Carbonyl Compounds III Carbonyl Compounds III – ch. 19 Carbonyl Compounds III – ch. 19 Carbonyl Compounds III – ch. 19 Carbonyl Compounds III – ch. 19

Carbonyl Compounds III Carbonyl Compounds III – ch. 19 Carbonyl Compounds III – ch. 19 Carbonyl Compounds III – ch. 19 Carbonyl Compounds III – ch. 19 www.phwiki.com

Carbonyl Compounds III Carbonyl Compounds III – ch. 19 Carbonyl Compounds III – ch. 19 Carbonyl Compounds III – ch. 19 Carbonyl Compounds III – ch. 19

Paramore, Phil, Host has reference to this Academic Journal, PHwiki organized this Journal Carbonyl Compounds III Chapter 19 Carbonyl Compounds III – ch. 19 1. Rank the following compounds in order of increasing pKa in addition to draw the most likely enol tautomer. Carbonyl Compounds III – ch. 19 2. NMR tests as long as the different types of hydrogen in a compound. Explain how the NMR of cyclohexanone changes after cyclohexanone is allowed to sit in a solution of basic D2O

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Carbonyl Compounds III – ch. 19 3. Predict the product as long as the following reactions. Carbonyl Compounds III – ch. 19 4. Predict the product as long as the following reactions: Carbonyl Compounds III – ch. 19 5. Predict the products as long as the following reactions:

Carbonyl Compounds III – ch. 19 6. Predict the products as long as the following reactions: Carbonyl Compounds III – ch. 19 7. How would you prepare the following compounds from the given starting materials Carbonyl Compounds III – ch. 19 8. Predict the products as long as the following reactions:

Carbonyl Compounds III – ch. 19 9. Predict the products as long as the following reactions: Carbonyl Compounds III – ch. 19 10. Predict the products as long as the following reactions: Carbonyl Compounds III – ch. 19 11. Predict the product as long as the following reactions:

Carbonyl Compounds III – ch. 19 12. Predict the products as long as the following reactions: Carbonyl Compounds III – ch. 19 13. Predict the products as long as the following reactions: Carbonyl Compounds III – ch. 19 14. Predict the product as long as the following reactions:

Carbonyl Compounds III – ch. 19 15. Predict the product as long as the following reactions: Carbonyl Compounds III – ch. 19 16. Predict the product as long as the following reaction: Carbonyl Compounds III – ch. 19 17. Predict the product as long as the following reactions:

Carbonyl Compounds III – ch. 19 18. Which of the following compounds would be expected to decarboxylate when heated. Draw the decarboxylated products if applicable. Carbonyl Compounds III – ch. 19 19. Predict the products as long as the following reactions: Carbonyl Compounds III – ch. 19 20. How would you prepare the following via malonic ester synthesis a. 4-methylpentanoic acid b. 3-phenylpropanoic acid

Carbonyl Compounds III – ch. 19 21. Predict the products as long as the following reactions:

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