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hydrohalogenation
H-X ex. H-Br
has carbocation intermediate
what does adding ROOR (peroxide) do in hydrohalogenation?
makes it anti markovinikov, halogen on least substituted side
acid catalyzed hydration
diluted acid like h30 or h2so4?
has carbocation intermediate
follows markovinikov
oxymercuration-demercuration
Hg(oac0)2 h20
NaBh4
follows markovinokov
is anti stereoselectivity
hydroboration oxidation
BH3 , THF
H2o2, naoh
is anti markovinikov
stereoselectivity is syn
catalytic hydrogenation
H2
metal catalyst like pd, pt, ni
is syn addition
exothermic reaction
halogenation
just halogen ex, br2, cl2
anti stereoselectivity
halohydrin
halogen + water or alcohol
is anti markovinikov and anti stereoselectivity
anti-dihydroxylation
treated with aproxy acid (RCO3H)
makes a epoxide
adds two OH that are anti stereoselectivity
syn-dihydroxylation
Oso4
Nahso3
or
Kmno4 (cold diluted)
Naoh
adds two OH with syn stereoselectivity
oxidative cleavage
used ozone or kmno4 but under (hot and concentrated conditions)
makes ketones and aldehydes
split double bond and had in two oxygens on both sides
what happens when ur doing a acid catalyzed reaction and add concentrated acid instead of dilute?
favours formation of OH —> Alkene
using diluted does alkene to an OH.