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C10H16B12 C C10H160 1. В1з, THF C10H180 F 2. Н2О2, НО E Br2 CH3CO0OH Br2 а-pinene C10H16 1. OsO4 C10H17OB. C10H1802 2. NaHSO3 H20 В A 1) Hg(ОАс)2, Н29 2) NaBH4 1. Оз 2. (CHз)2S C10H180 G C-ト `CH3

C10H16B12 C C10H160 1. В1з, THF C10H180 F 2. Н2О2, НО E Br2 CH3CO0OH Br2 а-pinene C10H16 1. OsO4 C10H17OB. C10H1802 2. NaHSO3 H20 В A 1) Hg(ОАс)2, Н29 2) NaBH4 1. Оз 2. (CHз)2S C10H180 G C-ト `CH3

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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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Give the structures for the compounds A-G in the following reaction scheme. 

The image depicts a reaction scheme involving the compound α-pinene (C₁₀H₁₆), with several possible reaction pathways leading to various products. Below is a detailed transcription of the scheme, including reagents used in each step: 1. **α-Pinene (C₁₀H₁₆) - Starting Material A** - **Reaction with Br₂ and H₂O:** - Product formed: C₁₀H₁₇OBr (Product B) - **Reaction with Br₂:** - Product formed: C₁₀H₁₆Br₂ (Product C) - **Reaction with CH₃COOOH:** - Product formed: C₁₀H₁₆O (Product F) - **Oxidative ozonolysis (1. O₃; 2. (CH₃)₂S):** - A ketone product is formed, as shown by the structure with two carbonyl groups (Product structure shown). 2. **Further Transformations:** - **From C₁₀H₁₇OBr (Product B):** - **Reaction with 1. OsO₄, 2. NaHSO₃:** - Product formed: C₁₀H₁₈O₂ (Product D) - **From C₁₀H₁₇OBr (Product B):** - **Reaction with 1. BH₃, THF; 2. H₂O₂, HO⁻:** - Product formed: C₁₀H₁₈O (Product E) - **From C₁₀H₁₆ (α-Pinene):** - **Reaction with 1. Hg(OAc)₂, H₂O; 2. NaBH₄:** - Product formed: C₁₀H₁₈O (Product G) Each reaction pathway demonstrates different chemical transformations of α-pinene involving halogenation, epoxidation, hydration, and oxidation leading to alcohols, bromohydrins, and other oxygenated products.
Transcribed Image Text:The image depicts a reaction scheme involving the compound α-pinene (C₁₀H₁₆), with several possible reaction pathways leading to various products. Below is a detailed transcription of the scheme, including reagents used in each step: 1. **α-Pinene (C₁₀H₁₆) - Starting Material A** - **Reaction with Br₂ and H₂O:** - Product formed: C₁₀H₁₇OBr (Product B) - **Reaction with Br₂:** - Product formed: C₁₀H₁₆Br₂ (Product C) - **Reaction with CH₃COOOH:** - Product formed: C₁₀H₁₆O (Product F) - **Oxidative ozonolysis (1. O₃; 2. (CH₃)₂S):** - A ketone product is formed, as shown by the structure with two carbonyl groups (Product structure shown). 2. **Further Transformations:** - **From C₁₀H₁₇OBr (Product B):** - **Reaction with 1. OsO₄, 2. NaHSO₃:** - Product formed: C₁₀H₁₈O₂ (Product D) - **From C₁₀H₁₇OBr (Product B):** - **Reaction with 1. BH₃, THF; 2. H₂O₂, HO⁻:** - Product formed: C₁₀H₁₈O (Product E) - **From C₁₀H₁₆ (α-Pinene):** - **Reaction with 1. Hg(OAc)₂, H₂O; 2. NaBH₄:** - Product formed: C₁₀H₁₈O (Product G) Each reaction pathway demonstrates different chemical transformations of α-pinene involving halogenation, epoxidation, hydration, and oxidation leading to alcohols, bromohydrins, and other oxygenated products.
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