оо 15. HỌN _C02 1) (CH3)3COCOCOC(CH3)3 Ph 2) -N: C: NH- CHO HO+H PhNHNH | 16. H+OH (3 equiv.) н+он HOHH CH2OH 17. Use ANY needed reagents to effect the following transformation. (30 points) Br ÇO2Et ON starting material product
CHO HO EH PhNHNH | 16. нон (3 equiv.) НО H H -ОН CH2OH
оо 15. H2N CO2 1) (CH3)3COCOCOC(CH3)3 아 2) -N:CENA CHO HO+H PhNHNH | 16. H -OH (3 equiv.) HO -H H- CH2OH -OH
draw the structure for the major organic product of each of the following reactions. HOTH PHNHNH, 16. CHO HOH (3 equiv.) H-OH HO+H CHOH
PhNHNH | 16. CHO HO FH H+OH (3 equiv.) НОН HO FH CH2OH 17. Use ANY needed reagents to effect the following transformation. (30 points) ÇO2Et O ON starting material product
оо 15. H-N co;" 1) (CH3),coċOCOC(CH3)3 2) -N: C:NH- CHO HOEH PhNHNH | 16. н+он (3 equiv.) HO+H н+он CH2OH
оо 15. H-N co;" 1) (CH3),coċOCOC(CH3)3 2) -N: C:NH- CHO HOEH PhNHNH | 16. н+он (3 equiv.) HO+H н+он CH2OH
LP HH4 Pn PhPh. P Ph Ph Ph Fig. 4 shield Case stu -5,0 8/ppm uffield and O PPh.. A shift to more positive 8 (higher frequency) generally accompanies the "P NMR spectrum of a phosphane before use in the laboratory is an easy way of checking din air. Case st The 31 Self-study exercise hedral tent w centra es of Hg (equal al for Hg is com- Hg couple with wo doublets. h of the doublets plitting is called...
draw the structure for the major organic product of each of the following reactions. PhNHNH | 16. CHO Нон н+он (3 equiv.) нон но-н CH2OH
i think its D please show work typach Ph H Ph H Ph Ph H H Ph