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- Please identify priorities of functional groups and name following molecules based on thier stereochemistry as R or SFor the given ee values, calculate the percentage of each enantiomer present. Q: 90% ee1-methylcyclohexene is reacted with the following reactants. Write products. Write which stereochemistry is valid (syn/anti, racemization, antimarkovnikof, etc). 1- Br2/ H2O 2- CH2N2/heat
- Predict mechanistically what stereoisomers of 3-chloro-5-methylcyclohexene should form when (image below) is treated with Lucas reagent (ZnCl2/H30+Cl-).Is the following alkene E,Z, or neither? a. E b. Z c. neither d. It is one or the other, but which is impossible to determine from the information givenIdentify the stereochemistry of the indicated carbon, write R or S 6. 7. 8. 9. 10.
- Which compound is more stable: cis-1,2-dimethylcyclopropane or trans-1,2- dimethylcyclopropane? Explain your answer. Thank you.Which of the following substituents acts as a moderate activator and ortho/para director? -SO3H -Br -NHCOR -COOH -CHOWhat is the product (A, B, C, or D) of the reaction shown in Image30? a. C b.D c. B d. A
- Q31. If an excess of HCl (> 2.0 mol equivalents) is added to a mixture of a linear dialkene with 9 carbon atoms, what would be the molecular weight of the resulting product?Answer in g mol-1 to one decimal place please.show how (s)-4-methylpentan-2-ol can be converted into (s)-2-chloro-4-mehtylpentane thank youBy considering the stereochemical requirements for E2-elimination, and using an appropriate illustration need help indicating whether the more stable conformer (conformer B) of trans-1 can undergo E2 elimination. Thank you :)