Exam 22: The Chemistry of Enolate Ions, Enols, and Α,β-Unsaturated Carbonyl Compounds
Exam 1: Chemical Bonding and Chemical Structure26 Questions
Exam 2: Alkanes and Organic Nomenclature25 Questions
Exam 3: The Curved-Arrow Notation, Resonance, Acids and Bases, and Chemical Equilibrium25 Questions
Exam 4: Introduction to Alkenes and Alkynes26 Questions
Exam 5: Addition Reactions of Alkenes and Alkynes25 Questions
Exam 6: Principles of Stereochemistry25 Questions
Exam 7: Cyclic Compounds and Reaction Stereochemistry25 Questions
Exam 8: Nomenclature and Noncovalent Intermolecular Interactions25 Questions
Exam 9: The Chemistry of Alkyl Halides25 Questions
Exam 10: Free-Radical Reactions, Main-Group Organometallic Compounds, and Carbenes25 Questions
Exam 11: The Chemistry of Alcohols and Thiols25 Questions
Exam 12: The Chemistry of Ethers, Epoxides, Glycols, and Sulfides25 Questions
Exam 13: Introduction to Spectroscopy25 Questions
Exam 14: Nuclear Magnetic Resonance Spectroscopy27 Questions
Exam 15: Dienes and Aromaticity25 Questions
Exam 16: The Chemistry of Benzene and Its Derivatives24 Questions
Exam 17: Allylic and Benzylic Reactivity25 Questions
Exam 18: The Chemistry of Aryl Halides, Vinylic Halides, and Phenols25 Questions
Exam 19: The Chemistry of Aldehydes and Ketones25 Questions
Exam 20: The Chemistry of Carboxylic Acids25 Questions
Exam 21: The Chemistry of Carboxylic Acid Derivatives25 Questions
Exam 22: The Chemistry of Enolate Ions, Enols, and Α,β-Unsaturated Carbonyl Compounds25 Questions
Exam 23: The Chemistry of Amines25 Questions
Exam 24: Carbohydrates25 Questions
Exam 25: The Chemistry of Thioesters, Phosphate Esters, and Phosphate Anhydrides25 Questions
Exam 26: The Chemistry of the Aromatic Heterocycles and Nucleic Acids25 Questions
Exam 27: Amino Acids, Peptides, and Proteins25 Questions
Exam 28: Pericyclic Reactions25 Questions
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This compound can be formed from a condensation reaction. Name the reaction and draw the precursor to the condensation reaction.


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Outline a synthesis for the transformation of acetone to a tertiary alcohol. The phenyl group should come from PhLi.


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Can this compound be prepared in good yield by an aldol reaction? If so, give the starting materials. If not, explain why.


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Predict the major organic product for the reaction. If you believe no reaction would occur, write NR.


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