(5) 131 1200 C H₂C HO CH. H₂PO heat N₂00(CH) (CH COH Ju CH ESO heat HPO heef

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.  Each of the following alcohols or alkyl halides has been subjected to either acid-catalyzed dehydration or base dehydrohalogenation respectively and yields a mixture of two or more isomeric alkenes.  Identify the  alkenes in each case, and predict which one is the major product on the basis of either Zaitsev rule, stability of the alkene or rearrangement.  Give the IUPAC name, including stereochemistry where necessary, of each organic reactant and product and state whether it is the E1 or E2 product

### Transcription and Explanation for Chemistry Reactions

#### Reaction Schemes

1. **Figure (e):**
   - The structure shown is a cycloalkane with a hydroxyl group (OH) and a methyl group (CH₃) attached to one of its carbon atoms. The reaction involves heating this compound in the presence of phosphoric acid (H₃PO₄).

2. **Figure (f):**
   - This scheme features a cycloalkane with a chlorine (Cl) substituent. The reaction involves sodium methoxide (NaOCH₃) and acetic acid (CH₃COOH) as reactants.

3. **Figure (g):**
   - The compound is a cycloalkane with a chlorine group (Cl) and two methyl groups at the adjacent carbon. The reaction involves heating with sulfuric acid (H₂SO₄).

4. **Figure (h):**
   - The structure here is a linear alkane with a chlorine substituent. The reaction involves heating with phosphoric acid (H₃PO₄).

#### Process Overview

- **Heating and Acid Catalysts:** Each reaction involves heating the compound in the presence of an acid, which is a common method to facilitate elimination reactions leading to dehydration or dehydrohalogenation.
  
- **Common Outcomes:**
  - **Dehydration (e and h):** Likely leads to the loss of a water molecule, resulting in an alkene.
  - **Dehydrohalogenation (f and g):** Likely results in the removal of a hydrogen and a halogen, forming an alkene.

These reactions are typical examples of organic transformation processes used in synthesis and provide insight into mechanisms like elimination and substitution.
Transcribed Image Text:### Transcription and Explanation for Chemistry Reactions #### Reaction Schemes 1. **Figure (e):** - The structure shown is a cycloalkane with a hydroxyl group (OH) and a methyl group (CH₃) attached to one of its carbon atoms. The reaction involves heating this compound in the presence of phosphoric acid (H₃PO₄). 2. **Figure (f):** - This scheme features a cycloalkane with a chlorine (Cl) substituent. The reaction involves sodium methoxide (NaOCH₃) and acetic acid (CH₃COOH) as reactants. 3. **Figure (g):** - The compound is a cycloalkane with a chlorine group (Cl) and two methyl groups at the adjacent carbon. The reaction involves heating with sulfuric acid (H₂SO₄). 4. **Figure (h):** - The structure here is a linear alkane with a chlorine substituent. The reaction involves heating with phosphoric acid (H₃PO₄). #### Process Overview - **Heating and Acid Catalysts:** Each reaction involves heating the compound in the presence of an acid, which is a common method to facilitate elimination reactions leading to dehydration or dehydrohalogenation. - **Common Outcomes:** - **Dehydration (e and h):** Likely leads to the loss of a water molecule, resulting in an alkene. - **Dehydrohalogenation (f and g):** Likely results in the removal of a hydrogen and a halogen, forming an alkene. These reactions are typical examples of organic transformation processes used in synthesis and provide insight into mechanisms like elimination and substitution.
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