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17 Cards in this Set

  • Front
  • Back

why cant halogenation in ___ create cis configuration?

stereochemistry, because there is a shield so it can only come from the opposing side

the outside chemical is usually the ____phile

nucleophile

electrons always get pulled by more ____

electronegative

when adding halohydrins you get something and

hydronium

when adding hydrogen through ___ and ___ we always get __ configuration

palldium, platinum, cis

ozone reactions are pretty much

cutting it up at double bond and making a carbonyl group at each end (double bond)



conjugated diene

bond that alternate with single bonds

alkynes are ___ reactive than alkenes

less

e--> z-->

trans cis

toluene


phenol


aniline


acetophenone


benzaldehyde


benzoic acid


ortho-Xylene


styrene

benzyle

arenes

less than 7 are benzene otherwise its the parent chain

nitric acid turns into nitronium ion

NO2OH NO2

sulfur trioxide

s double bond o double bond o and single bond O

adding alkyl and acyl(carbonyl group) name

friedel crafts

carbonyl push substituents

meta

hydryl push it

order and para