Question 20 Predict the expected product for each reaction and provide IUPAC name for the correct starting material to yield the desired epoxide: 1 2 MCPBA NAME ů 1. CH3CH2MgBr ? 2. H₂O A B OH Box 1 (name): Box 2: OH C D OH OH
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- Complete the given reactions by drawing the structures of the major organic products: Please draw the completed reaction OH HO HOCN H₂N H₂O H3PO4 OH HO HO. (excess) H3O+ H2SO4 H*Aa 43.Determine the reagents required for the following syntheses. More than one reaction is likely required. a) b) c) d) OH OH olm NH₂ MeO NHMe Me. Me OH OH
- Question 18 Predict the expected product for each reaction and name the correct starting material to yield the desired epoxide: 1 R 2 O-OH 1. NaCN NAME 2. H₂O ? A B CN OH OH CN Box 1 (name): Box 2: с CN ... OH D OH ... CNWhich of the following reactions does not proceed? O Dehydration of 2-propanol with H;SO, catalyst Hydrogenation of benzene with H2/Pt o Oxidation of 2-propanol by H,Cro O Hydrobromination of 2-butene with HBr O Hydration of cyclohexene with H2O/H2SO4Please include the names for products A and B, thanks!
- Draw the structure of the products formed in the following reactions. a) CN H,0, H* CH3 он b) H3C- -CI + CH3 c) CH3 KMNO4, A, H,O" CH3 d) Br Mg, éther CO, H*QUESTION 27 In the synthesis of 2-methyl-pentan-2-ol from pentan-2-one, the source of the nucleophile in nucleophilic attack on the carbonyl carbon is O C=N O CH3MgBr O -C=CCH3 O NAOCH3 O KMNO4 QUESTION 28 Resonance stabilization can stabilize O methyl O primary O secondary O tertiary O benzylic carbocations.Number 6 please