Br Br Br Br ОН LOH H2O, H¿SO4 H2 Pd/C 1. ВН+/THF 2. HO¯, H2O2, LOH RÖOOH H2O LOR H. H Name the following compound. CO Br2 H2O Br2 HBr 1. Оз, -78°C 2. (CH3)2S ROH, H,SO4
Br Br Br Br ОН LOH H2O, H¿SO4 H2 Pd/C 1. ВН+/THF 2. HO¯, H2O2, LOH RÖOOH H2O LOR H. H Name the following compound. CO Br2 H2O Br2 HBr 1. Оз, -78°C 2. (CH3)2S ROH, H,SO4
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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Transcribed Image Text:Title: Name the Following Compound
Description: The image presented is a chemical reaction schema revolving around cyclohexene. It includes multiple transformation pathways of cyclohexene, which lead to various organic compounds. Below the schema is the query, "Name the following compound."
Reactions:
1. **Cyclohexene (Starting compound in the center)**:
- Its transformations lead to multiple different products, indicated by arrows.
2. **Pathway 1**:
- Reagent: Br₂, H₂O
- Product: Compound with a bromine atom (Br) attached to one carbon.
3. **Pathway 2**:
- Reagent: H₂, Pd/C
- Product: Cyclohexane.
4. **Pathway 3**:
- Reagent: Br₂ (Bromine)
- Product: Dibromocyclohexane (compound with two bromine atoms attached to two different carbons).
5. **Pathway 4**:
- Reagent: H₂SO₄, H₂O
- Product: Cyclohexanol (compound with hydroxyl group (OH) attached).
6. **Pathway 5**:
- Reagent: 1. BH₃/THF, 2. H₂O₂, OH⁻
- Product: Cyclohexanol with the hydroxyl group (OH) potentially attached to a different carbon compared to Pathway 4.
7. **Pathway 6**:
- Reagent: ROH, H₂SO₄
- Product: Ether derivative with R attached via oxygen.
8. **Pathway 7**:
- Reagent: HBr
- Product: Bromocyclohexane.
9. **Pathway 8**:
- Reagent: (CH₃)₂S
- Product: Epoxide.
10. **Pathway 9**:
- Reagent: RCOOH
- Product: Hydroxy ester.
11. **Pathway 10**:
- Reagent: 1. O₃ (-78 °C), 2. (CH₃)₂S
- Product: Dialdehyde compound.
Explanation:
Each of these pathways represents common organic chemistry transformations involving cyclohexene as the starting material. The image shows the versatility of cycl
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