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- 2. OCH3 NaH Product does not contain P.Electrophilic Addition Soubong neblA-aleid rose 9160910 31 babeen ene singo 14.43 Draw the products formed when each compound is treated with one equivalent of HBr. a. b. C.Which molecules below are anti- aromatic? D A. Structure D Structure B Structure A Structure C B. C. D.
- Synthesis 10.63 Devise a synthesis of each product from the given starting material. More than one step is required. a. b. d. e. Br Br OH OCH3 ta CI OH1. Draw the products of each nucleophilic substitution reaction a. b. D b OH C. d. e. f. Br 1 NaCN + NaOCH3 H₂OO (1) H20, H*; (2) Jones reagent (1) H20, H*; (2) PCC, CH2CI2 (1) conc. H2SO4: (2) Jones reagent O (1) H20, H*; (2) Tollens reagent (1) conc. H2SO4: (2) PCC, CH2CI2 O (1) conc. H2SO4: (2) Tollens reagent
- Help me pleaseThe purine heterocycle occurs commonly in the structure of DNA. a. How is each N atom hybridized? b. In what type of orbital does each lone pair on a N atom reside? c. How many a electrons does purine contain? d. Why is purine aromatic? purineQuestion 1. Draw the product for the following reactions. a. b. C. d. CHO CH3NH₂ NaBH₂CN ai + NH3 NaBH₂CN (CH,CH2)2NH NaBH3CN -NH₂ NaBH3CN