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What are the products from the following reactions? Please help with d-h

What are the products from the following reactions? Please help with d-h

Chemistry
Chemistry
10th Edition
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
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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What are the products from the following reactions? Please help with d-h
### Transcription of Reactions #### Reaction a) **Reactant:** - Structure: Ethyl group (CH₃CH₂), adjacent to a carbonyl group (C=O), bound to a nitrogen (N) with a methyl group (CH₃) attached. **Conditions:** - Heating with ethyl alcohol (EtOH) and catalytic H⁺. **Product:** - Not specified. #### Reaction b) **Reactant:** - Structure: Aromatic ring with a hydroxyl group (OH) and a carbonyl group (C=O). **Conditions:** - Heated with ethyl alcohol (EtOH) and catalytic HCl. **Product:** - Aromatic ring with an ester group formed (integration of EtO indicates ester). #### Reaction c) **Reactant:** - Structure: Hydroxyethanoic acid with a hydroxyl group (OH) attached. **Conditions:** - Heated with methanol (CH₃OH) and an acid catalyst. **Product:** - Ester formation with a methoxy group replacing the hydroxyl group. #### Reaction d) **Reactant:** - Ethyl benzoate and excess isopropanol. **Conditions:** - In the presence of HCl. **Product:** - Not specified. #### Reaction e) **Reactant:** - Structure: Two aromatic rings bridged by an ethylene group (OH). **Conditions:** - H₂SO₄, methanol, heat. **Product:** - Not specified. #### Reaction f) **Reactant:** - Cyclopentanone structure with a carbonyl group (C=O). **Conditions:** - Undergoes reaction with HCl in H₂O. **Product:** - Not specified. #### Reaction g) **Reactant:** - Aromatic ring with methoxycarbonyl group (CO₂CH₃). **Conditions:** - Reaction with excess C₁₃H₂₆NH₂ (amine). **Product:** - Not specified. #### Reaction h) **Reactants:** - Aromatic ring with hydroxyl group (OH). - Aromatic ring with acyl chloride group (COCl). **Product:** - Not specified. ### Note The products for reactions d), e), f), g), and specific product for h) are not drawn in the provided notes. The reactions seem to involve typical organic transformations
Transcribed Image Text:### Transcription of Reactions #### Reaction a) **Reactant:** - Structure: Ethyl group (CH₃CH₂), adjacent to a carbonyl group (C=O), bound to a nitrogen (N) with a methyl group (CH₃) attached. **Conditions:** - Heating with ethyl alcohol (EtOH) and catalytic H⁺. **Product:** - Not specified. #### Reaction b) **Reactant:** - Structure: Aromatic ring with a hydroxyl group (OH) and a carbonyl group (C=O). **Conditions:** - Heated with ethyl alcohol (EtOH) and catalytic HCl. **Product:** - Aromatic ring with an ester group formed (integration of EtO indicates ester). #### Reaction c) **Reactant:** - Structure: Hydroxyethanoic acid with a hydroxyl group (OH) attached. **Conditions:** - Heated with methanol (CH₃OH) and an acid catalyst. **Product:** - Ester formation with a methoxy group replacing the hydroxyl group. #### Reaction d) **Reactant:** - Ethyl benzoate and excess isopropanol. **Conditions:** - In the presence of HCl. **Product:** - Not specified. #### Reaction e) **Reactant:** - Structure: Two aromatic rings bridged by an ethylene group (OH). **Conditions:** - H₂SO₄, methanol, heat. **Product:** - Not specified. #### Reaction f) **Reactant:** - Cyclopentanone structure with a carbonyl group (C=O). **Conditions:** - Undergoes reaction with HCl in H₂O. **Product:** - Not specified. #### Reaction g) **Reactant:** - Aromatic ring with methoxycarbonyl group (CO₂CH₃). **Conditions:** - Reaction with excess C₁₃H₂₆NH₂ (amine). **Product:** - Not specified. #### Reaction h) **Reactants:** - Aromatic ring with hydroxyl group (OH). - Aromatic ring with acyl chloride group (COCl). **Product:** - Not specified. ### Note The products for reactions d), e), f), g), and specific product for h) are not drawn in the provided notes. The reactions seem to involve typical organic transformations
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