1/6
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced |
---|
No study sessions yet.
cyclic acetal formation attacks from
Nu- attack
how to make cyclic acetal
diol —> most reactive C=O group
why is cyclic acetals more favorable
entropically neutral
cyclic acetals cannot be attacked from
Grignard and hydride reagents
show thioacetal formation
show Raney Nickel
what is a good way of removing the C=O group all together
create thioacetal and then do Raney Nickel