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Summary of organic chemistry class
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· Amine,itsacids (^) (NHattention amine up H^ down Ethane^ -^ Cats^ GpHac Decure
primary amine / From the or Propane -^ alo Ex:Ethanol R-OH-^ its^ C/OH^
Butane-CyH,"" is Underne i Penture^ -^ CSH,z CirHastDodecane · (^) Thiol
(6H,p 43Hs- Tridesame
ins^ at^ OH^ Heptane^ ->^ GHis^ up GottyIcosan
=Hodot^
added to^ natural Octure^ to^ [8Hig^ (soHt62-Triacontane gas for^ leak^ detection^ be^ methane^ is^ odorless sesion --/^ OH · Alkyl halide^ Chaloalkane)^ ->^ R^
-> (^) sel us (^) refrigerants in aerosols H dy (^) channing etc^ but^ notused^ anymore^ by^ any halogen allaveo double bond ->^ --^ ↑Ou theydamagemoneta
allyne: triple^ bodiesinacoins down^ OH H H isomer +H^ H
Diestovermers **y= OH
H
-> general anesthetic -^ ,^ - frust CHS^ CH3^ CH3^ CH · Epoxide
h -> especialtypeofagalie XxxCA et sense -> Ree - Ex: Epoxy
Ex:Cinnamedelye ->, (^) *t contains (^) Editybols (^) must stable equatorial -> (^) smell of Cinnamon carbony.Is↓ has iton^ one n side^5 carbon · R^ alygrap Ketone (^) aldehyde
EX: (^) Aceture (^) igegen -> Commonly used (^) solvent - - isocy (ncerre)
H cool tys out -=+ Br tericrepe Vinegar bio^ +BU · (^) Ester ->^ esters ⑲ S · (^) e rude from (^) abrhals (^) arboxylic acids shelle (condensation^ reactionin^ ->^ there^ I^ -
with carbon containinggroup -^ so take offacidic^ proton +Bu · (^) Amides Ra
bundbutactualer; Peterre^ - stevic repulsion blu^ a is barrier to rotation of In (^) only this case eRieterhydrogen or carbon neighboringfert-butyl^ groups
funaldecle ketehere also unfavorable^ gauche internations blu (^) tert-butyl groups as^ t^ pa^ HiHe^ lower every equatorial -
is set H Ecl Hy-CE l ⑬ -amer is
(A
sp -
⑰ (^) ③ (^) o = 0 ②
electronegativity MRIor^ X^ ut
bouding HO (^) b ·t CH OH antiboding bitedbe e ASBtDis ASCesame^ BEC- (^) Dias curban centers Oxygen is^ more ebchowerin^ e it (^) bonding orbital- polarized towels oxygen ↑ antibonding- opposite -^ lobes or carbon one (^) bigger