H2SO4, H2O, HgSO4
OH at mark, then O
H3O+, H2O
DB steals H on H3O+ , creating + tert carbon. Resonance forms Ketone (O=<) and H3O+
BH3, TFH, H2O2, NaOH
Gets rid of 3x bond, O= at mark
O=/OH added to both
O=/OH added to R, C has 2x O=
Alkylation of terminal acetylides, starting with terminal acetyline
NH2 takes an H off, E- take R from R-X. Can be done 2x to replace both H with R
Radicals are > stable with
Bulkier structures
KOT
HOT
Takes Br off, makes DB