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Mechanism of this reaction please!
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- 6829Cu->0-1beta+?H H-C-OH HO-C-H H²-OH H-C-OH 6 CH₂-OH D-(+)-glucose rotate H 6 5 C-CH₂-OH HI OH OH I OH C H 21 OH H H CH₂-OH -OH OH H H OH = H OH CH₂-OH 5 H OH H H ß (a) OH (H) H (OH) OH anomeric carbon D-glucopyranose 1. Redraw wrapping from C1-C6 clockwise. Keep all things on the right of the Fisher projection pointing down, all things on the left pointing up.O H OTS KCN CHy CN
- Predict the B-elimination product formed when each chloroalkane is treated with sodium ethoxide in ethanol. If two or more products might be formed, draw only the major product. (a) • All hydrogen atoms are implied. • Apply formal charges where appropriate. • Omit lone pairs and radical electrons from your answer. ITAYY Cl #[ ] در • Sn Ⓡ Previous NextH. N- imert) waib)omoatosib owl to erit waib) aemoaloanate ow io H H 12 ( k) CH;NHCH,OCH;CONHCH3 houulifanoo yam as wsid (e1eoet lenonulanos o) leulocR en H. H. c=Ć-C- H. нно о H. онн rplugelomiclinos ns bas lSo 0 H. нн H. H. H H- H-Ć H HNH N H -H H. H. (! H H. H---H H H H. H H H-C-C-C=C-C-C-H HHH H---S-5-5--H H H f) (CH3CH2O)2CO CH3COCH2CO2CH3 b) CH;CHBr(CH2)¿CH(CH3)2 a) CH3(CH2)3CH3 CH3CHCHCH2CHCH2 (CH3)3CCH2CH3 STEREOCHEMISTRY 1. Convert the following condensed and Lewis structures into line-angle structuresN-NHPH CHO CH2OH H- C=N-NHPH Но- -H- 3 equiv Но- -H- 3 equiv Но- PHNHNH2 PHNHNH, H- H- OH H- -O- H- H- -HO- H- -HO- ČH2OH ČH2OH ČH2OH D-glucose osazone D-fructose + NH3 + PHNH2 + 2 H20 The final step in the formation of the osazone from glucose is the reaction of the keto imine with 2 equivalents of phenylhydrazine to yield the osazone plus ammonia. This reaction involves the following intermediate steps: 1. Addition of phenylhydrazine to the imine and proton transfer to yield intermediate 1; 2. Elimination of ammonia to yield phenylhydrazone 2; 3. Addition of phenylhydrazine to the ketone to yield tetrahedral intermediate 3; 4. Proton transfer yields carbinolamine 4; 5. Elimination of water yields the final product osazone. Write out the mechanism on a separate sh of paper and then draw the structure of tetrahedral intermediate 3. NH НО- -H H- -ОН H- -ОН ОН Glucose keto imine Previous Ne