2. Draw products for the following reactions and provide the names for each reaction shown. Include dashes and wedges when needed A. B. C. D. Reaction H₂ Pt H₂O H* HBr Br₂ CC14 Name

Introductory Chemistry: A Foundation
9th Edition
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Donald J. DeCoste
Chapter17: Equilibrium
Section: Chapter Questions
Problem 74AP: . A(n) _______ speeds up a reaction without being consumed.
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**2. Draw products for the following reactions and provide the names for each reaction shown. Include dashes and wedges when needed.**

|       | Reaction                                                                                             | Name |
|-------|-------------------------------------------------------------------------------------------------------|------|
| **A.** | ![Reaction A: Cyclopentene with H₂ over Pt catalyst.](#)                                             |      |
| **B.** | ![Reaction B: 1-Pentene with H₂O in acidic conditions (H⁺).](#)                                       |      |
| **C.** | ![Reaction C: 2-Butyne with HBr.](#)                                                                 |      |
| **D.** | ![Reaction D: Cyclopropylacetylene with Br₂ in CCl₄.](#)                                             |      |
| **E.** | ![Reaction E: 3-Methyl-1-cyclopentene with Br₂ and H₂O.](#)                                          |      |

**Reaction Details:**
- **A:** Hydrogenation of cyclopentene using a platinum catalyst results in cyclopentane.
- **B:** Hydration of 1-pentene under acidic conditions leads to the formation of pentanol.
- **C:** Addition of hydrogen bromide to 2-butyne yields 2-bromo-2-butene.
- **D:** Addition of bromine to cyclopropylacetylene in carbon tetrachloride results in a dibrominated product.
- **E:** Halohydrin formation of 3-methyl-1-cyclopentene using bromine and water gives a bromohydrin compound.
Transcribed Image Text:**2. Draw products for the following reactions and provide the names for each reaction shown. Include dashes and wedges when needed.** | | Reaction | Name | |-------|-------------------------------------------------------------------------------------------------------|------| | **A.** | ![Reaction A: Cyclopentene with H₂ over Pt catalyst.](#) | | | **B.** | ![Reaction B: 1-Pentene with H₂O in acidic conditions (H⁺).](#) | | | **C.** | ![Reaction C: 2-Butyne with HBr.](#) | | | **D.** | ![Reaction D: Cyclopropylacetylene with Br₂ in CCl₄.](#) | | | **E.** | ![Reaction E: 3-Methyl-1-cyclopentene with Br₂ and H₂O.](#) | | **Reaction Details:** - **A:** Hydrogenation of cyclopentene using a platinum catalyst results in cyclopentane. - **B:** Hydration of 1-pentene under acidic conditions leads to the formation of pentanol. - **C:** Addition of hydrogen bromide to 2-butyne yields 2-bromo-2-butene. - **D:** Addition of bromine to cyclopropylacetylene in carbon tetrachloride results in a dibrominated product. - **E:** Halohydrin formation of 3-methyl-1-cyclopentene using bromine and water gives a bromohydrin compound.
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