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Dehydrohalogenation
elimination of HX from alkyl halide using heat and KOH
May create racemic mixture
dehydration
elimination of H-OH from an alcohol, requires a strong acid
Why can hydrohalogenations make racemic mixtures?
Because the carbocation is flat, and can be attacked from either side, So if chiral C, both R and S products will be made.
Substrates
main organic component reacting
(here it’s an alkene)
Reagents -
what reacting substrate with
Products -
what product (s) do you get?