2. Identify and show the asymmetric carbon in the given structures? (4 Marks) CI CH2OH otonon as a d 3. How would you ra
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2. Identify and show the asymmetric carbon in the given structures? (4 Marks) CI CH2OH otonon as a d 3. How would you ra
2. Identify and show the asymmetric carbon in the given structures? (4 Marks) CI CH2OH otonon as a d 3. How would you rank substituents in the given compounds in order of higher priority using Cahn Ingold Prelog rules/nomenclature. (2 Marks) CO2H Br HO-C-OCH 1-C-F CO2CH3 CI 1 1 4. Assign R and S configuration. Write each step. (2 Marks) H OH ночі Н. Br он a b 5. Assign E and Z configuration and write complete IUPAC names for the given compounds. (2 Marks) Br CI H b a 6. The electrophilic addition of HBr to 2-methylpropene is regiospecific. Which product is formed and why? (2 Marks) H2C H HBr H2C H