 

 transformed it becomes 

 ]NH„ 

 10C 2 H 3 

 ethylic carbamate 

 or nrethane 

 3HCN + 3molec. I + NH, 



C 2 H a (01I) 2 + 00 3 - 

 oxalic acid 



ll,c> 



CH 3 .CH- 



CO 



3C 2 H, . HO + C 6 H,N 4 0, + CN . NH 2 

 alcohol uric acid cyanamide 



CO |^ + C 2 H 5 .0H 

 urea alcohol 



+ 



CH..COOH I- I1.000H 

 aoetio aoid formio aoid 



OH 8 .CHO + CO,+H,0 

 aldehyde 



I To I'm a page 200. 





