OH attacks O bonded across DB, then anti OH across DB
Syn addition of OH
Kmno4, COLD
Syn addition of OH
Temperature
Cold adds something, hot takes it off
How to make OH leave
Turn it into a tosylate. Takes off H, puts TS. Uses MEOH to leave
Move DB by adding to DB (Any __________), then _____________ (adding _____)
(Any addn reaction, halides especially), then doing elimination (adding TbuOK)
Use smaller base for ____________ like _____
more sterically hindered area, MeO
Can only use NBS with an _________________
alkane (no double bonds).
MeO can add
methyl group
NaNH2
Joins structures together or makes an alkyne
NaNH3
Takes a bond off
Adds O
t-buok
Does elimination, makes less sterically hindered product
Add base to make a double bond
T-buOK
Making an alkyne
O3, H2o
Adds O=/OH
OH at anti-mark
H2, PD
TAkes bonds off of alkynes
HBr, ROOR
Adds bromine at anti-mark
Addition, elimination over and over
Moves bond
Move ___________, then make them _______
alkenes, alkynes
T-buOK
Makes things leave
Alkane, -ene, -yne is
in alphabetical order