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Test your understanding with targeted questions related to the topic.
Question 1
Easy
What makes α-hydrogens in aldehydes and ketones acidic?
💡 Hint: Think about what happens to the electron cloud around the carbonyl group.
Question 2
Easy
Name the product of an aldol reaction between two ethanal molecules.
💡 Hint: Combine two ethanal molecules and add a hydroxyl group at the β-position.
Practice 4 more questions and get performance evaluation
Engage in quick quizzes to reinforce what you've learned and check your comprehension.
Question 1
Which condition is necessary for aldol condensation to occur?
💡 Hint: What medium helps form an enolate ion?
Question 2
Cross aldol condensation always results in a single product.
💡 Hint: Think about the number of possible combinations of reactants.
Solve and get performance evaluation
Push your limits with challenges.
Question 1
Predict the products of a cross aldol reaction between cyclopentanone and benzaldehyde.
💡 Hint: Determine which compound forms the enolate and which acts as electrophile.
Question 2
Design a reaction sequence starting from propanal to synthesize an α,β-unsaturated aldehyde via aldol condensation.
💡 Hint: Use the same molecule as both enolate and electrophile.
Challenge and get performance evaluation