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- 08.20b 1) ВН, THF 2) H,O2, NaOH Modify the given carbon skeleton to draw the major product(s) of the given reaction. If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and Paste to save drawing time. CHComplete the following reactions. Consider stereochemistry to determine if has more than one product. Nal 1.S,2 2. S1 Nal 3. heat Br SH" room temp 5. OTs N, heatWrite the structure(s) for the organic product(s) of the carbohydrate reaction below. ball & stick v|- + labels HOCH2 CH3 0-Ć-CN dilute aq. HCI HO. ČH3 OH Linamarin • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If two diastereomers are formed, draw both. • If no reaction occurs, draw the organic starting material. • Draw carboxylic acids in neutral (unionized) form. • Use “flat" representations of rings, not chairs, in your drawing. Do not draw your answer as a Haworth projection.
- What is(are) the major Organic product(s) in the following reaction? CH; CH; H₂C-C-0-CBr; CBr; CH; H₂C-C-0-CH; CH; CB13 Br3C C 0-CH₂ HBr (SNI) HC CH; H₂C-C-0-H CH, (b) CH; CH; Br CH;Br CH₂OH H;C CH, H₂C C | CH; CH; C CH; (c) H CH + CH₂Br CH; 0—C—CH; -CH:OCH:Organic Chemistry 1 Question. EA24. Please show why the answer is B. letter , and not D. letter . Thank you* 52% 20:08 336551-el... Not saved yet a) Work in pairs. Discuss which of these species could qualify as electrophiles and why. 1. NO2* H,O CH;CO* cr OH- HBr NH3 Br2 b) Can you explain why y not select some of these?
- Give the organic product. dy I. II. OA I D. VV MeO₂C NaOMe CO₂Me CO₂Me P Note: Me= CH3 III. IV. OMe ço,MeFor the substitution reaction. Draw the structure of the intermediate that forms in the rate determining step. Он HBr (aq) Br4. Fill in the missing information (reactants, products, or reagents) in the following transformations. If more than one product is possible, draw structures for all products and indicate the major product. If stereoisomers are possible, draw all isomers, and indicate the major stereoisomer. + a. C. d. e. НО. НО. CI OH OH X PCC NaOCH HBr SOCI J.... CI OH Focus
- f. g. OCH 3 CO₂H OCH 3 pyruvic acid 1. SOCI22 2.? NaBH4 CH3OH methicillin (narrow-spectrum, B-lactam antibiotic)? H₂SO4 (cat) C6H8O4 (show structure)NH, CH31(excess) aq. Na2CO3 →A A48 "A".... NH, CH3 NH, CH, H,C (1) (2) CH3 CH, NH2 JA) Ph-N(CH) (3) CH, CH35. Classify the following reagents as either nucleophiles or electrophiles: Zn? CH;NH, , HS , OH; , CH;COOH , H,SO,