less - Answers the more s character a carbocation has, the _____stable it is
the same as - Answers when looking at an epoxide, the orientation around the oxygen is _________ the
orientation around the double bond in the reactant
BrOH - Answers when added with base makes an epoxide
Br2 - Answers adds 2 Brs in anti conformation
lindlar catalyst - Answers produces a Z alkene from an alkyne (adds 2 Hs in syn)
add more electronegative atom, add pi bond - Answers 2 ways of producing an oxidation reaction
remove electronegative atom, remove pi bond - Answers 2 ways of producing a reduction reaction
HBr - Answers when this reaction occurs there is a scrambling of dashes and wedges (not just anti or syn,
no fixed relationship)
triple bond (base) reaction - Answers when the product has more carbons than the reactant, this
reaction is needed
radical halogenation - Answers when the reactant only has carbons and hydrogens, this reaction will
occur first
O3/Zn or OsO4/NMO/HIO4 - Answers when the product has less carbons than the reactant, one of these
reaction is needed
O3/Zn and OsO4/NMO/HIO4 - Answers these two reactions cleaves c-c bonds
elimination - Answers when forming a double bond, this reaction is needed
Li/NH3 - Answers creates an E alkene from an alkyne (adds 2 Hs anti)
ozonolysis - Answers cuts through double bonds and adds oxygen to them
less, more - Answers the lower the BDE for H-X*, the ______ reactive X* is, and the ______ selective X*
is
less, more - Answers in an X-OH reaction, the X bonds to the _____ substituted carbon and the OH
bonds to the _____ substituted carbon
H2 - Answers this reacts with triple and double bonds to form hydrocarbon chains in hydrogenation
reactions
carbon next to double bond - Answers allylic position is