H₂C isopropoxide a b с + CH3 K d e H3C-I 8+ iodomethane Prelab Question #3 Homework Unanswered Which of the following is true when referring to Figure 3 above. SN2 Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. H3C isopropoxide is the electrophile CH3 transition state Figure 3. A typical SN2 reaction. iodomethane is both the nucleophile and electrophile H 10 there are no electrophiles in Figure 3 the lone pairs of isopropoxide make the molecule nucleophilic iodomethane is the nucleophile because it is accepting electrons CH3 насосно ether product + :1 KⓇ potassium iodide

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The image illustrates a typical SN2 reaction involving isopropoxide and iodomethane.

### Description of Figure 3:

1. **Reactants**:
   - **Isopropoxide ([CH₃₂CHO]⁻)**: Contains a negatively charged oxygen, indicated by the oxygen with a negative charge.
   - **Iodomethane (CH₃I)**: Shows a partial positive charge on iodine (δ⁺).

2. **Mechanism**:
   - The nucleophilic isopropoxide attacks the carbon atom bonded to iodine in iodomethane.
   - The red arrows depict the movement of electrons, where the lone pair of electrons on oxygen forms a bond with the carbon.
   - Simultaneously, the bond between carbon and iodine breaks, releasing iodide (I⁻).

3. **Transition State**:
   - Shows a partial bond formation between oxygen and carbon, and bond breaking between carbon and iodine.

4. **Products**:
   - **Ether Product ([CH₃₂CHOCH₃])**: Formed after the successful nucleophilic attack and release of iodide.
   - **Potassium Iodide (KI)**: Formed by the association of K⁺ with I⁻.

### Prelab Question #3:

#### Which of the following is true when referring to Figure 3 above?

**Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer.**

a. iodomethane is both the nucleophile and electrophile  
b. isopropoxide is the electrophile  
c. the lone pairs of isopropoxide make the molecule nucleophilic  
d. iodomethane is the nucleophile because it is accepting electrons  
e. there are no electrophiles in Figure 3
Transcribed Image Text:The image illustrates a typical SN2 reaction involving isopropoxide and iodomethane. ### Description of Figure 3: 1. **Reactants**: - **Isopropoxide ([CH₃₂CHO]⁻)**: Contains a negatively charged oxygen, indicated by the oxygen with a negative charge. - **Iodomethane (CH₃I)**: Shows a partial positive charge on iodine (δ⁺). 2. **Mechanism**: - The nucleophilic isopropoxide attacks the carbon atom bonded to iodine in iodomethane. - The red arrows depict the movement of electrons, where the lone pair of electrons on oxygen forms a bond with the carbon. - Simultaneously, the bond between carbon and iodine breaks, releasing iodide (I⁻). 3. **Transition State**: - Shows a partial bond formation between oxygen and carbon, and bond breaking between carbon and iodine. 4. **Products**: - **Ether Product ([CH₃₂CHOCH₃])**: Formed after the successful nucleophilic attack and release of iodide. - **Potassium Iodide (KI)**: Formed by the association of K⁺ with I⁻. ### Prelab Question #3: #### Which of the following is true when referring to Figure 3 above? **Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer.** a. iodomethane is both the nucleophile and electrophile b. isopropoxide is the electrophile c. the lone pairs of isopropoxide make the molecule nucleophilic d. iodomethane is the nucleophile because it is accepting electrons e. there are no electrophiles in Figure 3
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