Mechanisms. Give the curved-arrow mechanism for each reaction indicated below. Use and attach extra sheets as needed, in order. H+ a H. NH2 H. H+ HN .CI Cl2 hv

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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### Mechanisms

#### Curved-Arrow Mechanisms of Reactions

For each reaction below, provide the detailed curved-arrow mechanism. Attach extra sheets as needed to thoroughly explain each step.

#### Reaction a
![Reaction a](img_a)
- **Reactants**: An aldehyde and propylamine (C₃H₇NH₂).
- **Conditions**: Presence of an acid catalyst (H⁺).
- **Products**: Formation of an imine.

#### Reaction b
![Reaction b](img_b)
- **Reactants**: A cyclic ketone and ethylene diamine (C₂H₅N₂).
- **Conditions**: Presence of an acid catalyst (H⁺).
- **Products**: Formation of a cyclic imine.

#### Reaction c
![Reaction c](img_c)
- **Reactants**: Cyclohexane.
- **Conditions**: Exposure to chlorine (Cl₂) and light (hv).
- **Products**: Formation of chlorocyclohexane.

### Instructions
- Explain each step of the reaction, depicting all intermediates and transition states.
- Use curved-arrow notation to indicate electron movement.
- Include extra sheets to provide detailed mechanisms if necessary.
Transcribed Image Text:### Mechanisms #### Curved-Arrow Mechanisms of Reactions For each reaction below, provide the detailed curved-arrow mechanism. Attach extra sheets as needed to thoroughly explain each step. #### Reaction a ![Reaction a](img_a) - **Reactants**: An aldehyde and propylamine (C₃H₇NH₂). - **Conditions**: Presence of an acid catalyst (H⁺). - **Products**: Formation of an imine. #### Reaction b ![Reaction b](img_b) - **Reactants**: A cyclic ketone and ethylene diamine (C₂H₅N₂). - **Conditions**: Presence of an acid catalyst (H⁺). - **Products**: Formation of a cyclic imine. #### Reaction c ![Reaction c](img_c) - **Reactants**: Cyclohexane. - **Conditions**: Exposure to chlorine (Cl₂) and light (hv). - **Products**: Formation of chlorocyclohexane. ### Instructions - Explain each step of the reaction, depicting all intermediates and transition states. - Use curved-arrow notation to indicate electron movement. - Include extra sheets to provide detailed mechanisms if necessary.
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