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6.17 Mechanism of Halogen Addition to Alkenes: Halonium Ions

6.17 Mechanism of Halogen Addition to Alkenes: Halonium Ions. Mechanism is electrophilic addition. Br 2 is not polar, but it is polarizable two steps involved (1) formation of bromonium ion (2) nucleophilic attack on bromonium ion by bromide. Relative Rates. Bromination.

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990 views • 77 slides

Chapter 17: Aldehydes and Ketones: Nucleophilic Addition to the Carbonyl Group

Chapter 17: Aldehydes and Ketones: Nucleophilic Addition to the Carbonyl Group 17.1: Nomenclature (please read) 17.2: Structure and Bonding: Carbonyl groups have a significant dipole moment. Aldehyde 2.72 D Ketone 2.88 Carboxylic acid 1.74 Acid chloride 2.72 Ester 1.72

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720 views • 29 slides

Methods

Delete me & place your LOGO in this area. Studying the Temperature Effect on Yield and Rate Of the Epoxidation of Cyclohexene Chris Lewis and Dr. David Oostendorp , PHD Loras College Molecular Life Science. BACKGROUND. MATERIALS AND METHODS. RESULTS.

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125 views • 1 slides

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Peroxy acid - PowerPoint PPT Presentation

6.17 Mechanism of Halogen Addition to Alkenes: Halonium Ions

Chapter 17: Aldehydes and Ketones: Nucleophilic Addition to the Carbonyl Group

Methods