Exam 19: Condensation and Conjugate Addition Reactions of Carbonyl Compounds
Exam 1: The Basics158 Questions
Exam 2: Families of Carbon151 Questions
Exam 3: Acids and Bases149 Questions
Exam 4: Nomenclature and Conformations of Alkanes and Cycloalkanes163 Questions
Exam 5: Stereochemistry179 Questions
Exam 6: Nucleophilic Reactions91 Questions
Exam 7: Alkenes and Alkynes I220 Questions
Exam 8: Alkenes and Alkynes II163 Questions
Exam 9: Nuclear Magnetic Resonance and Mass Spectrometry158 Questions
Exam 10: Radical Reactions148 Questions
Exam 11: Alcohols and Ethers256 Questions
Exam 12: Alcohols From Carbonyl Compounds210 Questions
Exam 13: Conjugated Unsaturated Systems201 Questions
Exam 14: Aromatic Compounds186 Questions
Exam 15: Reactions of Aromatic Compounds207 Questions
Exam 16: Aldehydes and Ketones189 Questions
Exam 17: Carboxylic Acids and Their Derivatives213 Questions
Exam 18: Reactions at the Α Carbon of Carbonyl Compounds190 Questions
Exam 19: Condensation and Conjugate Addition Reactions of Carbonyl Compounds182 Questions
Exam 20: Amines207 Questions
Exam 21: Transition Metal Complexes86 Questions
Exam 22: Carbohydrates124 Questions
Exam 23: Lipids127 Questions
Exam 24: Amino Acids and Proteins135 Questions
Exam 25: Nucleic Acids and Protein Synthesis126 Questions
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In the Claisen-Schmidt condensation of 1 mole of acetone with 2 moles of 4-methylbenzaldehyde what is the relationship between the products formed?
(Multiple Choice)
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An aldol reaction that starts with two different carbonyl compounds is called a ___.
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What is the product of the Dieckmann condensation of this diester, 

(Multiple Choice)
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Which of these is a product of the reaction of C6H5MgBr with 

(Multiple Choice)
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The sequence of a Michael addition followed by an intramolecular aldol condensation is known as a ___.
(Short Answer)
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What would be the product,C,of the following reaction sequence? 

(Multiple Choice)
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When acetaldehyde is reacted with 3 equivalents of formaldehyde under alkaline conditions,followed by treatment with sodium borohydride,the product formed shows the following spectra data:
IR: broad peak at 3326 cm−1
1H NMR: singlet at 3.45
singlet at 4.78 (found to be exchangeable)
Predict a reasonable structure for this product.
(Essay)
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What is the product of the following reaction sequence? Give structural details of all significant intermediates. 

(Essay)
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Suggest a reasonable synthetic strategy to carry out the following transformation. 

(Essay)
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Suggest a reasonable synthetic strategy to carry out the following transformation. 

(Essay)
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What would be the product,C,of the following reaction sequence? 

(Multiple Choice)
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Which of these combinations is not one which would result in the formation of essentially one Claisen condensation product when one compound is added slowly to the mixture of the other and the base employed?
(Multiple Choice)
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