b. CH3 H3C CH3 CH3 H3C an unexpected product, containing a single 9- membered ring the expected product, containing two fused rings H3C-I (H3C)2CuLi an enolate
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- 5. Conjugate vs Direct Addition Draw the major organic product formed for each reaction. (a) (b) i NaSCH3 HSCH3 H3C LiAlH4 then H₂O 6. Reactions of Enolates (- (a) (b) (CH3)2CuLi H3C then H3C H3C. KOtBuA) what is the major product if E2 mechanism is followed in the reaction (A-D) B) what is the complete mechanism with steps to form the major productIn each reaction box, place the best reagent and conditions from the list below.
- Identify compounds A – E of the reaction sequence shown in Scheme III, making sure to include stereochemistry as appropriate.a) Identify compound A in Scheme III. b) Identify compound B in Scheme III. c) Identify compound C in Scheme III. d) Identify compound D in Scheme III. e) Identify compound E in Scheme III.identify the viable synthetic plan for the conversion of A to B.Please provide the reagent (A) and the product (B) of the following scheme. A H3O* HO. Eto. EtO. H. B A HO. А: LIAIH4, B: HO. A: LIAIH4, B: HO, А: NaBH4, B: HO. А: NaBH4, B:
- Provide a 3-5 step synthetic route the target molecule from starting material A. Be sure to account for relative stereochemistry and to suggest reagents/conditions for each step CN .CI H3C CN Target molecule starting material (A)Which alkene gives a meso compound upon reaction with bromine (Br2)? а. O b. d.13
- Please explain, thank you:)Q12. (1-bromoethyl)benzene 1 udergoes an elimination following an E1 mechanism. Fill in the following synthetic scheme by drawing the structure of intermediate 2 and product 3. The chemical formula of product 3 is provided as guidance. CH; RDS Br C3Hg E1 2 3Draw the product of each asymmetric epoxidation reaction.