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- mechanism: El CI CH3NH₂ A Heat elimination(CH3)₂CHCH₂OC=OCH₂CH₂ H₂SO4 H₂OE0. 27. Draw sheieolsonteis of ehtral and achiral structures. (a) Braw the enantionter of the struchire shown. It the structure has ho enantiomer, leave blank, (b) braw a thastereomer of the strictive shown. If the structure has no dlastereomers, leave blank:
- Which of the following disaccharides is a non-reducing sugar? НО O U О О НО- O A D B لیتا ОН ОН НО- ОН НО. ОН ОН A C НО НО ОН ОН ОН ОН прион HO OH но.... HO НО -ОН HO ОН в NH₂ OH то OH D II O -OH НО OH NH₂ OHCH₂CH₂CCH₂CH₂CH, H₂O Br₂ tert-BUO CH₂CH₂CH₂CH₂Br CHỊCH C—CH CHỊCH; CH₂CH₂CH₂CH.Br CH₂CH3 tert-BuO CH₂CH₂CH=CH₂ H₂O NaNH, CH3CH₂Br -CH₂CH₂CHCH₂ CH;CH C=CCHỊCH, Br excess H₂SO4 Re H₂SO4 CH;CH,C=CH CHỊCH C=CDraw the following monosaccharides, using chair conformations for the pyranoses andHaworth projections for the furanoses.(a) a-d-mannopyranose (C2 epimer of glucose)
- * Antimalarial (chloroquine) Hote CI HN The molecule is acidic @ Number of. location of chival 3 is the 47 The Name chiral centre. centre or molecule basic and The optical active? of Heterocyclic ring present?Draw the product of the mutarotation of the monosaccharide shown below. ОН CH₂OH ОН ОН H3O+ ОН of вPescribe what the purpose of ma King_a "derivative" like a semicarbizides, phenyhydrazin DNP solid. How is this helplul ur unknowns(s). your