Alkenes can be converted into alcohols by acid-catalyzed addition

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Assuming that Markovnikov’s rule is valid, predict the major alcohol product from the following alkene.

### Acid-Catalyzed Hydration of Alkenes

**Concept:** Alkenes can be converted into alcohols by acid-catalyzed addition of water.

#### Problem Statement:
Assuming that Markovnikov’s rule is valid, predict the major alcohol product for the given alkene.

#### Diagram:
The image provides a structural diagram of an alkene with the following geometry:

```
    /\
   /  \
  /    \ - - - -
 |       
```

This structural diagram represents a typical linear alkene structure.

#### Considerations:
- **You do not have to consider stereochemistry.**
- **In cases where there is more than one answer, just draw one.**
- **Remember to consider hydride and alkyl shifts.**

#### Markovnikov’s Rule:
When an unsymmetrical alkene undergoes hydrohalogenation or hydration, the hydrogen (H) atom will attach to the less substituted carbon of the double bond, and the hydroxy group (OH) will attach to the more substituted carbon.

#### Steps:
1. **Identify the double bond:** Look at the structure where the double bond is located.
2. **Apply Markovnikov's rule:** Determine the more substituted carbon where the hydroxyl group (OH) will be added.
3. **Predict the major product:** Draw the structure with the hydroxyl group attached to the more substituted carbon atom.

#### Example Structure:
For the provided alkene structure, identify the points of attachment based on the rule, then draw the major alcohol product considering any possible shift (hydride or alkyl) if needed.

**Note:** The image also shows a drawing tool palette at the bottom of the page, which includes various tools for creating chemical structures and notations.

#### Final Note:
Understanding this concept is crucial for predicting the products of alkene reactions and is fundamental in organic chemistry synthesis problems. Remember, practice applying these rules to different structures to reinforce your learning.
Transcribed Image Text:### Acid-Catalyzed Hydration of Alkenes **Concept:** Alkenes can be converted into alcohols by acid-catalyzed addition of water. #### Problem Statement: Assuming that Markovnikov’s rule is valid, predict the major alcohol product for the given alkene. #### Diagram: The image provides a structural diagram of an alkene with the following geometry: ``` /\ / \ / \ - - - - | ``` This structural diagram represents a typical linear alkene structure. #### Considerations: - **You do not have to consider stereochemistry.** - **In cases where there is more than one answer, just draw one.** - **Remember to consider hydride and alkyl shifts.** #### Markovnikov’s Rule: When an unsymmetrical alkene undergoes hydrohalogenation or hydration, the hydrogen (H) atom will attach to the less substituted carbon of the double bond, and the hydroxy group (OH) will attach to the more substituted carbon. #### Steps: 1. **Identify the double bond:** Look at the structure where the double bond is located. 2. **Apply Markovnikov's rule:** Determine the more substituted carbon where the hydroxyl group (OH) will be added. 3. **Predict the major product:** Draw the structure with the hydroxyl group attached to the more substituted carbon atom. #### Example Structure: For the provided alkene structure, identify the points of attachment based on the rule, then draw the major alcohol product considering any possible shift (hydride or alkyl) if needed. **Note:** The image also shows a drawing tool palette at the bottom of the page, which includes various tools for creating chemical structures and notations. #### Final Note: Understanding this concept is crucial for predicting the products of alkene reactions and is fundamental in organic chemistry synthesis problems. Remember, practice applying these rules to different structures to reinforce your learning.
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