Solution=
In the first step sodium
methoxide take proton from nitromethane. Then Michael addition take
place i.e.; 1,4 addition. H2 Pd/c reduces the nitro
group to NH2 group, then H2O is removed and
pyrrolidine is formed.
Propose a synthesis. Intermediate is appreciate
4) Propose a synthesis. cu HN
1) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. Lfcce HN 2) Propose a synthesis. OH 3) Propose a synthesis. Ph OH 1) PCC 2) 3)acid work up 4)2 NH 5) O3, 6) DMS 7)? 8)? 9) H2/Ni 4) Propose a synthesis. HN 5) Name the following using IUPAC nomenclature. Br
1) Propose a synthesis of the following 2) Propose a synthesis. HOL 3) Propose a synthesis. 4) Provide the structure of the polyamide formed in this reaction. H2O) Polyamide Heat 5) Propose a synthesis. 2 / OH
4. Propose a synthesis for the following. glied Lot
4) Propose a synthesis. ད་དབང་བཟང་བས ། –
Help please, thank you.
1) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use HN.
Propose a synthesis, accounting for all reagents and steps, of
the following peptide. Include a mechanism for the formation of
each intermediate (if a step is repeated, the mechanism only needs
to be shown once; no mechanism is expected for catalytic
hydrogenation – if used).
HN HINN Li Low ZI
starting with benzene, propose a reasonable synthesis of the
following compound.
propose a reasonable synthesis of the following compound. NO2
Propose a synthesis. Intermediate is appreciate
3) Propose a synthesis. T ph 1) PCC OH NH 2) 3)acid work up 4) ? 5) 03, 6) DMS 7)? 8)? 9) H/Ni
Propose a synthesis
5. Propose a synthesis B OH OEt OE K OB