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2. Fill in each box with the expected organic product of the indicated multistep transformation. Be sure that each product you draw takes into account all steps of the transformation, including workup steps! Remember to account for stereochemistry where appropriate. a. Но. 1. LIAIH4 (excess), Et20 2. H* workup b. 1. MeLi (excess), Et20 2. H* workup EtO 3. CrO3, pyridine С. 1. H3O* CN 2. SOC2

2. Fill in each box with the expected organic product of the indicated multistep transformation. Be sure that each product you draw takes into account all steps of the transformation, including workup steps! Remember to account for stereochemistry where appropriate. a. Но. 1. LIAIH4 (excess), Et20 2. H* workup b. 1. MeLi (excess), Et20 2. H* workup EtO 3. CrO3, pyridine С. 1. H3O* CN 2. SOC2

Chemistry
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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Can you please show me the organic products for these reactants and reagents?

**Educational Website Transcription: Organic Chemistry Reactions and Mechanisms** **2. Reaction Scheme: Determine the Organic Product** Carefully analyze each reaction sequence below. Your task is to identify the major organic product formed after each multistep transformation, considering each step and any stereochemical implications. a. **Starting Material:** - Structure: A hydroxy acid with a piperidinone ring, possessing a hydroxyl group on the ring. - Reagents: 1. Excess LiAlH₄ (in ether, Et₂O) 2. H₃O⁺ workup b. **Starting Material:** - Structure: An ester group connected to a dicarboxylic acid. - Reagents: 1. Excess MeLi (in ether, Et₂O) 2. H⁺ workup 3. CrO₃, pyridine c. **Starting Material:** - Structure: A nitrile group attached to a butane backbone. - Reagents: 1. H₃O⁺ 2. SOCl₂ d. **Starting Material:** - Structure: A phthalimide derivative. - Reagents: 1. NaOH, H₂O 2. H⁺ workup 3. LiAlH₄ (in ether, Et₂O) 4. H⁺ workup e. **Starting Material:** - Structure: A ketone with an acyl group. - Reagents: 1. NaCN, EtOH, heated to 80 °C 2. LiAlH₄ (in ether, Et₂O) 3. H⁺ workup **Instructions:** In each scenario, draw the expected organic product at the end of the arrow. Consider all transformative steps and workups to identify the final structure. Note how the stereochemistry, if pertinent, is affected or retained throughout the reactions.
Transcribed Image Text:**Educational Website Transcription: Organic Chemistry Reactions and Mechanisms** **2. Reaction Scheme: Determine the Organic Product** Carefully analyze each reaction sequence below. Your task is to identify the major organic product formed after each multistep transformation, considering each step and any stereochemical implications. a. **Starting Material:** - Structure: A hydroxy acid with a piperidinone ring, possessing a hydroxyl group on the ring. - Reagents: 1. Excess LiAlH₄ (in ether, Et₂O) 2. H₃O⁺ workup b. **Starting Material:** - Structure: An ester group connected to a dicarboxylic acid. - Reagents: 1. Excess MeLi (in ether, Et₂O) 2. H⁺ workup 3. CrO₃, pyridine c. **Starting Material:** - Structure: A nitrile group attached to a butane backbone. - Reagents: 1. H₃O⁺ 2. SOCl₂ d. **Starting Material:** - Structure: A phthalimide derivative. - Reagents: 1. NaOH, H₂O 2. H⁺ workup 3. LiAlH₄ (in ether, Et₂O) 4. H⁺ workup e. **Starting Material:** - Structure: A ketone with an acyl group. - Reagents: 1. NaCN, EtOH, heated to 80 °C 2. LiAlH₄ (in ether, Et₂O) 3. H⁺ workup **Instructions:** In each scenario, draw the expected organic product at the end of the arrow. Consider all transformative steps and workups to identify the final structure. Note how the stereochemistry, if pertinent, is affected or retained throughout the reactions.
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