11. (Chapter 13) Under what conditions would the reaction of a carbonyl group continue after resolving the negative formal charge of a tetrahedral intermediate by adding a hydrogen ion? 12. (Chapter 8) Draw the individual resonance contributors for the following intermediate. Label the individual contributors as major or minor, and then draw a representation of the actual structure. CH2 Additional Contributors: Actual Molecule: 13. (Chapter 13) What is the stereochemistry of the product when 1 chirality center is created by reacting (R)-3-bromo-3-methylhexane with a protic polar solvent?

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11. (Chapter 13) Under what conditions would the reaction of a carbonyl group continue after
resolving the negative formal charge of a tetrahedral intermediate by adding a hydrogen ion?
12. (Chapter 8) Draw the individual resonance contributors for the following intermediate. Label
the individual contributors as major or minor, and then draw a representation of the actual
structure.
CH2
Additional Contributors:
Actual Molecule:
13. (Chapter 13) What is the stereochemistry of the product when 1 chirality center is created by
reacting (R)-3-bromo-3-methylhexane with a protic polar solvent?
Transcribed Image Text:11. (Chapter 13) Under what conditions would the reaction of a carbonyl group continue after resolving the negative formal charge of a tetrahedral intermediate by adding a hydrogen ion? 12. (Chapter 8) Draw the individual resonance contributors for the following intermediate. Label the individual contributors as major or minor, and then draw a representation of the actual structure. CH2 Additional Contributors: Actual Molecule: 13. (Chapter 13) What is the stereochemistry of the product when 1 chirality center is created by reacting (R)-3-bromo-3-methylhexane with a protic polar solvent?
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