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Organic Chemistry 2 Lecture notes 9
Organic Chemistry II (AS.030.206.)
Johns Hopkins University
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Organic Chemistry Lecture 8-rest (Johns Hopkins)Preview text
DCC HO in proteins protein, i protone DMAP DMSO great solvent immisable o ii dissolves many organic mdecles Ester Hydrolysis: cevere of Fischer Statification effer rist me sion K2O Line we no me (x5) isopropyl benzoate beneat acid isopropand Drive reaction right Transecherification: TI (sodium Metroide) me (Ethand) EtoNa eton Ph for oct MB injist Eister Methyl EHO Saparification Base Promoted Ester Hydrolysis (Making Soop) girl of me NaOH H2O Ph fate OH milo depositphote OH 8 me and O No ODH D glycerd esters minim head glycerd backbone mumic k SOAP KOH(L(ye) H2 spectator mumical s ion Transesterifications a B Carbon position Isopropyl cirnamete me Blow DEL o methory group 8 GIOH Ph me Ph of Ph Mast veryly group enols RI 400 o 6 540 H Ph off ph OCt regove EXOM very EN density probante pulled towards it smaking wingl more Arumatic Rings Diazonium lon Intermediate N NH2 110 (Sodium Minise) N NaNo2 HBFy(acid) high energy Aniline diazonium ion reaction happens unstable I Weckrophiled R Rapes me Taulfer NEO M2 I protonals Ph strong acid mere strong BOLG acid NH2 for OH OF off! N Has N every reactive! 1 A N2 BF40 that e OH2 of Ph CH2Cl2 Ph phenyl diazonium ion cation NH2 I 11 flowine Amine group to group Many ways to transform aniline into derivatized aromatic systems with diazetneum ion intermediates Ar EAS can react of nucleaphiles (another reaction way 0 that and DCC HO in proteins protein, i protone DMAP DMSO great solvent immisable o ii dissolves many organic mdecles Ester Hydrolysis: cevere of Fischer Statification effer rist me sion K2O Line we no me (x5) isopropyl benzoate beneat acid isopropand Drive reaction right Transecherification: TI (sodium Metroide) me (Ethand) EtoNa eton Ph for oct MB injist Eister Methyl EHO Saparification Base Promoted Ester Hydrolysis (Making Soop) girl of me NaOH H2O Ph fate OH milo depositphote OH 8 me and O No ODH D glycerd esters minim head glycerd backbone mumic k SOAP KOH(L(ye) H2 spectator mumical s ion Transesterifications a B Carbon position Isopropyl cirnamete me Blow DEL o methory group 8 GIOH Ph me Ph of Ph Mast veryly group enols RI 400 o 6 540 H Ph off ph OCt regove EXOM very EN density probante pulled towards it smaking wingl more Arumatic Rings Diazonium lon Intermediate N NH2 110 (Sodium Minise) N NaNo2 HBFy(acid) high energy Aniline diazonium ion reaction happens unstable I Weckrophiled R Rapes me Taulfer NEO M2 I protonals Ph strong acid mere strong BOLG acid NH2 for OH OF off! N Has N every reactive! 1 A N2 BF40 that e OH2 of Ph CH2Cl2 Ph phenyl diazonium ion cation NH2 I 11 flowine Amine group to group Many ways to transform aniline into derivatized aromatic systems with diazetneum ion intermediates Ar EAS can react of nucleaphiles (another reaction way 0 that and
Organic Chemistry 2 Lecture notes 9
Course: Organic Chemistry II (AS.030.206.)
University: Johns Hopkins University
