H2O COH + RNH2 H+ or O HO- COH on on КОН N-H + R-X N-R Ο RNH2 aq. H2NNH2 ΝΗ Why can this reaction not be used to form 2...
H2O COH + RNH2 H+ or O HO- COH on on КОН N-H + R-X N-R Ο RNH2 aq. H2NNH2 ΝΗ Why can this reaction not be used to form 2 or 3 amines? Draw a reasonable mechanism for the hydrolysis (acidic or basic) and the Ing- Manske procedure.
provide a mechanism for both of the reactions provided. why can secondary or tertiary amines not be formed using this reaction? 1. Complete a mechanism for both pathways below, the hydrolysis (use acidic or basic conditions - note which is used) and the Ing- Manske procedure. Provide intermediates with arrows for each step. H2O .COH + RNH2 Hoor HO "co₂H oa aq. H2NNH2 2. Why can this reaction only form 1 (primary) amines, not 2 (secondary) or 3 (tertiary)?
2. A reaction discussed in class involved treating a primary amine with chloroform under basic! conditions to form an isocyanide. When a secondary amine was used instead, an amide was formed: NaOH NaOH CHCIE R-NEC + CHCIE RNH2 + Lº amine RỌNH 2° amine HANR2 2. A reaction discussed in class involved treating a primary amine with chloroform under basic conditions to form an isocyanide. When a secondary amine was used instead, an amide was formed: NaOH NaOH CHCIE R-NEC...
CHO 1. NH2OH 2. Ac2o 3. CH,O CHO OH H- HO H HO H HCN H OH OH H- OH H- -OH H- CH2OH CH2OH The Wohl degradation is a series of reactions that shorten an aldose chain by one carbon, it is almost the exact opposite of the Kiliani In this reaction the aldose aldehyde carbonyl group is converted into a nitrile. The resulting cyanohydrin loses HCN under basic cone Conversion of the aldehyde to a nitrile is accomplished...