Draw the structures of the missing reactants, intermediates, or products in the following mechanism. Include all lone pairs. Ignore stereochemistry. Ignore inorganic byproducts. Н. BH2 H. BH2 THE

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Draw the strcutres of the missing reactants, intermediates, or products in the following mechanisms. Include all lone pairs. 

### Transcription for Educational Context

**Instructions:**

Draw the structures of the missing reactants, intermediates, or products in the following mechanism. Include all lone pairs. Ignore stereochemistry. Ignore inorganic byproducts.

**Description of Diagram:**

The diagram illustrates a chemical reaction mechanism involving an alkene and borane (BH₂). 

1. **Initial Structure:**
   - Starts with an alkene containing a carbon-carbon double bond.

2. **Reaction with Borane:**
   - The first step involves the addition of borane (BH₂) across the double bond of the alkene. An arrow indicates the movement of a hydrogen (H) from the BH₂ to the adjacent carbon, forming a new bond.

3. **Intermediate Structure:**
   - Formation of a cyclic structure where BH₂ is now bonded to one of the carbons previously involved in the double bond, and hydrogen is bonded to the other carbon.

4. **Arrow Indicating Progression:**
   - A vertical arrow signifies the progression to the next step or reaction.

5. **Additional Reagent:**
   - Tetrahydrofuran (THF) is indicated as a solvent or possible reagent involved in the process.

This mechanism is a typical illustration of a hydroboration reaction where the addition of borane to an alkene is followed by further reactions that are not depicted but could proceed to other products.
Transcribed Image Text:### Transcription for Educational Context **Instructions:** Draw the structures of the missing reactants, intermediates, or products in the following mechanism. Include all lone pairs. Ignore stereochemistry. Ignore inorganic byproducts. **Description of Diagram:** The diagram illustrates a chemical reaction mechanism involving an alkene and borane (BH₂). 1. **Initial Structure:** - Starts with an alkene containing a carbon-carbon double bond. 2. **Reaction with Borane:** - The first step involves the addition of borane (BH₂) across the double bond of the alkene. An arrow indicates the movement of a hydrogen (H) from the BH₂ to the adjacent carbon, forming a new bond. 3. **Intermediate Structure:** - Formation of a cyclic structure where BH₂ is now bonded to one of the carbons previously involved in the double bond, and hydrogen is bonded to the other carbon. 4. **Arrow Indicating Progression:** - A vertical arrow signifies the progression to the next step or reaction. 5. **Additional Reagent:** - Tetrahydrofuran (THF) is indicated as a solvent or possible reagent involved in the process. This mechanism is a typical illustration of a hydroboration reaction where the addition of borane to an alkene is followed by further reactions that are not depicted but could proceed to other products.
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