Reaction Summary
Thiol synthesis via SN2 with sodium hydrosulfide
a)
Alcohol synthesis via SN2 with hydroxide
b)
Acid hydrolysis of an alkene
c)
Markovnikov alcohol
Markovnikov Oxymercuration/Demercuration of an alkene in water
d)
Markovnikov alcohol
Anti-Markovnikov hydroboration of an alkene
e)
Anti-Markovnikov alcohol
Syn-dihydroxylation of an alkene using osmium tetroxide
f)
cis glycol
Syn-dihydroxylation of an alkene using potassium permanganate
g)
cis glycol
Epoxidation of an alkene followed by acid hydrolysis
h)
trans glycol
Acetylide attack of an epoxide
i)
Acetylide attack of a carbonyl
j)
Synthesis of a Grignard reagent
k)
Synthesis of organolithium reagent
l)
Grignard reagent attacks of carbonyls
m)
n)
o)
p)
q)
Grignard attack of epoxides
r)
Synthesis of a Gilman reagent
s)
Gilman reagent with alkyl halide
t)
Reductions of carbonyls
u)
v)
w)
x)
y)
z)
