:C: H :CI: :CI: H. CH3 C=C H -CI: H3C-C-C-CH H3C CH3 CH3 Add curved arrows for the first step. Draw both the organic ar species. Include nonbonc where applicable. Includ Select Draw Rings More Erase C Cl Select Draw Rings CH, C. H,C CH,

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Chapter1: Chemical Foundations
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**Chemical Reaction Mechanism - Stepwise Illustration**

**Step 1: Curved Arrows Addition**
- **Reactants:**
  - An alkyne molecule with the formula: \(\text{CH}_3-\text{C} \equiv \text{C}-\text{CH}_3\)
  - Hydrochloric acid (\(\text{H-Cl}\))

- **Diagram Description:**
  - The alkyne group is depicted on the left side with the structure \(\text{CH}_3-\text{C} \equiv \text{C}-\text{CH}_3\).
  - The hydrochloric acid molecule (\(\text{H-Cl}\)) is shown with a single bond between Hydrogen and Chlorine, and two lone pairs on Chlorine.
  - There are tools displayed for manipulation, including options to draw bonds, add rings, and select elements like Carbon and Chlorine.

- **Instruction:**
  - "Add curved arrows for the first step."
  - Curved arrows indicate the movement of electron pairs during the reaction.

**Step 2: Intermediate Species Formation**
- **Diagrams:**
  - On the right, the product of the first reaction step shows an addition to the alkyne molecule resulting in a vinyl chloride structure: \(\text{H}_3\text{C}-\overset{\text{H}}{\overset{|}{\text{C}=\text{C}}}-\text{CH}_3\). A chloride ion (\(^-:\text{Cl}\)) with three lone pairs is also depicted.

- **Instruction:**
  - "Draw both the organic and inorganic intermediate species. Include nonbonding electrons and charges where applicable. Include hydrogen atoms."

- **Tools Available:**
  - Options similar to the previous step for drawing, selecting rings, and choosing elements.

**Summary:**
This illustration guides the addition of \(\text{H-Cl}\) to an alkyne, focusing on electron pair movement with curved arrows, and presenting a detailed view of intermediates, including all atoms, nonbonding electrons, and any charges involved in the process.
Transcribed Image Text:**Chemical Reaction Mechanism - Stepwise Illustration** **Step 1: Curved Arrows Addition** - **Reactants:** - An alkyne molecule with the formula: \(\text{CH}_3-\text{C} \equiv \text{C}-\text{CH}_3\) - Hydrochloric acid (\(\text{H-Cl}\)) - **Diagram Description:** - The alkyne group is depicted on the left side with the structure \(\text{CH}_3-\text{C} \equiv \text{C}-\text{CH}_3\). - The hydrochloric acid molecule (\(\text{H-Cl}\)) is shown with a single bond between Hydrogen and Chlorine, and two lone pairs on Chlorine. - There are tools displayed for manipulation, including options to draw bonds, add rings, and select elements like Carbon and Chlorine. - **Instruction:** - "Add curved arrows for the first step." - Curved arrows indicate the movement of electron pairs during the reaction. **Step 2: Intermediate Species Formation** - **Diagrams:** - On the right, the product of the first reaction step shows an addition to the alkyne molecule resulting in a vinyl chloride structure: \(\text{H}_3\text{C}-\overset{\text{H}}{\overset{|}{\text{C}=\text{C}}}-\text{CH}_3\). A chloride ion (\(^-:\text{Cl}\)) with three lone pairs is also depicted. - **Instruction:** - "Draw both the organic and inorganic intermediate species. Include nonbonding electrons and charges where applicable. Include hydrogen atoms." - **Tools Available:** - Options similar to the previous step for drawing, selecting rings, and choosing elements. **Summary:** This illustration guides the addition of \(\text{H-Cl}\) to an alkyne, focusing on electron pair movement with curved arrows, and presenting a detailed view of intermediates, including all atoms, nonbonding electrons, and any charges involved in the process.
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