Welcome to all current Chemistry Olympiad competitors and future aspirants! Whether you’re deep in preparation or aiming to join the ranks, challenging yourself with advanced problems is key to success. Below are some carefully selected sample questions with detailed answers to help you on your journey.
Before diving into the answers, we encourage you to try solving these questions on your own. This will help you assess your current knowledge, identify areas for improvement, and ultimately, deepen your understanding of the concepts. Take your time and give it your best shot—only then download the answers to see how you did and where you can improve.
Synthesis of Nylon
Question 1: What are the two main starting materials used in the synthesis of nylon in the experiment? Provide their chemical names and formulas.
Question 2: Describe the type of reaction that occurs when adipoyl chloride and hexamethylenediamine react to form nylon. What is the product of this reaction?
Question 3: Explain the significance of the numbers “6,10” in Nylon-6,10. What do these numbers represent in terms of the structure of the polymer?
Question 4: What properties make nylon a suitable material for applications such as clothing, carpets, and industrial uses?
Question 5: If a student wanted to modify the synthesis of nylon to create Nylon-6,6 instead of Nylon-6,10, what changes would need to be made in the starting materials? Provide a brief explanation.
Synthesis of Aspirin
Question 1: What are the two main reactants used in the synthesis of aspirin? Provide their chemical names and formulas.
Question 2: Why is it important to add a small amount of concentrated sulfuric acid during the synthesis of aspirin?
Question 3: What is the function of acetic anhydride in the aspirin synthesis reaction? Explain in simple terms.
Question 4: Describe one way to purify aspirin once it has been synthesized in the lab.
Question 5: If a student obtained a lower yield of aspirin than expected during the synthesis, what could be a possible reason for this outcome? Provide two possible reasons.
TLC (Thin Layer Chromatography) of Pigments from Spinach
Question 1: What is the purpose of mixing hexane and acetone while grinding the spinach?
Question 2: Why the spotting of samples is done using small capillary?
Question 3: Based on the experiment, how many pigments are present in the spinach sample? Explain your answer.
Question 4: Which spot is the most soluble? Justify your answer.
Question 5: What is the Rf value of the pigment which is the most polar?
Solubility Tests and Recrystallization
Question 1: Based on the experiment, describe the solubility of benzoic acid in cold toluene. Suggest the polarity of benzoic acid.
Question 2: Why is the reaction mixture agitated in a hot water bath?
Question 3: If toluene is changed to ethanol, what would you observe on the solubility of both solvents? Provide justification for your answer.
Question 4: How to recover dissolved benzoic acid from the experiment? Explain and justify the method briefly.
Question 5: Can you suggest the continuity of the experiment in order to collect the purified benzoic acid crystals?
We hope these advanced sample questions and detailed answers help you enhance your preparation for the Chemistry Olympiad. Remember, practice is crucial, so keep challenging yourself and exploring new problems. Good luck, and happy studying!
Feel free to contact us if you need some help and guidance in your academic competitions!
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