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1. For the following reactions, please provide the products by drawing them in the be provided. 2 Na, MeOH NH3 (1) Ome or OH 2 Na, MEOH NH3 (0) OH ov Omé or HO. OMe 2 Na, MeOH NH3 (1) Pera OH

1. For the following reactions, please provide the products by drawing them in the be provided. 2 Na, MeOH NH3 (1) Ome or OH 2 Na, MEOH NH3 (0) OH ov Omé or HO. OMe 2 Na, MeOH NH3 (1) Pera OH

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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Hello,

Can someone please help me, We are learning this new material and for the product I think i am somewhat close but I am not sure. Can someone please explain where I am going wrong or if I am right how to better determine placement, please. 

### Reactions and Products The image presents a series of chemical reactions involving benzene derivatives with sodium (Na), methanol (MeOH), and ammonia (NH₃). #### Reaction 1: - **Reactants:** A benzene ring with a substituent group. - **Reaction Conditions:** 2 equivalents of Na, MeOH, and NH₃ (in liquid form). - **Product Drawing:** The box shows a benzene ring with substituents labeled as "OMe or OH." #### Reaction 2: - **Reactants:** A benzene ring with an ester group (O=C-O) and a ketone group (O=C-CH₃). - **Reaction Conditions:** 2 equivalents of Na, MeOH, and NH₃ (in liquid form). - **Product Drawing:** The box contains a benzene ring with an alcohol group (O-H) and structures labeled "OMe" and "OH" on the transformed ester group. #### Reaction 3: - **Reactants:** A benzene ring with a ketone functional group and an ester group. - **Reaction Conditions:** 2 equivalents of Na, MeOH, and NH₃ (in liquid form). - **Product Drawing:** The product shows a benzene ring with an ester group reduction depicted by a methoxy group (OMe) and hydroxyl group (OH). ### Annotations: - The handwritten notes mention "NaOH" and "NaH", suggesting alternative reagents or by-products. - Red and green arrows are drawn to possibly indicate reaction pathways or atom transfers. - There is a mix of mechanical and handwritten parts showing structures and potential products. These transformations typically involve reductions or nucleophilic substitutions facilitated by the presence of sodium and methoxide ions in an ammonia solvent system. The details of exact structures and annotations indicate the target functional group transformations for these aromatic compounds.
Transcribed Image Text:### Reactions and Products The image presents a series of chemical reactions involving benzene derivatives with sodium (Na), methanol (MeOH), and ammonia (NH₃). #### Reaction 1: - **Reactants:** A benzene ring with a substituent group. - **Reaction Conditions:** 2 equivalents of Na, MeOH, and NH₃ (in liquid form). - **Product Drawing:** The box shows a benzene ring with substituents labeled as "OMe or OH." #### Reaction 2: - **Reactants:** A benzene ring with an ester group (O=C-O) and a ketone group (O=C-CH₃). - **Reaction Conditions:** 2 equivalents of Na, MeOH, and NH₃ (in liquid form). - **Product Drawing:** The box contains a benzene ring with an alcohol group (O-H) and structures labeled "OMe" and "OH" on the transformed ester group. #### Reaction 3: - **Reactants:** A benzene ring with a ketone functional group and an ester group. - **Reaction Conditions:** 2 equivalents of Na, MeOH, and NH₃ (in liquid form). - **Product Drawing:** The product shows a benzene ring with an ester group reduction depicted by a methoxy group (OMe) and hydroxyl group (OH). ### Annotations: - The handwritten notes mention "NaOH" and "NaH", suggesting alternative reagents or by-products. - Red and green arrows are drawn to possibly indicate reaction pathways or atom transfers. - There is a mix of mechanical and handwritten parts showing structures and potential products. These transformations typically involve reductions or nucleophilic substitutions facilitated by the presence of sodium and methoxide ions in an ammonia solvent system. The details of exact structures and annotations indicate the target functional group transformations for these aromatic compounds.
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