1) Draw the product and mechanism for this transformation. Use electron-movement File Preview se the back if insufficient room. (9 pts). H+ Q= NH2 'N' H - NH 3
Q: The answers are not 1.77E-9 and 1.55E-5. Please help.
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Q: For the first one, I've also tried 1.7E-9 and 1.77E-9. Neither is correct.
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- A B Br FeBr3 1 2 0 =Li then H30* LIAIH4 then H3O* Propose reaction conditions (A) and draw the products (B, C and D) of each transformation. Curved arrow mechanisms are not required.PQ-6. What is the rate determining step of this reaction? CH₂CH3 (A) HOTS H3C (C) NC CH₂CH3 HOTS H3C CH₂CH3 NaCN Hi H3C (S)-isomer (B) OTS acetone Hi H₂C (D) NC CH₂CH3 CO-H Ts CH₂CH3 ∙H H H₂C CO CN H H3C CH₂CH₂ (R)-isomer1. (10 points). Draw a stepwise detailed mechanism for the following reaction showing all the substitution and the elimination products formed. Label the type of the mechanism (SN1, SN2, E1 or E2). Show stereochemistry when applicable. Br CH3CH2OH H₂O 2. (10 points) 0 Br CH3O Na DMSO Draw the detailed mechanism showing ALL possible products formed including stereochemistry and Label mechanism as SN1, SN2, E1 or E2. Show stereochemistry when applicable.
- Cs Scanned with CamScanner 2. Show two reaction schemes to synthesize the following compounds. Pick one reaction scheme and draw the step-by-step reaction mechanism. а. HO-29) Draw all of the expected products for the following reaction. Circle the most dominant product in each reaction. 'BUOK 3 NaOEtDraw the step-by-step reaction mechanism and predict product(s) of the following reaction?
