Br Br OH NaOH DMF 75 °C H₂S EtOH 0°℃ EtOH A H₂PO4 95 °C KOMO MeOH -10 °C Factor S1 SN2 E1 E2 Subst. of C Strength Nuc/B Solvent Temperature Total Factor S1 S2 E1 E2 Subst. of C Strength Nuc/B Solvent Temperature Total Factor S1 S2 E1 E2 Subst. of C Strength Nuc/B Solvent Temperature Total Factor Sul S2 E1 E2 Subst. of C Strength Nuc/B Solvent Temperature Total Factor S1 Subst. of C Strength Nuc/B Solvent Temperature Total S2 E1 E2

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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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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From the table below, pick 2 reactions and draw the complete, detailed (curved arrow mechanism) for each. Thank you
The image features a worksheet for analyzing chemical reaction mechanisms, specifically focusing on substitution (S\(_\text{N}\)1, S\(_\text{N}\)2) and elimination (E1, E2) reactions. Below is the transcription and description of the components.

**Reactions and Conditions:**

1. **Reaction 1**
   - **Chemical Reaction:** Cyclohexyl chloride with NaOH
   - **Solvent:** DMF
   - **Temperature:** 75°C

2. **Reaction 2**
   - **Chemical Reaction:** Propyl chloride with H\(_2\)S
   - **Solvent:** EtOH
   - **Temperature:** 0°C

3. **Reaction 3**
   - **Chemical Reaction:** Isobutyl bromide with EtOH
   - **Condition:** Heat (Δ)

4. **Reaction 4**
   - **Chemical Reaction:** Benzyl alcohol with H\(_3\)PO\(_4\)
   - **Temperature:** 95°C

5. **Reaction 5**
   - **Chemical Reaction:** Isopropyl bromide with KOMe
   - **Solvent:** MeOH
   - **Temperature:** -10°C

**Analysis Tables:**

Each reaction is followed by a table with columns to evaluate factors affecting the mechanism:

- **Factor**
  - **Substitution of C (carbon)**
  - **Strength of Nucleophile/Base**
  - **Solvent**
  - **Temperature**

- **Outcome**
  - **S\(_\text{N}\)1**
  - **S\(_\text{N}\)2**
  - **E1**
  - **E2**

**Instruction:**
- For question 9, the task is to pick two reactions from problem 8 and draw the complete, detailed (curved arrow mechanism) for each.

This exercise helps students evaluate the conditions and predict the most likely mechanisms to occur in each scenario.
Transcribed Image Text:The image features a worksheet for analyzing chemical reaction mechanisms, specifically focusing on substitution (S\(_\text{N}\)1, S\(_\text{N}\)2) and elimination (E1, E2) reactions. Below is the transcription and description of the components. **Reactions and Conditions:** 1. **Reaction 1** - **Chemical Reaction:** Cyclohexyl chloride with NaOH - **Solvent:** DMF - **Temperature:** 75°C 2. **Reaction 2** - **Chemical Reaction:** Propyl chloride with H\(_2\)S - **Solvent:** EtOH - **Temperature:** 0°C 3. **Reaction 3** - **Chemical Reaction:** Isobutyl bromide with EtOH - **Condition:** Heat (Δ) 4. **Reaction 4** - **Chemical Reaction:** Benzyl alcohol with H\(_3\)PO\(_4\) - **Temperature:** 95°C 5. **Reaction 5** - **Chemical Reaction:** Isopropyl bromide with KOMe - **Solvent:** MeOH - **Temperature:** -10°C **Analysis Tables:** Each reaction is followed by a table with columns to evaluate factors affecting the mechanism: - **Factor** - **Substitution of C (carbon)** - **Strength of Nucleophile/Base** - **Solvent** - **Temperature** - **Outcome** - **S\(_\text{N}\)1** - **S\(_\text{N}\)2** - **E1** - **E2** **Instruction:** - For question 9, the task is to pick two reactions from problem 8 and draw the complete, detailed (curved arrow mechanism) for each. This exercise helps students evaluate the conditions and predict the most likely mechanisms to occur in each scenario.
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