RelativeResourceManager (2)

RelativeResourceManager (2) - b. Will the reactions favour...

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Sample midterm CHM2120A 2010 1. Name or draw the structure of the following molecules, as appropriate. a. ( E ) isopropyl 4-hydroxy-4-methylpent-2-enoate b. OH H 3 CO 2. a. Identify whether each of the following molecules is aromatic, anti-aromatic, or non- aromatic. b. Justify your response. i. H N
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ii. 3. Give the major organic product of each of the following reactions. Ph Cl HOCH 3 (solvent) NaOCH 3 O 1. KCN 2. H 3 O + OH 1. ClSO 2 CH 3 , weak base 2. NaNHCH 3 OsO 4 , NMO
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4. a. Draw the mechanism and products for the following reactions.
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Unformatted text preview: b. Will the reactions favour starting materials or products? c. Justify your choices in part b. NH NH 2 HO Na H + NH 3 HO + Cl S Na 5. Circle the most basic atom in imidazole and explain your choice. N N H 6. Use orbital to show why backside attack occurs in S N 2 reactions and why the proton and leaving group must be antiperiplanar in an E2 reaction....
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RelativeResourceManager (2) - b. Will the reactions favour...

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