CHM 2310-001; PDQ 12 2. Propose a mechanism for the following transformation. Be sure to account...
CHM 2310-001 (HLS); PDQ 2 Apply what you know about resonance to acid/base chemistry. Show all relevant resonance structures and the curved arrows that shows interconversion of structures. Which base is most stable = weakest base? How do you know?
Propose a reasonable mechanism for the following transformation. Be sure to include lone pairs, curved arrows, and all formal charges. Draw your mechanism on a piece of paper for tablet), then upload a scan or photo of your answer. HN (excess)
1) Propose a mechanism for the following two-step transformation. Be sure to include all curved arrows, intermediates, and by-products. (5 marks) Br -OH Br 1) NaOH, HÀO 2) HBO ОН
1) Propose a mechanism for the following two-step transformation. Be sure to include all curved arrows, intermediates, and by-products. (5 marks) Br -OH 1) NaOH, HO 2) HBO Br OH 2) Propose a synthesis for the transformation below. You may use any reagent discussed in the course notes or textbook, as well as any additional compound with 2 or fewer C atoms in your solution. (5 marks) هر
propose a mechanism that shows the following transformation,
find your electrophile and nucleophile
Propose a mechanism that shows the following transformation (Hint: find your electrophile and nucleophile) al do a SO CI + No H
7. Provide a detailed me rovide a detailed mechanism for the following transformation. Be sure to use curved arrows, Show all relevant lone pairs and bonds, formal charges and all intermediates. Be sure to account for the appropriate stereochemistry. (5 points) NaH (1 equiv), THF Me Me
Propose a plausible mechanism for the following transformation: H2SO4 Propose an efficient synthesis for each of the following transformations:
7. Propose a mechanism for the following transformation: Å Ho 8. Propose a plausible mechanism for the following isomerization and explain why the equilibrium favors the product. OH 9. Cinnamaldehyde is one of the primary components of cinnamon oil. Propose TWO separate syntheses of cinnamaldehyde from benzene and any organic material with less than three carbons cinnamaldehyde
Propose a plausible mechanism for the following transformation. For the mechanism, draw the curved arrows as needed. Include lone pairs and cl 1) NaOH 2) H20* OH HO
Question 2 Propose a plausible mechanism for the following transformation. For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do not use abbreviations such as Me or Ph. OH