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### Tetrahydropyran Reaction with Chlorine and Water

#### Reaction Overview:
The diagram illustrates the reaction of 4-methylcyclopentene with chlorine (Cl₂) in the presence of water (H₂O), resulting in the formation of various products.

#### Molecule Structures:
The reactant and resulting products are depicted as follows:

1. **Reactant:**
   - 4-methylcyclopentene, which is a five-membered cyclopentane ring featuring a double bond and a methyl group attached to one of the carbon atoms in the ring.

2. **Products:**
   - **(a)** Cl on wedge at carbon 1, Cl on dash at carbon 2.
   - **(b)** Cl on wedge at carbon 1, Cl on wedge at carbon 2.
   - **(c)** Cl on wedge at carbon 1, OH on dash at carbon 2.
   - **(d)** Cl on dash at carbon 1, OH on wedge at carbon 2.
   - **(e)** OH on wedge at carbon 1, Cl on wedge at carbon 2.
   - **(f)** OH on wedge at carbon 1, Cl on dash at carbon 2.

#### Stereochemistry:
The diagrams represent different stereoisomers of the resultant products, indicating the configuration of chlorine and hydroxyl (OH) groups attached to the cyclopentane ring. The wedges and dashes represent groups oriented above and below the plane of the ring respectively, demonstrating the stereochemistry involved in the reaction.

In this educational content, students can observe the possible outcomes of the chlorohydroxylation reaction and understand the importance of stereochemistry in chemical reactions. Exploring the specific arrangement and orientation of atoms helps in understanding how different reaction conditions can lead to various stereoisomers.
Transcribed Image Text:### Tetrahydropyran Reaction with Chlorine and Water #### Reaction Overview: The diagram illustrates the reaction of 4-methylcyclopentene with chlorine (Cl₂) in the presence of water (H₂O), resulting in the formation of various products. #### Molecule Structures: The reactant and resulting products are depicted as follows: 1. **Reactant:** - 4-methylcyclopentene, which is a five-membered cyclopentane ring featuring a double bond and a methyl group attached to one of the carbon atoms in the ring. 2. **Products:** - **(a)** Cl on wedge at carbon 1, Cl on dash at carbon 2. - **(b)** Cl on wedge at carbon 1, Cl on wedge at carbon 2. - **(c)** Cl on wedge at carbon 1, OH on dash at carbon 2. - **(d)** Cl on dash at carbon 1, OH on wedge at carbon 2. - **(e)** OH on wedge at carbon 1, Cl on wedge at carbon 2. - **(f)** OH on wedge at carbon 1, Cl on dash at carbon 2. #### Stereochemistry: The diagrams represent different stereoisomers of the resultant products, indicating the configuration of chlorine and hydroxyl (OH) groups attached to the cyclopentane ring. The wedges and dashes represent groups oriented above and below the plane of the ring respectively, demonstrating the stereochemistry involved in the reaction. In this educational content, students can observe the possible outcomes of the chlorohydroxylation reaction and understand the importance of stereochemistry in chemical reactions. Exploring the specific arrangement and orientation of atoms helps in understanding how different reaction conditions can lead to various stereoisomers.
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