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The compound being analyzed is HC H CH || HC C' H H H₁₂ 1. Provide a correct name for the structure. 2. Write its molecular formula. 3. Calculate its whole number molecular weight. Use C=12, H=1, O=16. 4. Write a complete equation for its hydration in acidic solution. 5. Write a complete equation for its hydration in basic solution. 6. Write a complete equation for its cyanohydrin formation. 7. Write a complete equation for its PTSA-catalyzed reaction with 1-butanol to form the hemiacetal. 8. Write a complete equation for its PTSA-catalyzed reaction with two equivalents of methanol to form the acetal. 9. Draw all the enols that the compound forms. 10. Write a complete equation for the enolate that forms when the compound is reacted with hydroxide. 11. Write a complete equation for the reaction of the enolate in '10' with Cl₂. 12. Write a complete equation for the reaction of the enolate in '10' with 1- bromo-cyclopentane. 13. Write a complete equation for the aldol condensation reaction that occurs when two equivalents of the compound react with each other in 50% NaOH followed by heating.

The compound being analyzed is HC H CH || HC C' H H H₁₂ 1. Provide a correct name for the structure. 2. Write its molecular formula. 3. Calculate its whole number molecular weight. Use C=12, H=1, O=16. 4. Write a complete equation for its hydration in acidic solution. 5. Write a complete equation for its hydration in basic solution. 6. Write a complete equation for its cyanohydrin formation. 7. Write a complete equation for its PTSA-catalyzed reaction with 1-butanol to form the hemiacetal. 8. Write a complete equation for its PTSA-catalyzed reaction with two equivalents of methanol to form the acetal. 9. Draw all the enols that the compound forms. 10. Write a complete equation for the enolate that forms when the compound is reacted with hydroxide. 11. Write a complete equation for the reaction of the enolate in '10' with Cl₂. 12. Write a complete equation for the reaction of the enolate in '10' with 1- bromo-cyclopentane. 13. Write a complete equation for the aldol condensation reaction that occurs when two equivalents of the compound react with each other in 50% NaOH followed by heating.

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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The compound being analyzed is HC H CH || HC C' H H H₁₂ 1. Provide a correct name for the structure. 2. Write its molecular formula. 3. Calculate its whole number molecular weight. Use C=12, H=1, O=16. 4. Write a complete equation for its hydration in acidic solution. 5. Write a complete equation for its hydration in basic solution. 6. Write a complete equation for its cyanohydrin formation. 7. Write a complete equation for its PTSA-catalyzed reaction with 1-butanol to form the hemiacetal. 8. Write a complete equation for its PTSA-catalyzed reaction with two equivalents of methanol to form the acetal. 9. Draw all the enols that the compound forms. 10. Write a complete equation for the enolate that forms when the compound is reacted with hydroxide. 11. Write a complete equation for the reaction of the enolate in '10' with Cl₂. 12. Write a complete equation for the reaction of the enolate in '10' with 1- bromo-cyclopentane. 13. Write a complete equation for the aldol condensation reaction that occurs when two equivalents of the compound react with each other in 50% NaOH followed by heating.
Transcribed Image Text:The compound being analyzed is HC H CH || HC C' H H H₁₂ 1. Provide a correct name for the structure. 2. Write its molecular formula. 3. Calculate its whole number molecular weight. Use C=12, H=1, O=16. 4. Write a complete equation for its hydration in acidic solution. 5. Write a complete equation for its hydration in basic solution. 6. Write a complete equation for its cyanohydrin formation. 7. Write a complete equation for its PTSA-catalyzed reaction with 1-butanol to form the hemiacetal. 8. Write a complete equation for its PTSA-catalyzed reaction with two equivalents of methanol to form the acetal. 9. Draw all the enols that the compound forms. 10. Write a complete equation for the enolate that forms when the compound is reacted with hydroxide. 11. Write a complete equation for the reaction of the enolate in '10' with Cl₂. 12. Write a complete equation for the reaction of the enolate in '10' with 1- bromo-cyclopentane. 13. Write a complete equation for the aldol condensation reaction that occurs when two equivalents of the compound react with each other in 50% NaOH followed by heating.
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