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

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter20: Acidity And Pka Of Phenols
Section: Chapter Questions
Problem 11E
icon
Related questions
icon
Concept explainers
Question
### 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.
Expert Solution
steps

Step by step

Solved in 2 steps with 2 images

Blurred answer
Knowledge Booster
Lipids
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Organic Chemistry: A Guided Inquiry
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:
9780618974122
Author:
Andrei Straumanis
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9781305580350
Author:
William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:
Cengage Learning