HBr - А NACN В HCI/H2O C SOC). D- E H2O2

Chemistry
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Give the major organic product(s) for each step of the following reaction
### Organic Chemistry Reaction Pathway

This diagram illustrates a multi-step organic reaction pathway beginning with an alkene and ending with an acyl chloride. The steps in the reaction and the reagents used at each step are detailed as follows:

1. **Starting Material**: 2-Butene (CH3-CH=CH-CH3)
2. **Step 1**:
   - *Reagents*: HBr (Hydrobromic Acid) and H2O2 (Hydrogen Peroxide)
   - *Product A*: Bromoalkane
   - *Description*: This step likely involves an anti-Markovnikov addition of HBr to the alkene in the presence of peroxide (H2O2), leading to the formation of 1-Bromobutane (CH3-CH2-CH2-CH2Br).

3. **Step 2**:
   - *Reagent*: NaCN (Sodium Cyanide)
   - *Product B*: Nitrile compound
   - *Description*: In this step, a nitrile group (CN) is introduced by reacting the bromoalkane with sodium cyanide, producing butanenitrile (CH3-CH2-CH2-CH2CN).

4. **Step 3**:
   - *Reagent*: HCl (Hydrochloric Acid) in H2O (Water)
   - *Product C*: Carboxylic Acid
   - *Description*: This step converts the nitrile to a carboxylic acid by hydrolysis, yielding butanoic acid (CH3-CH2-CH2-COOH).

5. **Step 4**:
   - *Reagent*: SOCl2 (Thionyl Chloride)
   - *Product D*: Acyl Chloride
   - *Product Structure*: 
        ```
        O
        ||
        C-Cl
        ```
   - *Description*: This reaction transforms the carboxylic acid into its acyl chloride derivative, producing butanoyl chloride (CH3-CH2-CH2-COCl).

6. **Step 5**: 
   - *Product E*: Final Product – the diagram does not provide details on the final product.

### Diagram Explanation:
The diagram provides a visual representation of the change in the chemical structure at each step.

1. Starting from an alkene (double bond between carbon atoms).
2. Adding H
Transcribed Image Text:### Organic Chemistry Reaction Pathway This diagram illustrates a multi-step organic reaction pathway beginning with an alkene and ending with an acyl chloride. The steps in the reaction and the reagents used at each step are detailed as follows: 1. **Starting Material**: 2-Butene (CH3-CH=CH-CH3) 2. **Step 1**: - *Reagents*: HBr (Hydrobromic Acid) and H2O2 (Hydrogen Peroxide) - *Product A*: Bromoalkane - *Description*: This step likely involves an anti-Markovnikov addition of HBr to the alkene in the presence of peroxide (H2O2), leading to the formation of 1-Bromobutane (CH3-CH2-CH2-CH2Br). 3. **Step 2**: - *Reagent*: NaCN (Sodium Cyanide) - *Product B*: Nitrile compound - *Description*: In this step, a nitrile group (CN) is introduced by reacting the bromoalkane with sodium cyanide, producing butanenitrile (CH3-CH2-CH2-CH2CN). 4. **Step 3**: - *Reagent*: HCl (Hydrochloric Acid) in H2O (Water) - *Product C*: Carboxylic Acid - *Description*: This step converts the nitrile to a carboxylic acid by hydrolysis, yielding butanoic acid (CH3-CH2-CH2-COOH). 5. **Step 4**: - *Reagent*: SOCl2 (Thionyl Chloride) - *Product D*: Acyl Chloride - *Product Structure*: ``` O || C-Cl ``` - *Description*: This reaction transforms the carboxylic acid into its acyl chloride derivative, producing butanoyl chloride (CH3-CH2-CH2-COCl). 6. **Step 5**: - *Product E*: Final Product – the diagram does not provide details on the final product. ### Diagram Explanation: The diagram provides a visual representation of the change in the chemical structure at each step. 1. Starting from an alkene (double bond between carbon atoms). 2. Adding H
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